ENSMUSG00000025219


Mus musculus

Features
Gene ID: ENSMUSG00000025219
  
Biological name :Fgf8
  
Synonyms : Fgf8 / Fibroblast growth factor 8 / P37237
  
Possible biological names infered from orthology : P55075
  
Species: Mus musculus
  
Chr. number: 19
Strand: -1
Band: C3
Gene start: 45736798
Gene end: 45742915
  
Corresponding Affymetrix probe sets: 10468070 (MoGene1.0st)   1451882_a_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000107558
Ensembl peptide - ENSMUSP00000107556
Ensembl peptide - ENSMUSP00000107559
Ensembl peptide - ENSMUSP00000026240
Ensembl peptide - ENSMUSP00000026241
Ensembl peptide - ENSMUSP00000107555
NCBI entrez gene - 14179     See in Manteia.
MGI - MGI:99604
RefSeq - XM_011247143
RefSeq - NM_001166361
RefSeq - NM_001166362
RefSeq - NM_001166363
RefSeq - NM_010205
RefSeq - XM_006526668
RefSeq - XM_011247142
RefSeq Peptide - NP_001159834
RefSeq Peptide - NP_001159835
RefSeq Peptide - NP_034335
RefSeq Peptide - NP_001159833
swissprot - P37237
swissprot - Q3V279
swissprot - Q80ZL6
swissprot - D3Z207
swissprot - D3Z208
Ensembl - ENSMUSG00000025219
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 FGF8ENSGALG00000007706Gallus gallus
 FGF8ENSG00000107831Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Fgf17 / P63075 / Fibroblast growth factor 17 / O60258*ENSMUSG0000002210146
Fgf18 / O89101 / Fibroblast growth factor 18 / O76093*ENSMUSG0000005796735


Protein motifs (from Interpro)
Interpro ID Name
 IPR002209  Fibroblast growth factor family
 IPR008996  Cytokine IL1/FGF
 IPR028249  Fibroblast growth factor 8


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0000165 MAPK cascade IMP
 biological_processGO:0001569 branching involved in blood vessel morphogenesis IGI
 biological_processGO:0001656 metanephros development IEA
 biological_processGO:0001658 branching involved in ureteric bud morphogenesis IMP
 biological_processGO:0001759 organ induction IGI
 biological_processGO:0001822 kidney development IMP
 biological_processGO:0001823 mesonephros development IEA
 biological_processGO:0001839 neural plate morphogenesis IMP
 biological_processGO:0001947 heart looping IMP
 biological_processGO:0001974 blood vessel remodeling IGI
 biological_processGO:0003007 heart morphogenesis IMP
 biological_processGO:0003148 outflow tract septum morphogenesis IGI
 biological_processGO:0003151 outflow tract morphogenesis IGI
 biological_processGO:0003198 epithelial to mesenchymal transition involved in endocardial cushion formation IMP
 biological_processGO:0006915 apoptotic process IMP
 biological_processGO:0007275 multicellular organism development IEA
 biological_processGO:0007368 determination of left/right symmetry IMP
 biological_processGO:0007507 heart development IMP
 biological_processGO:0008078 mesodermal cell migration IMP
 biological_processGO:0008284 positive regulation of cell proliferation ISO
 biological_processGO:0008406 gonad development ISO
 biological_processGO:0008543 fibroblast growth factor receptor signaling pathway IEA
 biological_processGO:0009792 embryo development ending in birth or egg hatching IMP
 biological_processGO:0010469 regulation of signaling receptor activity IEA
 biological_processGO:0010628 positive regulation of gene expression IMP
 biological_processGO:0021537 telencephalon development IMP
 biological_processGO:0021543 pallium development IMP
 biological_processGO:0021544 subpallium development IMP
 biological_processGO:0021798 forebrain dorsal/ventral pattern formation IMP
 biological_processGO:0021846 cell proliferation in forebrain IMP
 biological_processGO:0023019 signal transduction involved in regulation of gene expression IDA
 biological_processGO:0030154 cell differentiation IEA
 biological_processGO:0030324 lung development IMP
 biological_processGO:0030509 BMP signaling pathway IDA
 biological_processGO:0030539 male genitalia development IDA
 biological_processGO:0030878 thyroid gland development IMP
 biological_processGO:0030916 otic vesicle formation TAS
 biological_processGO:0030917 midbrain-hindbrain boundary development IMP
 biological_processGO:0035050 embryonic heart tube development IMP
 biological_processGO:0035108 limb morphogenesis IGI
 biological_processGO:0035116 embryonic hindlimb morphogenesis IGI
 biological_processGO:0035909 aorta morphogenesis IGI
 biological_processGO:0042472 inner ear morphogenesis IGI
 biological_processGO:0042476 odontogenesis IEA
 biological_processGO:0042487 regulation of odontogenesis of dentin-containing tooth IGI
 biological_processGO:0043066 negative regulation of apoptotic process IMP
 biological_processGO:0043524 negative regulation of neuron apoptotic process IMP
 biological_processGO:0045165 cell fate commitment IGI
 biological_processGO:0045840 positive regulation of mitotic nuclear division IDA
 biological_processGO:0046622 positive regulation of organ growth IMP
 biological_processGO:0048699 generation of neurons IMP
 biological_processGO:0048853 forebrain morphogenesis IMP
 biological_processGO:0051781 positive regulation of cell division IEA
 biological_processGO:0055026 negative regulation of cardiac muscle tissue development ISO
 biological_processGO:0060037 pharyngeal system development IGI
 biological_processGO:0060070 canonical Wnt signaling pathway IDA
 biological_processGO:0060128 corticotropin hormone secreting cell differentiation IDA
 biological_processGO:0060129 thyroid-stimulating hormone-secreting cell differentiation IDA
 biological_processGO:0060348 bone development ISO
 biological_processGO:0060425 lung morphogenesis IMP
 biological_processGO:0060445 branching involved in salivary gland morphogenesis IMP
 biological_processGO:0060563 neuroepithelial cell differentiation ISO
 biological_processGO:0070374 positive regulation of ERK1 and ERK2 cascade IGI
 biological_processGO:0071542 dopaminergic neuron differentiation TAS
 biological_processGO:0090134 cell migration involved in mesendoderm migration IMP
 cellular_componentGO:0005576 extracellular region IEA
 cellular_componentGO:0005615 extracellular space ISO
 cellular_componentGO:0005622 intracellular IEA
 molecular_functionGO:0005104 fibroblast growth factor receptor binding IEA
 molecular_functionGO:0005105 type 1 fibroblast growth factor receptor binding ISO
 molecular_functionGO:0005111 type 2 fibroblast growth factor receptor binding ISO
 molecular_functionGO:0008083 growth factor activity IEA


Pathways (from Reactome)
Pathway description
PI3K Cascade
PIP3 activates AKT signaling
FGFR4 ligand binding and activation
FGFR3b ligand binding and activation
FGFR3c ligand binding and activation
FGFR1c ligand binding and activation
FGFR2c ligand binding and activation
Phospholipase C-mediated cascade: FGFR1
Phospholipase C-mediated cascade; FGFR2
Phospholipase C-mediated cascade; FGFR3
Phospholipase C-mediated cascade; FGFR4
Downstream signaling of activated FGFR1
SHC-mediated cascade:FGFR1
PI-3K cascade:FGFR1
FRS-mediated FGFR1 signaling
PI-3K cascade:FGFR2
SHC-mediated cascade:FGFR2
FRS-mediated FGFR2 signaling
SHC-mediated cascade:FGFR3
FRS-mediated FGFR3 signaling
PI-3K cascade:FGFR3
FRS-mediated FGFR4 signaling
SHC-mediated cascade:FGFR4
PI-3K cascade:FGFR4
Negative regulation of FGFR1 signaling
Negative regulation of FGFR2 signaling
Negative regulation of FGFR3 signaling
Negative regulation of FGFR4 signaling
FGFRL1 modulation of FGFR1 signaling
RAF/MAP kinase cascade
PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000018 small ears "outer ears of a smaller than normal size" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Gbx2tm1.1Mrt/Gbx2+,Fgf8tm1.4Mrt/Fgf8+
Genetic Background: B6.129-Gbx2tm1.1Mrt Fgf8tm1.4Mrt

 MP:0000266 abnormal cardiac morphology "anomalies in the hollow, muscular organ that maintains the circulation of the blood" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Nkx2-5tm1(cre)Rjs/Nkx2-5+
Genetic Background: involves: 129P2/OlaHsd * 129S7/SvEvBrd

 MP:0000267 abnormal cardiac development "aberrant formation or incomplete differentiation of the heart" [MGI:cls, J:53370]
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Allelic Composition: Fgf4tm1.2Mrt/Fgf4tm1.3Mrt,Tg(Msx2-cre)5Rem/0
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(Tbx1-cre)1Joe/0
Genetic Background: Not Specified

Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm2Mrt,Nkx2-5tm1(cre)Rjs/Nkx2-5+
Genetic Background: involves: 129 * 129S7/SvEvBrd

Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sortm1Sor,Nkx2-5tm1(cre)Rjs/Nkx2-5+
Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJaeSor * 129S7/SvEvBrd

 MP:0000270 abnormal heart tube morphology "malformed embryonic heart " [J:37888]
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Allelic Composition: Dad1tm1Brw/Dad1tm1Brw
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Nkx2-5tm1(cre)Rjs/Nkx2-5+
Genetic Background: involves: 129P2/OlaHsd * 129S7/SvEvBrd

Allelic Composition: Fgf8tm1.1Jyhl/Fgf8tm1.1Jyhl
Genetic Background: involves: CD-1

 MP:0000284 double outlet right ventricle "both the aorta and the pulmonary trunk originate from the right ventricle, usually in conjunction with a ventricular septal defect" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:67826]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(Tbx1-cre)1Joe/0
Genetic Background: Not Specified

Allelic Composition: Fgf8tm2Moon/Fgf8tm1Mrc,Tg(Mef2c-cre)2Blk/0
Genetic Background: Not Specified

Allelic Composition: Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10+,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

 MP:0000352 decreased cell proliferation "less than the normal growth and reproduction of similar cells" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Dad1tm1Brw/Dad1tm1Brw
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

 MP:0000428 abnormal craniofacial morphology "anomalous structure or development of the face and/or cranium" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm3Mrc
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Del(19Poll-Fbxw4)4Fsp/+,Fgf8tm1.4Mrt/Fgf8+
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv

 MP:0000455 abnormal maxilla morphology "malformation of the upper bony framework of the mouth where the superior teeth are held" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

 MP:0000458 abnormal mandible morphology "malformation of the lower bony framework of the mouth where the inferior teeth are held" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

 MP:0000520 absent kidney "missing paired organs that excrete urine" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49471]
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Allelic Composition: Del(19Poll-Fbxw4)4Fsp/+,Fgf8tm1.4Mrt/Fgf8+
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv

 MP:0000527 abnormal kidney development "anomalous differentiation of the paired organs responsible for urine secretion" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(T-cre)1Lwd/0
Genetic Background: involves: 129P2/OlaHsd * C3H * C57BL/6 * CD-1

 MP:0000547 short limbs "reduced average length of the extremities" [MGI:CLS, J:61509]
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Allelic Composition: Del(19Poll-Fbxw4)4Fsp/+,Fgf8tm1.4Mrt/Fgf8+
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv

 MP:0000551 absent forelimb "missing the entire anterior extremities" [MGI:tc, J:54637]
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Allelic Composition: Del(19Poll-Fbxw4)4Fsp/+,Fgf8tm1.4Mrt/Fgf8+
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv

 MP:0000553 absent radius "missing the short bone of the lateral forearm" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:54637]
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Allelic Composition: Grm1tm1Stl/Grm1tm1Stl
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0000557 absent hindlimb "missing the entire posterior extremities" [MGI:tc, J:54637]
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Allelic Composition: Del(19Poll-Fbxw4)4Fsp/+,Fgf8tm1.4Mrt/Fgf8+
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv

 MP:0000564 syndactyly "any degree of webbing or fusion of the digits, may involve only soft tissues or also can include bone" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Fgf4tm1.2Mrt/Fgf4tm1.3Mrt,Tg(Msx2-cre)5Rem/0
Genetic Background: involves: 129P2/OlaHsd

 MP:0000565 oligodactyly "congenital condition in which some digits or parts of digits are missing" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:53370]
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Allelic Composition: Grm1tm1Stl/Grm1tm1Stl
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(T-cre)1Lwd/0
Genetic Background: involves: 129P2/OlaHsd * C3H * C57BL/6 * CD-1

 MP:0000633 abnormal pituitary gland morphology "anomalous structure of the compound gland suspended from the base of the hypothalamus, which secretes somatotropins, prolactin, TSH (thyroid-stimulating hormone), gonadotropins, adrenal corticotropin" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Fgf4tm1.2Mrt/Fgf4tm1.3Mrt,Tg(Msx2-cre)5Rem/0
Genetic Background: involves: 129P2/OlaHsd

 MP:0000678 abnormal parathyroid gland morphology "anomalous structure of one of the two small, paired endocrine glands, usually found embedded in the connective tissue capsule on the posterior surface of the thyroid gland; they secrete parathyroid hormone (PTH) that regulates calcium and phosphorous metabolism" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0000680 absent parathyroid glands "missing the two small, paired endocrine glands, usually found embedded in the connective tissue capsule on the posterior surface of the thyroid gland, which secrete parathyroid hormone (PTH) " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0000703 abnormal thymus morphology "anomalous structure or development of the primary lymphoid organ; required for immune system development" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:55400]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(Tbx1-cre)1Joe/0
Genetic Background: Not Specified

 MP:0000704 abnormal thymus development "anomaly in the formation and/or differentiation of the thymus" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Gbx2tm1.1Mrt/Gbx2+,Fgf8tm1.4Mrt/Fgf8+
Genetic Background: B6.129-Gbx2tm1.1Mrt Fgf8tm1.4Mrt

 MP:0000706 small thymus "reduced size of the thymus" [J:36561, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, J:31167]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(Tbx1-cre)1Joe/0
Genetic Background: Not Specified

 MP:0000836 abnormal substantia nigra morphology "malformation or absence of the layer of gray substance that separates the posterior parts of the cerebral peduncles (tegmentum mesencephali) from the anterior parts; it normally includes a posterior compact part with many pigmented cells (pars compacta) and an anterior reticular part whose cells contain little pigment (pars reticularis)" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: En1tm7(cre/ESR1)Alj/0,Fgf8tm1.1Jyhl/Fgf8tm1.3Mrt
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac

Allelic Composition: En1tm7(cre/ESR1)Alj/0,Fgf8tm1.3Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac

 MP:0000837 abnormal hypothalamus morphology "any malformation or absence of the ventral part of the diencephalon extending from the region of the optic chiasm to the caudal border of the mammillary bodies and forming the inferior and lateral walls of the third ventricle; this region regulates the autonomic nervous system via hormone production and release" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Fgf8tm1.1Mrt/Fgf8tm1.2Mrt
Genetic Background: involves: 129P2/OlaHsd

 MP:0000850 absent cerebellum "missing the part of the metencephalon that lies in the posterior cranial fossa dorsal to the pons and medulla that is concerned with the coordination of movement" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:19212, MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Fgf4tm1.2Mrt/Fgf4tm1.3Mrt,Tg(Msx2-cre)5Rem/0
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.1Mrt/Fgf8tm1.2Mrt
Genetic Background: involves: 129P2/OlaHsd

 MP:0000852 small cerebellum "reduced size of cerebellum" [MGI:CLS, J:17203, J:67524]
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Allelic Composition: En1tm7(cre/ESR1)Alj/0,Fgf8tm1.1Jyhl/Fgf8tm1.3Mrt
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac

Allelic Composition: En1tm7(cre/ESR1)Alj/0,Fgf8tm1.3Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac

 MP:0000864 abnormal vermis "malformation in the narrow middle zone between the two hemispheres of the cerebellum" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61509]
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Allelic Composition: Fgf8tm1.4Mrt/Fgf8+,Fgf17tm1Dor/Fgf17tm1Dor
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac

 MP:0000867 abnormal anterior vermis "malformation in the anterior portion of the narrow middle zone between the two hemispheres of the cerebellum" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61509]
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Allelic Composition: Fgf8tm1.4Mrt/Fgf8+,Fgf17tm1Dor/Fgf17tm1Dor
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac

Allelic Composition: Fgf17tm1Dor/Fgf17tm1Dor,Fgf8tm1.1Jyhl/Fgf8tm1.1Jyhl
Genetic Background: involves: 129S6/SvEvTac

 MP:0000877 abnormal Purkinje cell "any structural anomaly of the neurons located at the interface of the molecular and internal granule layers of the cerebellar cortex; these inhibitory neurons provide the output of the cerebellar cortex through axons that project into the white matter, and extensive dendritic trees from the Purkinje cells extend upward in a single plane into the molecular layer where they synapse with parallel fibers of granule cells" [J:46140, Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3]
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Allelic Composition: Cd80tm1Lbgn/Cd80tm1Lbgn
Genetic Background: C3.Cg-Cd80tm1Lbgn

 MP:0000897 abnormal midbrain "malformation or malfunction associated with the middle of the three cerebral vesicles of the embryo; this region controls sensory and motor functions, including eye movement and coordination of auditory and visual reflexes" [J:23882, Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3]
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Allelic Composition: Fgf8tm1.1Mrt/Fgf8tm1.2Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: En1tm7(cre/ESR1)Alj/0,Fgf8tm1.1Jyhl/Fgf8tm1.3Mrt
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac

Allelic Composition: En1tm7(cre/ESR1)Alj/0,Fgf8tm1.3Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac

 MP:0000913 abnormal brain development "malformed or incomplete differentiation of the brain" [MGI:cls, J:49840]
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Allelic Composition: Del(19Poll-Fbxw4)4Fsp/+,Fgf8tm1.4Mrt/Fgf8+
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv

 MP:0000929 open neural tube "incomplete invagination and fusion of the neuroepithelial layer in early development" [MGI:CLS, J:53370, J:62571]
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Allelic Composition: Fgf8tm1.1Jyhl/Fgf8tm1.1Jyhl
Genetic Background: involves: CD-1

 MP:0000933 abnormal rhombomere morphology "malformation of the transverse segments in the hindbrain region of the developing neural tube" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:1776]
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Allelic Composition: Aicdatm1Hon/Aicdatm1Hon,Ighmtm1.1(IGH-2)Cog/Ighm+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * CBA * FVB/N

 MP:0000936 small telencephalic vesicles "reduced size of the paired diverticula of the telencephalon, from which the forebrain develops" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:49840]
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Allelic Composition: Fgf8tm1.1Mrt/Fgf8tm1.2Mrt
Genetic Background: involves: 129P2/OlaHsd

 MP:0001065 abnormal trigeminal nerve morphology "malformed chief sensory nerve of the face and motor nerve of the muscles of mastication; has three major divisions: ophthalmic, maxillary and mandibular " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, Principles of Neural Science:ISBN 0-8385-8034-3, J:33038]
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Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

 MP:0001262 decreased body weight "lower than normal average weight " [J:61295]
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Allelic Composition: En1tm7(cre/ESR1)Alj/0,Fgf8tm1.3Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac

Allelic Composition: Fgf8tm2.1Jyhl/Fgf8+
Genetic Background: B6.129S6-Fgf8tm2.1Jyhl

 MP:0001340 abnormal eyelid morphology "malformation of the skin folds covering the front of the eyeball" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: cir/cir+,Tmiesr/Tmie+
Genetic Background: involves: C57BL/6J * C57BL/How * ICR

 MP:0001406 abnormal gait "unusual or distinctive way of walking" [J:65038]
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Allelic Composition: Cd80tm1Lbgn/Cd80tm1Lbgn
Genetic Background: C3.Cg-Cd80tm1Lbgn

 MP:0001575 cyanosis "a dark bluish or purple skin discoloration resulting from deficient oxygenation of the blood" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60159]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm3Mrc
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0001614 abnormal vasculature "anomalies in the structure of development of the network of tubes that carries blood through the body" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0001675 abnormal ectoderm development "failure or abnormality in the formation of the ectoderm during gastrulation" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Fgf4tm1.2Mrt/Fgf4tm1.3Mrt,Tg(Msx2-cre)5Rem/0
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.4Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

 MP:0001680 abnormal mesoderm development "failure or abnormality in the formation of the mesoderm during gastrulation" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Fgf4tm1.2Mrt/Fgf4tm1.3Mrt,Tg(Msx2-cre)5Rem/0
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.4Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1Jyhl/Fgf8tm1Jyhl
Genetic Background: involves: CD-1

Allelic Composition: Fgf8tm1.1Jyhl/Fgf8tm1.1Jyhl
Genetic Background: involves: CD-1

 MP:0001683 absent mesoderm "missing or failure to differentiate the middle primary germ layer " [J:40594]
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Allelic Composition: Fgf8tm1Jyhl/Fgf8tm1Jyhl
Genetic Background: involves: CD-1

 MP:0001688 abnormal somite development "anomalous formation of any of the paired, metamerically arranged cell masses formed in the embryonic paraxial mesoderm" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Fgf8tm1Jyhl/Fgf8tm1Jyhl
Genetic Background: involves: CD-1

 MP:0001698 reduced embryo size "smaller proportions of embryo compared to littermates" [J:61790]
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Allelic Composition: Fgf4tm1.2Mrt/Fgf4tm1.3Mrt,Tg(Msx2-cre)5Rem/0
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.1Mrt/Fgf8tm1.2Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.1Jyhl/Fgf8tm1.1Jyhl
Genetic Background: involves: CD-1

 MP:0001726 abnormal allantois "malformed fetal membrane which contributes to the formation of the umbilical cord and placenta" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:12622]
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Allelic Composition: Fgf4tm1.2Mrt/Fgf4tm1.3Mrt,Tg(Msx2-cre)5Rem/0
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.4Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

 MP:0001732 postnatal growth retardation "slow or limited development after birth " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: cir/cir+,Tmiesr/Tmie+
Genetic Background: involves: C57BL/6J * C57BL/How * ICR

 MP:0001785 edema "an accumulation of an excessive amount of watery fluid in cells or intercellular tissues" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:54065]
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Allelic Composition: Dad1tm1Brw/Dad1tm1Brw
Genetic Background: involves: 129P2/OlaHsd * Black Swiss

Allelic Composition: Fgf8tm1Mrc/Fgf8tm3Mrc
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0001823 thymus hypoplasia "small size due to reduced cell number in the thymus" [J:23255]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1.4Mrt/Fgf8+,Tbx1tm1Bld/Tbx1+
Genetic Background: involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * ICR

 MP:0002080 prenatal lethality "death anytime between fertilization and E18.5" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Grm1tm1Stl/Grm1tm1Stl
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0002082 postnatal lethality "premature death anytime after postnatal day 1 to weaning age (3 weeks)" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: En1tm7(cre/ESR1)Alj/0,Fgf8tm1.3Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac

 MP:0002084 abnormal developmental patterning "abnormal systematic arrangement of the developing body along an axis" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm1Jyhl/Fgf8tm1Jyhl
Genetic Background: involves: CD-1

 MP:0002109 abnormal limb morphology "abnormal development of limbs resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm2Mrc/Fgf8tm2Mrc
Genetic Background: Not Specified

 MP:0002110 abnormal digit morphology "abnormal development of the digits resulting in structural abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm2Mrc/Fgf8tm2Mrc
Genetic Background: Not Specified

 MP:0002115 abnormal skeleton extremities morphology "abnormal development of limb, foot or tail bones resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm2Mrc/Fgf8tm2Mrc
Genetic Background: Not Specified

 MP:0002127 abnormal cardiovascular system morphology "abnormal development of the heart or vascular tissue resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Cdkn1btm1Mlf/Cdkn1btm1Mlf,Trp53tm1Brd/Trp53tm1Brd
Genetic Background: involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6J

Allelic Composition: Fgf8tm1Mrc/Fgf8tm3Mrc
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0002151 abnormal neural tube morphology/development "anomalous structure of or development of the embryonic neural tube resulting in structural anomaly" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Aicdatm1Hon/Aicdatm1Hon,Ighmtm1.1(IGH-2)Cog/Ighm+
Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * CBA * FVB/N

 MP:0002152 abnormal brain morphology "anomalous structure of or abnormal development of the brain, one of the two components of the central nervous system and the center of thought and emotion; controls coordination, bodily activities and the interpretation of information from the senses (sight, hearing, smell, etc.)" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, http://cancerweb.ncl.ac.uk]
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Allelic Composition: Del(19Poll-Fbxw4)4Fsp/+,Fgf8tm1.4Mrt/Fgf8+
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv

 MP:0002160 abnormal reproductive system morphology "structural or developmental anomaly of any of the tissues involved in the reproductive system" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: cir/cir+,Tmiesr/Tmie+
Genetic Background: involves: C57BL/6J * C57BL/How * ICR

 MP:0002169 no phenotype detected "normal, viable and fertile appearance and behavior; indistinguishable from controls" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm1.1Mrt/Fgf8tm1.2Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.3Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc
Genetic Background: Not Specified

Allelic Composition: Fgf8tm2Mrc/Fgf8tm2Mrc
Genetic Background: Not Specified

Allelic Composition: Fgf8tm1(cre)Itl/Fgf8+
Genetic Background: Not Specified

 MP:0002231 abnormal primitive streak morphology "anomaly in the midline ridge of the embryonic epiblast that later develops into mesoderm and endoderm" [The Atlas of Mouse Development:ISBN 0-12-402035-6, csmith:Cynthia L. Smith, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm1Jyhl/Fgf8tm1Jyhl
Genetic Background: involves: CD-1

Allelic Composition: Fgf8tm1.1Jyhl/Fgf8tm1.1Jyhl
Genetic Background: involves: CD-1

 MP:0002633 persistent truncus arteriosis "complete failure of the common arterial trunk opening out of both ventricles to divide into the aorta and pulmonary artery during development" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(Tbx1-cre)1Joe/0
Genetic Background: Not Specified

Allelic Composition: Fgf8tm2Moon/Fgf8tm1Mrc,Isl1tm1(cre)Sev/Isl1+
Genetic Background: involves: 129S/Sv

Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Moon,Isl1tm1(cre)Sev/Isl1+
Genetic Background: involves: 129S/Sv * Black Swiss * C57BL/6

 MP:0002672 abnormal branchial arch artery morphology "malformation of the vessels formed within the five pairs of branchial arches in embryogenesis; in the adult, some of these vessels give rise to the great vessels" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Gbx2tm1.1Mrt/Gbx2+,Fgf8tm1.4Mrt/Fgf8+
Genetic Background: B6.129-Gbx2tm1.1Mrt Fgf8tm1.4Mrt

Allelic Composition: Gbx2tm1.1Mrt/Gbx2tm1.1Mrt,Fgf8tm1.4Mrt/Fgf8+
Genetic Background: B6.129-Gbx2tm1.1Mrt Fgf8tm1.4Mrt

Allelic Composition: Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10+,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

 MP:0002753 dilated left ventricle "an expansion in the volume of the lower left chamber of the heart" [J:82859, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Nkx2-5tm1(cre)Rjs/Nkx2-5+
Genetic Background: involves: 129P2/OlaHsd * 129S7/SvEvBrd

 MP:0002836 abnormal chorion "malformations of the outermost extraembryonic membrane" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Fgf4tm1.2Mrt/Fgf4tm1.3Mrt,Tg(Msx2-cre)5Rem/0
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.4Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

 MP:0002884 abnormal branchial arches "malformation or anomaly in the transient structures of the embryo that develop into regions of the head, neck and ears" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm2Mrt,Nkx2-5tm1(cre)Rjs/Nkx2-5+
Genetic Background: involves: 129 * 129S7/SvEvBrd

Allelic Composition: Fgf8tm1.1Jyhl/Fgf8tm1.1Jyhl
Genetic Background: involves: CD-1

 MP:0002925 abnormal cardiovascular development "aberrant formation or incomplete differentiation of the cardiovascular system" [RGD:Rat Genome Database submission]
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Allelic Composition: Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10+,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

 MP:0002950 abnormal neural crest cell migration "defect in the dispersion of the transient and migratory group of cells that emerge from the dorsal region of the neural tube and migrate to many peripheral locations to form various tissues of the adult" [Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3]
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Allelic Composition: Gbx2tm1.1Mrt/Gbx2tm1.1Mrt,Fgf8tm1.4Mrt/Fgf8+
Genetic Background: B6.129-Gbx2tm1.1Mrt Fgf8tm1.4Mrt

 MP:0003007 ectopic thymus "ectopic location of the thymus primordium, which normally resides in the superior mediastinum and lower part of the neck" [ava:Anna V. Anagnostopoulos , Mouse Genome Informatics Curator, J:76015]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0003140 dilated atria "an expansion in the volume of one or both of the upper chambers of the heart" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Nkx2-5tm1(cre)Rjs/Nkx2-5+
Genetic Background: involves: 129P2/OlaHsd * 129S7/SvEvBrd

 MP:0003152 abnormal pillar cell differentiation "abnormal differentiation of the supporting cells that form the inner and outer walls of the tunnel in the organ of Corti" [J:32991, anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator]
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Allelic Composition: Pdyntm1Zim/Pdyntm1Zim
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0003202 abnormal neuron apoptosis "change in the timing or the number of neurons undergoing programmed cell death" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Hey2tm1Mtc/Hey2tm1Mtc
Genetic Background: C.Cg-Hey2tm1Mtc

 MP:0003203 increased neuron apoptosis "increase in the number of neurons undergoing programmed cell death" [RGD:Rat Genome Database submission]
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Allelic Composition: Hey2tm1Mtc/Hey2tm1Mtc
Genetic Background: C.Cg-Hey2tm1Mtc

Allelic Composition: Fgf8tm1.1Mrt/Fgf8tm1.4Mrt,Foxg1tm1(cre)Skm/Foxg1+
Genetic Background: involves: 129P2/OlaHsd

 MP:0003204 decreased neuron apoptosis "decrease in the number of neurons undergoing programmed cell death" [RGD:Rat Genome Database submission]
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Allelic Composition: Airntm1Dpb/Airn+
Genetic Background: involves: FVB/N

 MP:0003232 abnormal forebrain development "anomaly in the formation or patterning of the anterior primitive cerebral vesicle; most rostral of three primary vesicles of the embryonic neural tube" [J:93081, smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Pdyntm1Zim/Pdyntm1Zim
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0003308 abnormal cochlear sensory epithelium 
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Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.3Mrt,Foxg1tm1(cre)Skm/Foxg1+
Genetic Background: involves: 129P2/OlaHsd

 MP:0003395 abnormal subclavian artery morphology "malformation of the right or left subclavian arteries, The right subclavian artery extends from the brachiocephalic artery to the right side of the body. The left subclavian artery extends from the aortic arch to the left side of the body." [ncbi:Matthew Mailman, NCBI request, smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0003451 absent olfactory bulb "absence of the forebrain region that coordinates neuronal signaling involved in the perception of smell; it receives input from the sensory neurons and outputs to the olfactory cortex" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Fgf4tm1.2Mrt/Fgf4tm1.3Mrt,Tg(Msx2-cre)5Rem/0
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Del(19Poll-Fbxw4)4Fsp/+,Fgf8tm1.4Mrt/Fgf8+
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv

 MP:0003494 parathyroid hypoplasia 
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0003606 kidney failure "cessation of renal function" [ncbi:Matthew Mailman, NCBI request]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(T-cre)1Lwd/0
Genetic Background: involves: 129P2/OlaHsd * C3H * C57BL/6 * CD-1

 MP:0003649 reduced right ventricle 
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Allelic Composition: Fgf8tm2Moon/Fgf8tm1Mrc,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10+,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

 MP:0003825 abnormal pillar cell morphology "abnormalities of the supporting cells that form the inner and outer walls of the tunnel in the organ of Corti " [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.3Mrt,Foxg1tm1(cre)Skm/Foxg1+
Genetic Background: involves: 129P2/OlaHsd

 MP:0003854 abnormal forelimb stylopod morphology 
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Allelic Composition: Grm1tm1Stl/Grm1tm1Stl
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0003855 abnormal forelimb zeugopod morphology 
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Allelic Composition: Grm1tm1Stl/Grm1tm1Stl
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0003856 abnormal hindlimb stylopod morphology 
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Allelic Composition: Grm1tm1Stl/Grm1tm1Stl
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0003857 abnormal hindlimb zeugopod morphology 
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Allelic Composition: Grm1tm1Stl/Grm1tm1Stl
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0003872 absent right ventricle "missing the lower right chamber of the heart" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Nkx2-5tm1(cre)Rjs/Nkx2-5+
Genetic Background: involves: 129P2/OlaHsd * 129S7/SvEvBrd

 MP:0003873 branchial arch hypoplasia "reduced size of the transient structures of the embryo that develop into regions of the head, neck and ears, due to reduced cell number" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Nkx2-5tm1(cre)Rjs/Nkx2-5+
Genetic Background: involves: 129P2/OlaHsd * 129S7/SvEvBrd

 MP:0003877 abnormal serotonergic neuron morphology "malformation or absence of the neurons that secrete serotonin" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator, J:54240]
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Allelic Composition: En1tm7(cre/ESR1)Alj/0,Fgf8tm1.1Jyhl/Fgf8tm1.3Mrt
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac

Allelic Composition: En1tm7(cre/ESR1)Alj/0,Fgf8tm1.3Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac

 MP:0003886 abnormal embryonic epiblast morphology "anomaly in the development/organization of the tissue that gives rise to the ectoderm, endoderm and mesoderm of the embryo proper" [brs:Beverly Richards-Smith, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf4tm1.2Mrt/Fgf4tm1.3Mrt,Tg(Msx2-cre)5Rem/0
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.4Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

 MP:0003920 abnormal right ventricle morphology "structural anomaly of the right lower chamber of the heart " [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm2Moon/Fgf8tm1Mrc,Isl1tm1(cre)Sev/Isl1+
Genetic Background: involves: 129S/Sv

 MP:0003931 absent molars "missing the most posterior teeth located on either side of the jaw, and characterized by a large crown and broad chewing surface" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

 MP:0003935 abnormal craniofacial development "anomaly in the process of forming the face and/or cranium" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm1.1Mrt/Fgf8tm1.2Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.3Mrt,Tg(Nes-cre)1Atp/0
Genetic Background: involves: 129P2/OlaHsd * FVB/N

 MP:0003984 embryonic growth retardation "slow or limited development before birth" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Del(19Poll-Fbxw4)4Fsp/+,Fgf8tm1.4Mrt/Fgf8+
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv

 MP:0004044 aortic dissection "a pathologic process, characterized by splitting of the media layer of the aorta, which leads to formation of a dissecting aneurysm" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(Tbx1-cre)1Joe/0
Genetic Background: Not Specified

 MP:0004083 polysyndactyly "greater than 5 digits present on an autopod with interdigital webbing also present" [rbabiuk:Randall Babiuk, Mouse Genome Informatics Curator]
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Allelic Composition: cir/cir+,Tmiesr/Tmie+
Genetic Background: involves: C57BL/6J * C57BL/How * ICR

 MP:0004110 transposition of great arteries "cardiovascular malformation in which the aorta arises from the right ventricle while the pulmonary artery arises from the left ventricle" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(Tbx1-cre)1Joe/0
Genetic Background: Not Specified

Allelic Composition: Fgf8tm2Moon/Fgf8tm1Mrc,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Fgf8tm2Moon/Fgf8tm1Mrc,Tg(Mef2c-cre)2Blk/0
Genetic Background: Not Specified

 MP:0004111 abnormal coronary artery morphology "anomaly of any of the arteries that branch from the aorta to supply blood to the heart" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0004113 abnormal aortic arch morphology "structural anomoly of the portion of the descending aorta proceeding from the arch of the aorta and extending to the diaphragm " [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Fgf8tm1.4Mrt/Fgf8+,Tbx1tm1Bld/Tbx1+
Genetic Background: involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * ICR

Allelic Composition: Fgf8tm1.4Mrt/Fgf8+,Tbx1tm4(cre/Esr1*)Bld/Tbx1+
Genetic Background: involves: 129P2/OlaHsd * 129S7/SvEvBrd

Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tbx1tm4(cre/Esr1*)Bld/Tbx1+
Genetic Background: involves: 129P2/OlaHsd * 129S7/SvEvBrd

Allelic Composition: Fgf8tm1.3Mrt/Fgf8+,Tbx1tm4(cre/Esr1*)Bld/Tbx1+
Genetic Background: involves: 129P2/OlaHsd * 129S7/SvEvBrd

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10+,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

 MP:0004157 interrupted aortic arch "complete discontinuation/blockage between the ascending and descending aorta; includes Type A, interruption distal to the subclavian artery that is ipsilateral to the second carotid artery, and Type B, interruption between second carotid artery and ipsilateral subclavian artery" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1.4Mrt/Fgf8+,Tbx1tm1Bld/Tbx1+
Genetic Background: involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * ICR

Allelic Composition: Gbx2tm1.1Mrt/Gbx2tm1.1Mrt,Fgf8tm1.4Mrt/Fgf8+
Genetic Background: B6.129-Gbx2tm1.1Mrt Fgf8tm1.4Mrt

Allelic Composition: Fgf8tm1.3Mrt/Fgf8+,Six1tm1(cre,ALPP)Xli/Six1+
Genetic Background: involves: 129 * 129P2/OlaHsd * C57BL/6

 MP:0004158 right aortic arch "the aortic arch lies to the right of the trachea and esophagus; results from persistance of the entire right dorsal arch and involution of a segment of the left arch" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1.4Mrt/Fgf8+,Tbx1tm1Bld/Tbx1+
Genetic Background: involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * ICR

Allelic Composition: Gbx2tm1.1Mrt/Gbx2+,Fgf8tm1.4Mrt/Fgf8+
Genetic Background: B6.129-Gbx2tm1.1Mrt Fgf8tm1.4Mrt

Allelic Composition: Gbx2tm1.1Mrt/Gbx2tm1.1Mrt,Fgf8tm1.4Mrt/Fgf8+
Genetic Background: B6.129-Gbx2tm1.1Mrt Fgf8tm1.4Mrt

Allelic Composition: Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10+,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

 MP:0004160 retroesophageal right subclavian artery "the subclavian artery aberrantly originates from the aortic arch distal to the origin of the left subclavian artery, i.e., it is the last branch of the aortic arch" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Gbx2tm1.1Mrt/Gbx2+,Fgf8tm1.4Mrt/Fgf8+
Genetic Background: B6.129-Gbx2tm1.1Mrt Fgf8tm1.4Mrt

Allelic Composition: Gbx2tm1.1Mrt/Gbx2tm1.1Mrt,Fgf8tm1.4Mrt/Fgf8+
Genetic Background: B6.129-Gbx2tm1.1Mrt Fgf8tm1.4Mrt

 MP:0004161 cervical aortic arch "aortic arch is located above the level of the clavicle" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm1.4Mrt/Fgf8+,Tbx1tm1Bld/Tbx1+
Genetic Background: involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * ICR

Allelic Composition: Fgf8tm1.3Mrt/Fgf8+,Six1tm1(cre,ALPP)Xli/Six1+
Genetic Background: involves: 129 * 129P2/OlaHsd * C57BL/6

 MP:0004201 fetal growth retardation "slow or limited development during the fetal period (sensu Mus: from E14 through birth)" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm3Mrc
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0004312 absent pillar cells "absence of the supporting cells that form the inner and outer walls of the tunnel in the organ of Corti" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.3Mrt,Foxg1tm1(cre)Skm/Foxg1+
Genetic Background: involves: 129P2/OlaHsd

 MP:0004318 absent incus "absence of the middle of the three auditory ossicles" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.3Mrt,Tg(Nes-cre)1Atp/0
Genetic Background: involves: 129P2/OlaHsd * FVB/N

 MP:0004439 absent Meckel s cartilage "absence of this cartilage bar in the mandibular arch that forms a temporary supporting structure in the embryonic mandible; gives rise to middle ear bones and sphenomandibular and anterior malleolar ligaments" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.3Mrt,Tg(Nes-cre)1Atp/0
Genetic Background: involves: 129P2/OlaHsd * FVB/N

 MP:0004575 small limb buds "reduced size of the mesenchymal outgrowth on the lateral trunk of the embryo that develops into the limbs" [MESH:National Library of Medicine_Medical Subject Headings]
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Allelic Composition: Grm1tm1Stl/Grm1tm1Stl
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0004592 small mandible "reduced size of the lower bony framework of the mouth where the inferior teeth are held" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Gbx2tm1.1Mrt/Gbx2tm1.1Mrt,Fgf8tm1.4Mrt/Fgf8+
Genetic Background: B6.129-Gbx2tm1.1Mrt Fgf8tm1.4Mrt

 MP:0004759 decreased mitotic index "decreased number of cells in G2/M phase" [Bertram_Weiss:Bayer_Schering_Pharma_AG]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm2Mrt,Nkx2-5tm1(cre)Rjs/Nkx2-5+
Genetic Background: involves: 129 * 129S7/SvEvBrd

 MP:0004837 abnormal neural fold formation "any anomaly in the process by which the edges of the neural plate thicken and move up to form a U-shaped structure called the neural groove" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf8tm1Jyhl/Fgf8tm1Jyhl
Genetic Background: involves: CD-1

 MP:0004861 abnormal Raphe nucleus morphology "any structural anomaly of the subgroup of the reticular nuclei of the brain stem that are located in and along the median plane of the medulla oblongata, pons, and mesencephalon that include neurons that synthesize serotonin and extend ascending fibers to parts of the limbic system and descending fibers to other brain stem nuclei, the medulla oblongata, and the pons" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: En1tm7(cre/ESR1)Alj/0,Fgf8tm1.1Jyhl/Fgf8tm1.3Mrt
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac

Allelic Composition: En1tm7(cre/ESR1)Alj/0,Fgf8tm1.3Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac

 MP:0004936 abnormal ureteric bud branching morphogenesis "partial or complete failure of the ureteric bud to repeatedly divide into lobules during development of the kidney" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(T-cre)1Lwd/0
Genetic Background: involves: 129P2/OlaHsd * C3H * C57BL/6 * CD-1

 MP:0005029 abnormal amnion "malformed innermost layer of the extraembryonic membranes" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, dlb:Donna Burkart , Mouse Genome Informatics Curator]
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Allelic Composition: Fgf4tm1.2Mrt/Fgf4tm1.3Mrt,Tg(Msx2-cre)5Rem/0
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.4Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.1Jyhl/Fgf8tm1.1Jyhl
Genetic Background: involves: CD-1

 MP:0005221 abnormal rostral-caudal axis patterning "anomaly in the development or formation of the axis that runs from the head to the tail of the body" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Fgf8tm1.1Mrt/Fgf8tm1.2Mrt
Genetic Background: involves: 129P2/OlaHsd

 MP:0005312 pericardial effusion "escape of fluid from blood vessels or lymphatics into the fibrous sac surrounding the heart" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Fgf8tm2Moon/Fgf8tm1Mrc,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6 * CBA

 MP:0005592 abnormal vascular smooth muscle morphology "structural anomaly of the nonstriated, involuntary muscle tissue of the blood vessels" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(Tbx1-cre)1Joe/0
Genetic Background: Not Specified

 MP:0005650 abnormal limb bud morphology "aberrant structure or development of any of the swellings on the trunk of the embryo that become limbs" [hdene:Howard Dene , Mouse Genome Informatics Curator, MeSH:National Library of Medicine - Medical Subject Headings , 2003, J:61460]
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Allelic Composition: cir/cir+,Tmiesr/Tmie+
Genetic Background: involves: C57BL/6J * C57BL/How * ICR

 MP:0006032 abnormal ureteric bud morphology "anomaly in the formation or development of the ureteric bud that with the metanephric mesenchyme gives rise to the kidneys " [smb:Susan M Bello, Mouse Genome Informatics Curator, J:57313:]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(T-cre)1Lwd/0
Genetic Background: involves: 129P2/OlaHsd * C3H * C57BL/6 * CD-1

 MP:0006042 increased apoptosis "greater than normal programmed cell death" [RGD:Rat Genome Database submission, smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm2Moon/Fgf8tm1Mrc,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Fgf8tm2Moon/Fgf8tm1Mrc,Isl1tm1(cre)Sev/Isl1+
Genetic Background: involves: 129S/Sv

 MP:0006126 abnormal outflow tract development "anomaly in the development of the common arterial trunk that forms the aorta and pulmonary artery" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf8tm2Moon/Fgf8tm1Mrc,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Moon,Isl1tm1(cre)Sev/Isl1+
Genetic Background: involves: 129S/Sv * Black Swiss * C57BL/6

Allelic Composition: Fgf8tm1.3Mrt/Fgf8+,Six1tm1(cre,ALPP)Xli/Six1+
Genetic Background: involves: 129 * 129P2/OlaHsd * C57BL/6

Allelic Composition: Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10+,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

 MP:0006279 abnormal limb development "anomaly in the formation of the limbs" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Grm1tm1Stl/Grm1tm1Stl
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(CAG-Bgeo,-Fgf4)1Mrt/?,Tg(Msx2-cre)5Rem/?
Genetic Background: involves: 129P2/OlaHsd

 MP:0006280 abnormal digit development "anomaly in the formation of the digits" [J:70592, MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Grm1tm1Stl/Grm1tm1Stl
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(CAG-Bgeo,-Fgf4)1Mrt/?,Tg(Msx2-cre)5Rem/?
Genetic Background: involves: 129P2/OlaHsd

 MP:0006306 abnormal nasal pit morphology "malformation of one or both of a pair of depressions formed in the developing face that give rise to the rostral portion of the nasal meatus" [J:119812, MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf8tm1.4Mrt/Fgf8+,Tfap2atm1Will/Tfap2atm2.1Will
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * Black Swiss

 MP:0006325 impaired hearing "reduced ability to percieve auditory stimuli" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Ripk2tm1Flv/Ripk2tm1Flv
Genetic Background: involves: 129S1/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8+,Fgf9tm1Dor/Fgf9+,Fgfr3tm1.1Aomw/Fgfr3+
Genetic Background: involves: 129 * BALB/c * C57BL/6

 MP:0006331 abnormal patterning of the organ of Corti "anomaly in the organization of the various cell types within the organ of Corti into a set number of distinct rows" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.3Mrt,Foxg1tm1(cre)Skm/Foxg1+
Genetic Background: involves: 129P2/OlaHsd

 MP:0006341 small first branchial arch "reduced size of the first branchial arch" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.3Mrt,Tg(Nes-cre)1Atp/0
Genetic Background: involves: 129P2/OlaHsd * FVB/N

 MP:0006346 small branchial arch "reduced size of one or more of the branchial arches" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf8tm2Moon/Fgf8tm1Mrc,Isl1tm1(cre)Sev/Isl1+
Genetic Background: involves: 129S/Sv

 MP:0006354 abnormal fourth branchial arch artery morphology "any structural anomaly of the vessels formed within the fourth pair of branchial arches in embryogenesis" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1.4Mrt/Fgf8+,Tbx1tm1Bld/Tbx1+
Genetic Background: involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * ICR

Allelic Composition: Chd7Gt(XK403)Byg/Chd7+,Fgf8tm1.2Mrt/Fgf8+
Genetic Background: either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * CD-1)

Allelic Composition: Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10+,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

 MP:0006355 abnormal sixth branchial arch artery morphology "any structural anomaly of the vessels formed within the sixth pair of branchial arches in embryogenesis" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10+,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

 MP:0006356 abnormal third branchial arch artery morphology "any structural anomaly of the vessels formed within the third pair of branchial arches in embryogenesis" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10+,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

 MP:0006386 absent somites "missing all somites" [MGI:rbabiuk "Randall Babiuk, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf4tm1.2Mrt/Fgf4tm1.3Mrt,Tg(Msx2-cre)5Rem/0
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.4Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

 MP:0008825 abnormal cardiac epithelial to mesenchymal transition "anomaly in the process by which endocardial cells of the atrioventricular canal lose their epithelial characteristics, delaminante from the endocardial sheet, become migratory and invade the cardiac jelly, and develop mesenchymal characteristics eventaully forming the endocardial cushions reqired for septum and atrioventricular valve formation" [PMID:17303760]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Moon,Isl1tm1(cre)Sev/Isl1+
Genetic Background: involves: 129S/Sv * Black Swiss * C57BL/6

Allelic Composition: Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

 MP:0008919 fused tarsal bones "anomaly of the eight bones of the instep of the paw/foot resulting in some or all the bones being joined together" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(CAG-Bgeo,-Fgf4)1Mrt/?,Tg(Msx2-cre)5Rem/?
Genetic Background: involves: 129P2/OlaHsd

 MP:0009038 decreased inferior colliculus size "decreased size of the paired inferior eminence of the mesencephalic tectum" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf8tm1.4Mrt/Fgf8+,Fgf17tm1Dor/Fgf17tm1Dor
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac

Allelic Composition: Fgf17tm1Dor/Fgf17tm1Dor,Fgf8tm1.1Jyhl/Fgf8tm1.1Jyhl
Genetic Background: involves: 129S6/SvEvTac

 MP:0009039 absent inferior colliculus "absence of the paired inferior eminence of the mesencephalic tectum" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf4tm1.2Mrt/Fgf4tm1.3Mrt,Tg(Msx2-cre)5Rem/0
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.1Mrt/Fgf8tm1.2Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.4Mrt/Fgf8+,Gli3tm1.1Alj/Gli3tm1.1Alj
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6

 MP:0009048 enlarged tectum "increased size of the rostral part of the midbrain roof" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf8tm1.4Mrt/Fgf8+,Gli3tm1.1Alj/Gli3tm1.1Alj
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6

 MP:0009331 absent primitive node "absence of the regional thickening of cells at the rostral tip of the vertebrate primitive streak through which gastrulating cells migrate anteriorally to form tissues in the future head and neck; this region organizes the formation of the three embryonic layers and establishes the longitudinal axis and the polarity of the embryo" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf4tm1.2Mrt/Fgf4tm1.3Mrt,Tg(Msx2-cre)5Rem/0
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.4Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.1Jyhl/Fgf8tm1.1Jyhl
Genetic Background: involves: CD-1

 MP:0009844 abnormal neural crest cell apoptosis "change in the timing or the number of neural crest cells undergoing programmed cell death" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm3Mrc
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0009845 abnormal neural crest cell morphology "any structural anomaly of the transient and migratory group of cells that emerge from the dorsal region of the neural tube and disperse to many peripheral locations to form various tissues of the adult" [ISBN:0838580343 "Kandel ER, et al. Principles of Neural Science, 3rd edition", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm2Mrt,Nkx2-5tm1(cre)Rjs/Nkx2-5+
Genetic Background: involves: 129 * 129S7/SvEvBrd

 MP:0009893 cleft primary palate "congenital fissure of the tissues normally uniting to form the primary palate" [PMID:16680722]
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Allelic Composition: Fgf8tm1.4Mrt/Fgf8+,Tfap2atm1Will/Tfap2atm2.1Will
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * Black Swiss

 MP:0009907 decreased tongue size "reduced size of the mobile mass of muscular tissue and surrounding epithelial tissue occupying the cavity of the mouth and forming part of the floor" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.3Mrt,Tg(Nes-cre)1Atp/0
Genetic Background: involves: 129P2/OlaHsd * FVB/N

 MP:0010241 abnormal aortic arch development "anomaly in the process of forming the convex portion of the aorta between the ascending and descending parts of the aorta; including formation of the brachiocephalic trunk, the left common carotid artery, and the left subclavian artery; the brachiocephalic trunk further splits to form the right subclavian artery and the right common carotid artery" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Fgf8tm1.4Mrt/Fgf8+,Tbx1tm1Bld/Tbx1+
Genetic Background: involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * ICR

 MP:0010402 ventricular septal defect "abnormal communications between the two lower chambers of the heart, including such defects in the perimembranous, inlet, outlet (infundibular), central muscular, marginal muscular, or apical muscular regions" [MESH:C14.240.400.560.540]
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Allelic Composition: Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10+,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

 MP:0010403 atrial septal defect "abnormal communications between the two upper chambers of the heart, including such defects in any or all of the ostium primum, ostium secundum, sinus venosus, and coronary sinus regions" [MESH:C14.240.400.560.375]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(Tbx1-cre)1Joe/0
Genetic Background: Not Specified

 MP:0010406 absent atrial septum "absence of the thin membranous structure between the two heart atria" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf8tm2Moon/Fgf8tm1Mrc,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6 * CBA

 MP:0010418 perimembraneous ventricular septal defect "abnormal communications between the two lower chambers of the heart, occurring in the membranous septum with defects in the adjacent muscular portion of the septum; it is generally located in the LV outflow tract just below the aortic valve, associated with pouches or aneurysms of the septal leaflet of the tricuspid valve, which may partially or completely close the defect; an LV-to-RA shunt may also be associated with this defect" [http://emedicine.medscape.com]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(Tbx1-cre)1Joe/0
Genetic Background: Not Specified

 MP:0010432 common ventricle "the presence of only one working lower chamber in the heart, usually with a virtual absence of the ventricular septum and usually present in conjunction with double inlet left or right ventricle" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf8tm2Moon/Fgf8tm1Mrc,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6 * CBA

 MP:0010454 abnormal truncus arteriosis septation "anomaly in the process of dividing the common arterial trunk arising out of both heart ventricles to divide into the aorta and pulmonary artery during development" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm2Moon/Fgf8tm1Mrc,Isl1tm1(cre)Sev/Isl1+
Genetic Background: involves: 129S/Sv

Allelic Composition: Fgf8tm1Mrc/Fgf8tm3Mrc
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0010465 aberrant origin of the right subclavian artery "the right subclavian artery arises from an atypical location on the aortic arch or the proximal descending aorta" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10+,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

 MP:0010484 bicuspid aortic valve "the presence of two cusps in the aortic valve instead of three" [http://emedicine.medscape.com]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm2Moon/Fgf8tm1Mrc,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6 * CBA

 MP:0010527 bicuspid pulmonary valve "the presence of two cusps or leaflets in the pulmonary valve instead of three" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf8tm2Moon/Fgf8tm1Mrc,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6 * CBA

 MP:0010551 abnormal coronary vessel morphology "any structural anomaly of any of the arteries or veins that supply blood to the heart or return blood from the heart muscles to the circulation" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0010585 abnormal conotruncal ridge morphology "any structural anomaly of the pair of spiral mesenchymal swellings in the primordial ventricular outflow tract, that eventually fuse to form the conotruncal septum, dividing the subvalvular outflow tract and contributing to the membranous interventricular septum" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", PMID:8823298]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Moon,Isl1tm1(cre)Sev/Isl1+
Genetic Background: involves: 129S/Sv * Black Swiss * C57BL/6

 MP:0011085 complete postnatal lethality "premature death anytime between the neonatal period and weaning age of all organisms of a given genotype in a population (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0011086 partial postnatal lethality "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms anytime between the neonatal period and weaning age (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith]
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Allelic Composition: Fgf8tm2.1Jyhl/Fgf8+
Genetic Background: B6.129S6-Fgf8tm2.1Jyhl

 MP:0011087 complete neonatal lethality "death of all organisms of a given genotype in a population within the neonatal period after birth (Mus: P0)" [MGI:csmith]
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Allelic Composition: Fgf4tm1.2Mrt/Fgf4tm1.3Mrt,Tg(Msx2-cre)5Rem/0
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.3Mrt,Tg(Nes-cre)1Atp/0
Genetic Background: involves: 129P2/OlaHsd * FVB/N

Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(T-cre)1Lwd/0
Genetic Background: involves: 129P2/OlaHsd * C3H * C57BL/6 * CD-1

Allelic Composition: Fgf8tm1Mrc/Fgf8tm3Mrc
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0011088 partial neonatal lethality "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms within the neonatal period after birth (Mus: P0)" [MGI:csmith]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0011089 complete perinatal lethality "death of all organisms of a given genotype in a population within the perinatal period (Mus: E18.5 through postnatal day 1)" [MGI:csmith]
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Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.3Mrt,Foxg1tm1(cre)Skm/Foxg1+
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: En1tm7(cre/ESR1)Alj/0,Fgf8tm1.1Jyhl/Fgf8tm1.3Mrt
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac

 MP:0011090 partial perinatal lethality "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms within the perinatal period (Mus: E18.5 through postnatal day 1)" [MGI:csmith]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(Tbx1-cre)1Joe/0
Genetic Background: Not Specified

 MP:0011098 complete embryonic lethality during organogenesis "death of all organisms of a given genotype in a population between embryo turning and the completion of organogenesis (Mus: E9 to less than E14)" [MGI:csmith]
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Allelic Composition: Fgf4tm1.2Mrt/Fgf4tm1.3Mrt,Tg(Msx2-cre)5Rem/0
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.4Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Nkx2-5tm1(cre)Rjs/Nkx2-5+
Genetic Background: involves: 129P2/OlaHsd * 129S7/SvEvBrd

 MP:0011100 complete preweaning lethality "death of all organisms of a given genotype in a population between fertilization and weaning age (Mus: approximately 3-4 weeks of age)" [MGI:csmith]
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Allelic Composition: Fgf10tm1b(EUCOMM)Wtsi/Fgf10+
Genetic Background: C57BL/6N-Fgf10tm1b(EUCOMM)Wtsi/H

 MP:0011101 partial prenatal lethality "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms between fertilization and birth (Mus: approximately E18.5)" [MGI:csmith]
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Allelic Composition: Fgf8tm1.1Mrt/Fgf8tm1.2Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Del(19Poll-Fbxw4)4Fsp/+,Fgf8tm1.4Mrt/Fgf8+
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv

 MP:0011108 partial embryonic lethality during organogenesis "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms between embryo turning and the completion of organogenesis (Mus: E9 to less than E14)" [MGI:csmith]
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Allelic Composition: Fgf8tm2Moon/Fgf8tm1Mrc,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Fgf8tm2Moon/Fgf8tm1Mrc,Isl1tm1(cre)Sev/Isl1+
Genetic Background: involves: 129S/Sv

 MP:0011262 abnormal branchial arch mesenchyme morphology "any structural anomaly in the primordial embryonic connective tissue associated with the branchial arches, consisting of mesenchymal cells supported in interlaminar jelly, that derive mostly from the mesoderm and contribute to facial and cranial nerve-associated structures" [ISBN:0-683-40008-8, MGI:csmith]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm2Mrt,Nkx2-5tm1(cre)Rjs/Nkx2-5+
Genetic Background: involves: 129 * 129S7/SvEvBrd

 MP:0011354 absent renal glomerulus "complete absence of the tuft formed of capillary loops and mesangium at the beginning of each nephretic tubule in the kidney that normally function as a filtration unit" [ISBN:0-683-40008-8]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(T-cre)1Lwd/0
Genetic Background: involves: 129P2/OlaHsd * C3H * C57BL/6 * CD-1

 MP:0011368 increased kidney apoptosis "increase in the number of cells of the kidney undergoing programmed cell death" [MGI:anna]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(T-cre)1Lwd/0
Genetic Background: involves: 129P2/OlaHsd * C3H * C57BL/6 * CD-1

 MP:0011388 absent heart "absence of the hollow, muscular organ that maintains the circulation of the blood" [MGI:smb]
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Allelic Composition: Fgf4tm1.2Mrt/Fgf4tm1.3Mrt,Tg(Msx2-cre)5Rem/0
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.4Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

 MP:0011448 decreased dopaminergic neuron number "fewer than normal numbers of the neurons that utilize dopamine as a neurotransmitter" [MGI:smb]
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Allelic Composition: En1tm7(cre/ESR1)Alj/0,Fgf8tm1.1Jyhl/Fgf8tm1.3Mrt
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac

Allelic Composition: En1tm7(cre/ESR1)Alj/0,Fgf8tm1.3Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac

 MP:0011967 increased or absent threshold for auditory brainstem response "increase in the value at which one or more sound frequencies or broadband clicks first elicits a recordable response generated by electrical activity of neurons in the ascending auditory system, or complete lack of a recordable response at any frequency or broadband click" [MGI:csmith]
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Allelic Composition: Fgf8tm1Mrc/Fgf8+,Fgfr3tm1.1Aomw/Fgfr3+
Genetic Background: involves: 129 * BALB/c * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8+,Fgf9tm1Dor/Fgf9+,Fgfr3tm1.1Aomw/Fgfr3+
Genetic Background: involves: 129 * BALB/c * C57BL/6

 MP:0012179 abnormal splanchnic mesoderm morphology "any structural abnormality of the inner layer of lateral plate mesoderm, located above (dorsally) the endoderm, which forms the circulatory system and future gut wall" [MGI:anna]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm2Mrt,Nkx2-5tm1(cre)Rjs/Nkx2-5+
Genetic Background: involves: 129 * 129S7/SvEvBrd

Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sortm1Sor,Nkx2-5tm1(cre)Rjs/Nkx2-5+
Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJaeSor * 129S7/SvEvBrd

 MP:0012278 abnormal cardiogenic mesoderm morphology "any structural anomaly of the splanchnic mesoderm in the cardiogenic region where the heart develops; it gives rise to endocardial heart tubes that fuse to form the primordial cardiac tube, the heart primordium" [MGI:anna]
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Allelic Composition: Fgf8tm1Jyhl/Fgf8tm1Jyhl
Genetic Background: involves: CD-1

 MP:0012685 abnormal primitive streak elongation "any anomaly in the process by which the primitive streak extends anteriorly and elongates towards the distal (cranial) end of the embryo to reach its full length" [MGI:anna]
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Allelic Composition: Fgf4tm1.2Mrt/Fgf4tm1.3Mrt,Tg(Msx2-cre)5Rem/0
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.4Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Fgf8tm1.2Mrt/Fgf8tm1.4Mrt
Genetic Background: involves: 129P2/OlaHsd

 MP:0012729 abnormal common carotid artery morphology "any structural anomaly of the left or right common carotid arteries which extend headward on each side of the anterior neck and deliver oxygenated nutrient filled blood from the heart to the head, neck and brain; the left originates in the arch of the aorta over the heart; the right originates in the brachiocephalic trunk, the largest branch from the arch of the aorta; each common carotid artery divides into an external and an internal carotid artery" [MGI:anna]
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Allelic Composition: Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10+,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

 MP:0012730 abnormal internal carotid artery morphology "any structural anomaly of the terminal branch of the left or right common carotid artery which supplies oxygenated blood to the brain and eyes" [MGI:anna]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Tg(Tbx1-cre)1Joe/0
Genetic Background: Not Specified

 MP:0012752 abnormal cardiac neural crest cell migration "any anomaly in the migratory path of cardiac neural crest cells (NCCs), a subpopulation of cranial NCCs which originate from the lower hindbrain between the otic placode and third somite and migrate to the circumpharyngeal ridge (an arc-shape ridge located dorsal to the forming caudal pharyngeal arches) and then into the 3rd, 4th and 6th pharyngeal arches and the cardiac outflow tract (OFT); cardiac NCCs undergo migration away from the neural tube by following a dorsolateral path under the ectoderm, leading them to the pharyngeal arches; after pausing, they resume migration under the pharyngeal endoderm and, along the aortic arch arteries, populate the cardiac OFT where they contribute the aorticopulmonary septum, and ultimately colonize the heart to form the ventricular septum and cardiac ganglia" [MGI:anna]
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Allelic Composition: Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

 MP:0013268 second pharyngeal arch hypoplasia "underdevelopment or reduced size of the second pharyngeal arch, usually due to reduced cell number" [MGI:anna]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10+,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

 MP:0013269 third pharyngeal arch hypoplasia "underdevelopment or reduced size of the third pharyngeal arch, usually due to reduced cell number" [MGI:anna]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

Allelic Composition: Fgf10tm1Ska/Fgf10+,Fgf8tm1Moon/Fgf8tm1Moon,Mesp1tm2(cre)Ysa/Mesp1+
Genetic Background: involves: C57BL/6NCrlj * CBA/JNCrlj

 MP:0013293 embryonic lethality prior to tooth bud stage "death prior to the appearance of tooth buds (Mus: E12-E12.5)" [MGI:smb]
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Allelic Composition: Fgf10tm1b(EUCOMM)Wtsi/Fgf10+
Genetic Background: C57BL/6N-Fgf10tm1b(EUCOMM)Wtsi/H

 MP:0013574 ectopic parathyroid gland "a parathyroid gland located outside of its normal position; in the normal adult mouse, the parathyroids are usually found embedded in the connective tissue capsule on the posterior surface of the thyroid gland; because of their common pharyngeal pouch origin, ectopic thyroid and parathyroid tissue can occasionally be found in the thymus" [MGI:Anna]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0014044 absent cardiac outflow tract "absence of or complete failure to form the common arterial trunk that normally forms the aorta and pulmonary artery and the ventricular outflow regions" [MGI:anna]
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Allelic Composition: Fgf8tm1.3Mrt/Fgf8tm1.4Mrt,Nkx2-5tm1(cre)Rjs/Nkx2-5+
Genetic Background: involves: 129P2/OlaHsd * 129S7/SvEvBrd

 MP:0030095 abnormal midface morphology "any structural anomaly of the midface region which extends, superiorly, from the inferior orbital margin to, inferiorly, the level of nasal base; it is formed by the maxilla (upper jaw) and zygoma and cheeks and malar region; traditionally, the nose and premaxilla are not included in the midface" [HP:0000309, PMID:19125436]
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Allelic Composition: Fgf8tm1.4Mrt/Fgf8+,Tfap2atm1Will/Tfap2atm2.1Will
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * Black Swiss

 MP:0030334 absent sixth pharyngeal arch artery "failure to develop or absence of the sixth pharyngeal arch artery" [MGI:anna]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0030336 third pharyngeal arch artery hypoplasia "underdevelopment or reduced size of the third pharyngeal arch artery, usually due to a reduced number of cells" [MGI:anna]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm3Mrc
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0030337 enlarged third pharyngeal arch artery "increased size of the third pharyngeal arch artery" [MGI:anna]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Hoxa3tm1(cre)Moon/Hoxa3+
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0030340 absent fourth pharyngeal arch artery "failure to develop or absence of the fourth pharyngeal arch artery" [MGI:anna]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0030341 fourth pharyngeal arch artery hypoplasia "underdevelopment or reduced size of the fourth pharyngeal arch artery, usually due to a reduced number of cells" [MGI:anna]
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Allelic Composition: Fgf8tm1Mrc/Fgf8tm2Mrc,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Fgf8tm1Mrc/Fgf8tm1Moon,Tfap2atm1(cre)Moon/Tfap2a+
Genetic Background: involves: 129/Sv * C57BL/6

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

1 s.

 
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