ENSMUSG00000021732


Mus musculus

Features
Gene ID: ENSMUSG00000021732
  
Biological name :Fgf10
  
Synonyms : Fgf10 / Fibroblast growth factor 10 / O35565
  
Possible biological names infered from orthology : O15520
  
Species: Mus musculus
  
Chr. number: 13
Strand: 1
Band: D2.3
Gene start: 118669791
Gene end: 118792115
  
Corresponding Affymetrix probe sets: 10407350 (MoGene1.0st)   1420690_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000022246
NCBI entrez gene - 14165     See in Manteia.
MGI - MGI:1099809
RefSeq - NM_008002
RefSeq Peptide - NP_032028
swissprot - O35565
Ensembl - ENSMUSG00000021732
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 fgf10aENSDARG00000030932Danio rerio
 fgf10bENSDARG00000100475Danio rerio
 FGF10ENSGALG00000014872Gallus gallus
 FGF10ENSG00000070193Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Fgf7 / P36363 / Fibroblast growth factor 7 / P21781*ENSMUSG0000002720845
Fgf3 / fibroblast growth factor 3 / P11487*ENSMUSG0000003107438
Fgf22 / Q9ESS2 / Fibroblast growth factor 22 / Q9HCT0*ENSMUSG0000002032737
Fgf5 / P15656 / Fibroblast growth factor 5 / P12034*ENSMUSG0000002933730
Fgf6 / P21658 / Fibroblast growth factor 6 / P10767*ENSMUSG0000000018330
Fgf20 / Q9ESL9 / Fibroblast growth factor 20 / Q9NP95*ENSMUSG0000003160330
Fgf16 / Q9ESL8 / Fibroblast growth factor 16 / O43320*ENSMUSG0000003123029
Fgf9 / P54130 / Fibroblast growth factor 9 / P31371*ENSMUSG0000002197429
Fgf13 / P70377 / Mus musculus fibroblast growth factor 13 (Fgf13), transcript variant 4, mRNA. / Q92913* / fibroblast growth factor 13*ENSMUSG0000003113726
Fgf12 / P61329 / Fibroblast growth factor 12 / P61328*ENSMUSG0000002252325
Fgf4 / P11403 / Fibroblast growth factor 4 / P08620*ENSMUSG0000005091724
Fgf11 / P70378 / Fibroblast growth factor 11 / Q92914*ENSMUSG0000004282622
Fgf14 / fibroblast growth factor 14 / Q92915*ENSMUSG0000002555121


Protein motifs (from Interpro)
Interpro ID Name
 IPR002209  Fibroblast growth factor family
 IPR008996  Cytokine IL1/FGF
 IPR028252  Fibroblast growth factor 10


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0000132 establishment of mitotic spindle orientation IGI
 biological_processGO:0000187 activation of MAPK activity IEA
 biological_processGO:0001525 angiogenesis IEA
 biological_processGO:0001656 metanephros development IEA
 biological_processGO:0001759 organ induction IEA
 biological_processGO:0001823 mesonephros development IEA
 biological_processGO:0001974 blood vessel remodeling IGI
 biological_processGO:0003338 metanephros morphogenesis IMP
 biological_processGO:0006935 chemotaxis IDA
 biological_processGO:0007267 cell-cell signaling IMP
 biological_processGO:0007368 determination of left/right symmetry IMP
 biological_processGO:0007431 salivary gland development IEA
 biological_processGO:0007435 salivary gland morphogenesis IMP
 biological_processGO:0008284 positive regulation of cell proliferation IDA
 biological_processGO:0008285 negative regulation of cell proliferation IDA
 biological_processGO:0008543 fibroblast growth factor receptor signaling pathway IEA
 biological_processGO:0008544 epidermis development IMP
 biological_processGO:0008589 regulation of smoothened signaling pathway IMP
 biological_processGO:0009880 embryonic pattern specification IMP
 biological_processGO:0009887 animal organ morphogenesis IMP
 biological_processGO:0010468 regulation of gene expression IMP
 biological_processGO:0010469 regulation of signaling receptor activity IEA
 biological_processGO:0010631 epithelial cell migration IMP
 biological_processGO:0010634 positive regulation of epithelial cell migration IEA
 biological_processGO:0010838 positive regulation of keratinocyte proliferation IEA
 biological_processGO:0014070 response to organic cyclic compound IEA
 biological_processGO:0021983 pituitary gland development IMP
 biological_processGO:0030154 cell differentiation IEA
 biological_processGO:0030177 positive regulation of Wnt signaling pathway IMP
 biological_processGO:0030324 lung development IMP
 biological_processGO:0030538 embryonic genitalia morphogenesis IMP
 biological_processGO:0030855 epithelial cell differentiation IMP
 biological_processGO:0030878 thyroid gland development IMP
 biological_processGO:0030916 otic vesicle formation TAS
 biological_processGO:0030949 positive regulation of vascular endothelial growth factor receptor signaling pathway IMP
 biological_processGO:0031016 pancreas development IMP
 biological_processGO:0031069 hair follicle morphogenesis IMP
 biological_processGO:0031076 embryonic camera-type eye development IMP
 biological_processGO:0031532 actin cytoskeleton reorganization IEA
 biological_processGO:0031659 positive regulation of cyclin-dependent protein serine/threonine kinase activity involved in G1/S transition of mitotic cell cycle IEA
 biological_processGO:0032355 response to estradiol IEA
 biological_processGO:0032496 response to lipopolysaccharide IEA
 biological_processGO:0032781 positive regulation of ATPase activity IEA
 biological_processGO:0032808 lacrimal gland development IEA
 biological_processGO:0032925 regulation of activin receptor signaling pathway IMP
 biological_processGO:0034394 protein localization to cell surface IEA
 biological_processGO:0035019 somatic stem cell population maintenance IMP
 biological_processGO:0035108 limb morphogenesis IMP
 biological_processGO:0035265 organ growth IMP
 biological_processGO:0042060 wound healing IEA
 biological_processGO:0042246 tissue regeneration IEA
 biological_processGO:0042472 inner ear morphogenesis IMP
 biological_processGO:0042475 odontogenesis of dentin-containing tooth IMP
 biological_processGO:0042693 muscle cell fate commitment IMP
 biological_processGO:0043410 positive regulation of MAPK cascade IEA
 biological_processGO:0043616 keratinocyte proliferation IMP
 biological_processGO:0045596 negative regulation of cell differentiation IDA
 biological_processGO:0045739 positive regulation of DNA repair IEA
 biological_processGO:0045740 positive regulation of DNA replication IEA
 biological_processGO:0045747 positive regulation of Notch signaling pathway IGI
 biological_processGO:0045893 positive regulation of transcription, DNA-templated IDA
 biological_processGO:0045931 positive regulation of mitotic cell cycle IMP
 biological_processGO:0045944 positive regulation of transcription by RNA polymerase II IDA
 biological_processGO:0046579 positive regulation of Ras protein signal transduction IEA
 biological_processGO:0046877 regulation of saliva secretion IEA
 biological_processGO:0048146 positive regulation of fibroblast proliferation IMP
 biological_processGO:0048286 lung alveolus development IMP
 biological_processGO:0048514 blood vessel morphogenesis IMP
 biological_processGO:0048536 spleen development IMP
 biological_processGO:0048538 thymus development IEA
 biological_processGO:0048557 embryonic digestive tract morphogenesis IMP
 biological_processGO:0048565 digestive tract development IMP
 biological_processGO:0048566 embryonic digestive tract development IMP
 biological_processGO:0048645 animal organ formation IMP
 biological_processGO:0048730 epidermis morphogenesis IMP
 biological_processGO:0048752 semicircular canal morphogenesis IGI
 biological_processGO:0048754 branching morphogenesis of an epithelial tube IEA
 biological_processGO:0048807 female genitalia morphogenesis IMP
 biological_processGO:0048808 male genitalia morphogenesis IMP
 biological_processGO:0050671 positive regulation of lymphocyte proliferation IEA
 biological_processGO:0050673 epithelial cell proliferation IEA
 biological_processGO:0050674 urothelial cell proliferation IEA
 biological_processGO:0050677 positive regulation of urothelial cell proliferation IEA
 biological_processGO:0050678 regulation of epithelial cell proliferation IMP
 biological_processGO:0050679 positive regulation of epithelial cell proliferation IEA
 biological_processGO:0050731 positive regulation of peptidyl-tyrosine phosphorylation IEA
 biological_processGO:0050872 white fat cell differentiation IMP
 biological_processGO:0050918 positive chemotaxis IEA
 biological_processGO:0050930 induction of positive chemotaxis IDA
 biological_processGO:0051145 smooth muscle cell differentiation IMP
 biological_processGO:0051549 positive regulation of keratinocyte migration IEA
 biological_processGO:0060019 radial glial cell differentiation IMP
 biological_processGO:0060173 limb development IMP
 biological_processGO:0060174 limb bud formation IMP
 biological_processGO:0060425 lung morphogenesis IMP
 biological_processGO:0060428 lung epithelium development IEA
 biological_processGO:0060430 lung saccule development IEA
 biological_processGO:0060436 bronchiole morphogenesis IMP
 biological_processGO:0060441 epithelial tube branching involved in lung morphogenesis IMP
 biological_processGO:0060445 branching involved in salivary gland morphogenesis IGI
 biological_processGO:0060447 bud outgrowth involved in lung branching IEA
 biological_processGO:0060449 bud elongation involved in lung branching IGI
 biological_processGO:0060496 mesenchymal-epithelial cell signaling involved in lung development IDA
 biological_processGO:0060510 type II pneumocyte differentiation IDA
 biological_processGO:0060513 prostatic bud formation IGI
 biological_processGO:0060541 respiratory system development IDA
 biological_processGO:0060594 mammary gland specification IGI
 biological_processGO:0060595 fibroblast growth factor receptor signaling pathway involved in mammary gland specification IEA
 biological_processGO:0060615 mammary gland bud formation IMP
 biological_processGO:0060661 submandibular salivary gland formation IMP
 biological_processGO:0060664 epithelial cell proliferation involved in salivary gland morphogenesis IMP
 biological_processGO:0060665 regulation of branching involved in salivary gland morphogenesis by mesenchymal-epithelial signaling IDA
 biological_processGO:0060667 branch elongation involved in salivary gland morphogenesis IMP
 biological_processGO:0060879 semicircular canal fusion IMP
 biological_processGO:0060915 mesenchymal cell differentiation involved in lung development IGI
 biological_processGO:0061033 secretion by lung epithelial cell involved in lung growth IEA
 biological_processGO:0061115 lung proximal/distal axis specification IDA
 biological_processGO:0070075 tear secretion IEA
 biological_processGO:0070352 positive regulation of white fat cell proliferation IMP
 biological_processGO:0070371 ERK1 and ERK2 cascade IEA
 biological_processGO:0070374 positive regulation of ERK1 and ERK2 cascade IEA
 biological_processGO:0070384 Harderian gland development IMP
 biological_processGO:0071157 negative regulation of cell cycle arrest IEA
 biological_processGO:0071338 positive regulation of hair follicle cell proliferation IEA
 biological_processGO:0090263 positive regulation of canonical Wnt signaling pathway IMP
 biological_processGO:2001240 negative regulation of extrinsic apoptotic signaling pathway in absence of ligand IMP
 cellular_componentGO:0005576 extracellular region IEA
 cellular_componentGO:0005615 extracellular space IEA
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005886 plasma membrane IEA
 cellular_componentGO:0009986 cell surface IEA
 cellular_componentGO:0031012 extracellular matrix IEA
 molecular_functionGO:0005104 fibroblast growth factor receptor binding ISO
 molecular_functionGO:0005111 type 2 fibroblast growth factor receptor binding IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0008083 growth factor activity ISO
 molecular_functionGO:0008201 heparin binding IEA
 molecular_functionGO:0042056 chemoattractant activity IEA


Pathways (from Reactome)
Pathway description
PI3K Cascade
PIP3 activates AKT signaling
FGFR1b ligand binding and activation
FGFR2b ligand binding and activation
Phospholipase C-mediated cascade: FGFR1
Phospholipase C-mediated cascade; FGFR2
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
FRS-mediated FGFR3 signaling
FRS-mediated FGFR4 signaling
Negative regulation of FGFR1 signaling
Negative regulation of FGFR2 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:0000003 abnormal adipose tissue morphology "structural anomaly of the connective tissue composed of fat cells enmeshed in areolar tissue" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Fbxw4Dac/Fbxw4Dac,mdac/mdac
Genetic Background: involves: SM/Ckc

 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: Cd19tm1(cre)Cgn/Cd19+,Ube2ntm1Aki/Ube2ntm1Aki
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0000026 abnormal inner ear morphology "malformation or malfunction of any components of the labyrinth, including the semicircular canals, vestibule and cochlea" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:1776]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0000031 abnormal cochlea morphology "any anomaly, deformity, malformation, impairment or dysfunction of the cochlea" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, cml:Cathleen M. Lutz , Mouse Genome Informatics Curator, J:21484]
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Allelic Composition: Cd19tm1(cre)Cgn/Cd19+,Ube2ntm1Aki/Ube2ntm1Aki
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0000034 abnormal vestibule morphology "malformed cavity between the semicircular canals and the cochlea of the inner ear" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:1776]
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Allelic Composition: Cd19tm1(cre)Cgn/Cd19+,Ube2ntm1Aki/Ube2ntm1Aki
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0000149 abnormal scapula morphology "malformation of either or both of the large, flat bones of the back part of the shoulder" [J:13049]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 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: 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:0000377 abnormal hair follicle "malformed invagination of the epidermis from which the hair shaft develops" [J:65031]
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Allelic Composition: Fbxw4Dac/Fbxw4Dac,mdac/mdac
Genetic Background: involves: SM/Ckc

 MP:0000379 reduced hair follicle number "fewer number of the epidermal invaginations from which the hair shaft develops" [J:15108]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0000486 abnormal pulmonary trunk morphology "structural anomaly of the region of the pulmonary artery that arises from the right ventricle to the division of the right and left pulmonary artery" [Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8, hdene:Howard Dene, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0000488 abnormal intestinal epithelium morphology "anomalous structure or development of the cellular avascular layer of the digestive tube passing from the stomach to the anus" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Fgf10tm1Ska/Fgf10Tg(Myl3-lacZ)24Buck
Genetic Background: involves: C57BL/6 * CBA

 MP:0000495 abnormal colon morphology "malformation of the portion of the large intestine between the cecum and the rectum" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Fgf10tm1Ska/Fgf10Tg(Myl3-lacZ)24Buck
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Fgf10tm1.1(cre/ERT2)Sbel/Fgf10tm1.1(cre/ERT2)Sbel
Genetic Background: involves: 129 * C57BL/6J

 MP:0000537 abnormal urethra morphology "anomalous structure of the canal leading from the bladder, discharging the urine externally" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0000549 absent limbs "missing extremities" [J:51966, J:50768]
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Allelic Composition: Tnftm1Ljo/Tnf+
Genetic Background: involves: 129S1/Sv

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc,Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129S7/SvEvBrd * 129X1/SvJ

Allelic Composition: Fgf10Mhdaaey17/Fgf10Mhdaaey17
Genetic Background: C3HeB/FeJ-Fgf10Mhdaaey17

Allelic Composition: Fgf10tm1.1Sms/Fgf10tm1.1Sms,Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ

Allelic Composition: Fgf10ptls/Fgf10ptls
Genetic Background: involves: C57BL/6 * FVB/N

Allelic Composition: Fgf10tm1.1(cre/ERT2)Sbel/Fgf10tm1.1(cre/ERT2)Sbel
Genetic Background: involves: 129 * C57BL/6J

 MP:0000551 absent forelimb "missing the entire anterior extremities" [MGI:tc, J:54637]
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Allelic Composition: Tnftm1Ljo/Tnf+
Genetic Background: involves: 129S1/Sv

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 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: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0000557 absent hindlimb "missing the entire posterior extremities" [MGI:tc, J:54637]
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Allelic Composition: Tnftm1Ljo/Tnf+
Genetic Background: involves: 129S1/Sv

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0000571 interdigital webbing "fold of skin, or web, between the toes that is not normally present" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49840]
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Allelic Composition: Fgf10tm1.1(cre/ERT2)Sbel/Fgf10tm1.1(cre/ERT2)Sbel
Genetic Background: involves: 129 * C57BL/6J

 MP:0000592 short tail "reduced length of tail compared to control " [J:55583]
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Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc,Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129S7/SvEvBrd * 129X1/SvJ

Allelic Composition: Fgf10tm1.1Sms/Fgf10tm1.1Sms,Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ

 MP:0000614 absent salivary gland "missing any of the saliva-secreting glands of the oral cavity" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:tc, J:54637]
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Allelic Composition: Fbxw4Dac/Fbxw4Dac,mdac/mdac
Genetic Background: involves: SM/Ckc

 MP:0000644 dextrocardia "cardiac apex pointing to the right as opposed to the normal levocardia" [ava:Anna V. Anagnostopoulos, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0000662 abnormal branching of the mammary ductal tree "anomaly in the development of the channels that secrete milk and direct milk to the nipple" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 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: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0000762 abnormal tongue morphology "anomalous structure or development of the mobile mass of muscular tissue and surrounding epithelial tissue occupying the cavity of the mouth and forming part of the floor" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Lig4tm1Fwa/Lig4tm1Fwa,Trp53tm1Brd/Trp53+
Genetic Background: involves: 129S6/SvEvTac * 129S7/SvEvBrd

 MP:0000968 abnormal sensory neuron innervation "defective or incomplete supply of nerve fibers to sensory termini or to spinal cord" [J:31622]
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Allelic Composition: Cd19tm1(cre)Cgn/Cd19+,Ube2ntm1Aki/Ube2ntm1Aki
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0001145 abnormal male reproductive anatomy "anomalous structure of the organs associated with producing offspring in the gender that produces spermatozoa" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Lig4tm1Fwa/Lig4tm1Fwa,Trp53tm1Brd/Trp53+
Genetic Background: involves: 129S6/SvEvTac * 129S7/SvEvBrd

 MP:0001158 abnormal prostate morphology "mallformed gland in males that secretes part of the seminiferous fluid" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:63764]
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Allelic Composition: Lig4tm1Fwa/Lig4tm1Fwa,Trp53tm1Brd/Trp53+
Genetic Background: involves: 129S6/SvEvTac * 129S7/SvEvBrd

 MP:0001159 absent prostate gland "missing gland in males that secretes part of the seminiferous fluid" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:66126]
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Allelic Composition: Lig4tm1Fwa/Lig4tm1Fwa,Trp53tm1Brd/Trp53+
Genetic Background: involves: 129S6/SvEvTac * 129S7/SvEvBrd

 MP:0001176 abnormal lung development "malformation or arrest of differentiation of the organs of respiration" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:54931]
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Allelic Composition: Tnftm1Ljo/Tnf+
Genetic Background: involves: 129S1/Sv

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Fgf10tm1.1Sms/Fgf10tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Sms,Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+,Twist2tm1(cre)Dor/Twist2+
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * CBA

 MP:0001178 pulmonary hypoplasia "reduced size of the respiratory organ due to incomplete development of all or part of the organ " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Pathology , 2nd edition:ISBN 0-397-51047-0]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Sms,Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+,Twist2tm1(cre)Dor/Twist2+
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * CBA

 MP:0001181 absent lungs "missing organs of respiration" [J:51966, J:50768]
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Allelic Composition: Tnftm1Ljo/Tnf+
Genetic Background: involves: 129S1/Sv

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Fgf10tm1.1Sms/Fgf10tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

Allelic Composition: Fgf10ptls/Fgf10ptls
Genetic Background: involves: C57BL/6 * FVB/N

 MP:0001182 lung hemorrhage "bleeding in the respiratory organs" [J:66345]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Sms,Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+,Twist2tm1(cre)Dor/Twist2+
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * CBA

 MP:0001199 thin skin "reduced thickness of the outer protective layer of the body" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49471]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0001201 translucent skin "skin that is more transparent to light than normal " [J:15108]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0001216 abnormal epidermal layer morphology "anomalous structure or development of the superficial epithelial portion of the skin" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Lig4tm1Fwa/Lig4tm1Fwa,Trp53tm1Brd/Trp53+
Genetic Background: involves: 129S6/SvEvTac * 129S7/SvEvBrd

 MP:0001218 thin epidermis "reduced thickness of the superficial epithelial portion of the skin" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61790]
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Allelic Composition: Lig4tm1Fwa/Lig4tm1Fwa,Trp53tm1Brd/Trp53+
Genetic Background: involves: 129S6/SvEvTac * 129S7/SvEvBrd

 MP:0001262 decreased body weight "lower than normal average weight " [J:61295]
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Allelic Composition: Afg3l2Emv66/Afg3l2Emv66
Genetic Background: FVB.MEV2-Afg3l2Emv66

 MP:0001297 microphthalmia "reduced average size of the eyes" [J:18048]
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Allelic Composition: Esr1tm1Ksk/Esr1tm1Ksk
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N

 MP:0001302 eyelids open at birth "widely open eyes instead of closed at perinatal stage" [J:51966]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0001303 abnormal lens morphology "malformed transparent structure of the eye responsible for focusing light rays" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:40203]
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Allelic Composition: Esr1tm1Ksk/Esr1tm1Ksk
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N

 MP:0001312 abnormal cornea morphology "malformation or absence of the transparent anterior portion of the fibrous coat of the eye that serves as the chief refractory structure " [MeSH:National Library of Medicine - Medical Subject Headings , 2003, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Faddtm1e.1(KOMP)Wtsi/Faddtm1e.1(KOMP)Wtsi
Genetic Background: C57BL/6N-Faddtm1e.1(KOMP)Wtsi/Ucd

 MP:0001314 corneal opacity "complete or partial clouding of the cornea" [jte:Janan T. Eppig , Mouse Genome Informatics, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Faddtm1e.1(KOMP)Wtsi/Faddtm1e.1(KOMP)Wtsi
Genetic Background: C57BL/6N-Faddtm1e.1(KOMP)Wtsi/Ucd

 MP:0001556 increased circulating HDL cholesterol level "higher than average level of high density lipoprotein in the blood; this molecule transports cholesterol to the liver for excretion in bile" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:47439]
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Allelic Composition: Faddtm1e.1(KOMP)Wtsi/Faddtm1e.1(KOMP)Wtsi
Genetic Background: C57BL/6N-Faddtm1e.1(KOMP)Wtsi/Ucd

 MP:0001672 abnormal embryogenesis/ development "anomaly in the establishment of the characteristic configuration of the embryonic body" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Fgf10tm1.2Sms/Fgf10tm1.2Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ

Allelic Composition: Fgf10tm1Wss/Fgf10tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ

 MP:0002085 abnormal embryonic tissue morphology "structural abnormality or development of any embryonic tissue resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Fbxw4Dac/Fbxw4Dac,mdac/mdac
Genetic Background: involves: SM/Ckc

Allelic Composition: Fgf10tm1Ska/Fgf10Tg(Myl3-lacZ)24Buck
Genetic Background: involves: C57BL/6 * CBA

 MP:0002100 abnormal tooth morphology "atypical size, shape or hard tissue structure of the teeth " [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Fbxw4Dac/Fbxw4Dac,mdac/mdac
Genetic Background: involves: SM/Ckc

 MP:0002102 abnormal ear morphology "structural or developmental anomaly of any of the structures involved in the ear or vestibular system" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Fgf10tm1.2Sms/Fgf10tm1.2Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ

Allelic Composition: Fgf10tm1Wss/Fgf10tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ

 MP:0002132 abnormal respiratory system morphology "anomalous structure of pulmonary tissues " [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Fgf10tm1.2Sms/Fgf10tm1.2Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ

Allelic Composition: Fgf10tm1Wss/Fgf10tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ

 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: Fgf10tm1.2Sms/Fgf10tm1.2Sms,Fgf3tm1.2Sms/Fgf3tm1.2Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ

Allelic Composition: Fgf10tm1.2Sms/Fgf10tm1.2Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ

 MP:0002295 abnormal pulmonary circulation "anomalous circulation of blood through the lungs" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Fbxw4Dac/Fbxw4Dac,mdac/mdac
Genetic Background: involves: SM/Ckc

 MP:0002297 abnormal forced expiratory flow rates "anomaly in the rates of airflow during forced vital capacity determination" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Afg3l2Emv66/Afg3l2Emv66
Genetic Background: FVB.MEV2-Afg3l2Emv66

 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: 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:0002691 small stomach "reduced size of the stomach" [J:77398, dlb:Donna Burkart , Mouse Genome Informatics Curator]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0002729 abnormal canal morphology "any anomaly or malformation of the tubular ducts of the inner ear" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Cd19tm1(cre)Cgn/Cd19+,Ube2ntm1Aki/Ube2ntm1Aki
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0002770 absent bulbourethral gland "missing gland in males that lie along the prostate gland that secrete a fluid component of the seminal fluid into the urethra" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:78062]
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Allelic Composition: Lig4tm1Fwa/Lig4tm1Fwa,Trp53tm1Brd/Trp53+
Genetic Background: involves: 129S6/SvEvTac * 129S7/SvEvBrd

 MP:0002840 abnormal lens fibers morphology "structural anomaly of the elongated cells of the crystalline lens of the eye" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Esr1tm1Ksk/Esr1tm1Ksk
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N

Allelic Composition: Fgf10Mhdaaey17/Fgf10+
Genetic Background: involves: C3HeB/FeJ * C57BL/6

 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: 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:0002989 small kidney "reduced physical bulk one or both of the organs responsible for urine secretion" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0003014 abnormal kidney medulla morphology "anomalous structure of the inner portion of the kidney consisting of the renal pyramids" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:88636, smb:Susan M. Bello , Mouse Genome Informatics Curator]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0003051 curly tail "a loop or corkscrew-like curl in the tail" [csmith:Cynthia L. Smith, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc,Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129S7/SvEvBrd * 129X1/SvJ

 MP:0003124 hypospadia "a urethral opening located closer to the base of the penis and not at the tip" [smb:Susan M. Bello, Mouse Genome Informatics Curator, J:91491]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129X1/SvJ

 MP:0003162 reduced size of lateral semicircular canal 
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Allelic Composition: Cd19tm1(cre)Cgn/Cd19+,Ube2ntm1Aki/Ube2ntm1Aki
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0003163 absent posterior semicircular canal 
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Allelic Composition: Cd19tm1(cre)Cgn/Cd19+,Ube2ntm1Aki/Ube2ntm1Aki
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0003165 absent superior semicircular canal 
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Allelic Composition: Cd19tm1(cre)Cgn/Cd19+,Ube2ntm1Aki/Ube2ntm1Aki
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0003209 abnormal pulmonary elastic fiber morphology "malformation of a slender connective tissue fiber in pulmonary tissue characterized by great elasticity" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, RGD:Rat Genome Database submission]
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Allelic Composition: Fgf10tm1Ska/Fgf10Tg(Myl3-lacZ)24Buck
Genetic Background: involves: C57BL/6 * CBA

 MP:0003237 abnormal lens epithelium morphology "malformation in the one or more of the layers of epithelial cells in the lens" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:93301]
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Allelic Composition: Esr1tm1Ksk/Esr1tm1Ksk
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N

 MP:0003334 pancreatic fibrosis "invasion of fibrous connective tissue into the pancreas, often resulting from inflammation or injury " [MeSH:National Library of Medicine - Medical Subject Headings , 2003, ncbi:Matthew Mailman, NCBI request]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0003339 decreased number of pancreatic beta cells "fewer than normal number of the cells of the pancreas that secrete insulin" [ncbi:Matthew Mailman, NCBI request, MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0003358 abnormal hypaxial muscle morphology "malformation of the muscles of the limbs" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0003595 epididymal cyst "benign growths present in the elongated structure connected to the posterior surface of the testis that transports, stores, and matures spermatozoa between testis and vas deferens" [ncbi:Matthew Mailman, NCBI request]
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Allelic Composition: Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129X1/SvJ

 MP:0003641 small lung "reduced size of the lung relative to normal" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:95332]
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Allelic Composition: Fgf10tm1Ska/Fgf10Tg(Myl3-lacZ)24Buck
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Sms,Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+,Twist2tm1(cre)Dor/Twist2+
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * CBA

 MP:0003642 absent seminal gland "absence of the two folded, sac shaped, glands that is a diverticulum of the ductus deferens " [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129X1/SvJ

 MP:0003649 reduced right ventricle 
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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:0003755 abnormal palate "anomaly in the roof of the mouth in vertebrates formed anteriorly by a bony projection of the upper jaw (hard palate) and posteriorly by the fold of connective tissue (soft palate) " [ncbi:Matthew Mailman, NCBI request]
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Allelic Composition: Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129X1/SvJ

 MP:0003760 short palate "abnormally decreased length to the roof of the oral cavity" [ncbi:Matthew Mailman, NCBI request]
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Allelic Composition: Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129X1/SvJ

 MP:0003809 abnormal hair shaft morphology "irregular or unusual structure of the cuticle, and/or cortex and/or medulla of a hair" [llw2:Linda Washburn , Mouse Genome Informatics Curator]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0003827 abnormal Wolffian duct morphology "malformation of the transient embryonic tubes that empty into the cloca and degenerate in the male " [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129X1/SvJ

 MP:0003918 decreased kidney weight "reduced heft of the organs responsible for urine secretion" [RGD:Rat Genome Database submission]
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Allelic Composition: Fgf10tm1b(EUCOMM)Wtsi/Fgf10+
Genetic Background: C57BL/6N-Fgf10tm1b(EUCOMM)Wtsi/H

 MP:0003924 herniated diaphragm "protrusion of abdominal contents into the thoracic cavity through the diaphragm" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0003938 abnormal ear development "developmental anomaly of any of the structures involved in the ear or vestibular system" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Slc4a1tm1Llp/Slc4a1wan
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H/HeJ * C57BL/6J

 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: 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:0004140 abnormal chief cell morphology "malformation of the pepsinogen producing epithelial cells that are clustered at the base of the gastric gland " [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

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

 MP:0004200 reduced fetal size "smaller proportions of a fetus compared to littermates (sensu Mus: from E14 through birth)" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Tnftm1Ljo/Tnf+
Genetic Background: involves: 129S1/Sv

 MP:0004247 small pancreas "decrease of the size of the pancreas compared to controls" [MGI:monikat "Monika Tomczuk, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0004249 abnormal crista ampullaris morphology "anomaly in the elevation found on the inner surface of the ampullae of each semicircular duct; filaments of the vestibular nerve pass through the crista to reach hair cells on its surface; the hair cells are capped by the cupula, a gelatinous protein-polysaccharide mass" [J:60193, MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Cd19tm1(cre)Cgn/Cd19+,Ube2ntm1Aki/Ube2ntm1Aki
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0004309 absent otic vesicle "absence of the simple epithelial sac formed from the otic placode that gives rise to the structures of the inner ear" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc,Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129S7/SvEvBrd * 129X1/SvJ

Allelic Composition: Fgf10tm1.1Sms/Fgf10tm1.1Sms,Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ

 MP:0004310 small otic vesicle "reduced size of the simple epithelial sac formed from the otic placode that gives rise to the structures of the inner ear" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf3tm1Sng/Fgf3tm1Sng,Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * CBA

Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc,Fgf10tm1Wss/Fgf10+
Genetic Background: involves: 129S7/SvEvBrd * 129X1/SvJ

Allelic Composition: Fgf3tm1Mrc/Fgf3+,Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129S7/SvEvBrd * 129X1/SvJ

Allelic Composition: Fgf10tm1.1Sms/Fgf10tm1.1Sms,Fgf3tm1.1Sms/Fgf3tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * BALB/cJ

 MP:0004313 absent vestibulocochlear ganglion "absence of the group of neuron cell bodies associated with the eighth cranial nerve during embryogenesis; splits in later development to form the cochlear and vestibular ganglia" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf3tm1Sng/Fgf3tm1Sng,Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * CBA

 MP:0004317 small saccule "reduced size of the cavity between the semicircular canals and the cochlea of the inner ear" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Cd19tm1(cre)Cgn/Cd19+,Ube2ntm1Aki/Ube2ntm1Aki
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0004352 absent humerus "missing one or both of the bones of the forelimb that articulates with the scapula above and the radius and ulna below" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0004360 absent ulna "missing the medial and larger of the two bones of the forearm" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0004509 abnormal pelvic girdle bone morphology "any structural anomaly of the bones of the pelvis by which the limbs attach to the axial skeleton " [MGI:cwg "Carroll-Ann W. Goldsmith, Mouse Genome Informatics Curator"]
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Allelic Composition: Tnftm1Ljo/Tnf+
Genetic Background: involves: 129S1/Sv

 MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology "any structural anomaly or disruption of the typical staircase-like arrangement of the mechanosensitive hair bundles which are composed of thick long microvilli (stereocilia) and are located at the apical end of vestibular hair cells of the utricle and saccule" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Cd19tm1(cre)Cgn/Cd19+,Ube2ntm1Aki/Ube2ntm1Aki
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 MP:0004573 absent limb buds "missing 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: Tnftm1Ljo/Tnf+
Genetic Background: involves: 129S1/Sv

Allelic Composition: Fgf10ptls/Fgf10ptls
Genetic Background: involves: C57BL/6 * FVB/N

 MP:0004830 short incisors "reduced length of the long pointed teeth; most anterior and prominent in the jaw" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0004842 abnormal large intestine crypts of Lieberkuhn morphology "any structural anomaly in the tubular intestinal glands found in the mucosal membranes of the large intestine" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Fgf10tm1Ska/Fgf10Tg(Myl3-lacZ)24Buck
Genetic Background: involves: C57BL/6 * CBA

 MP:0004953 decreased spleen weight "reduction in the average weight of the organ that functions to filter blood and to store red corpuscles and platelets" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf10tm1b(EUCOMM)Wtsi/Fgf10+
Genetic Background: C57BL/6N-Fgf10tm1b(EUCOMM)Wtsi/H

 MP:0005287 narrow eye opening "less than the normal distance from one eyelid to the other " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, J:71350]
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Allelic Composition: Esr1tm1Ksk/Esr1tm1Ksk
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N

Allelic Composition: Fgf10tm1b(EUCOMM)Wtsi/Fgf10+
Genetic Background: C57BL/6N-Fgf10tm1b(EUCOMM)Wtsi/H

 MP:0005314 absent thyroid gland " missing endocrine gland that is normally located in the front and to the sides of the upper part of the trachea and which secretes thyroid hormone and calcitonin" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:30559]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0005315 absent pituitary gland "missing gland that is normally suspended from the base of the hypothalamus and which secretes somatotropins, prolactin, TSH (thyroid-stimulating hormone), gonadotropins, adrenal corticotropin" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:30559]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0005358 abnormal incisor morphology "structural defect of the long pointed teeth; most anterior and prominent in the jaw" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:85574]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0005584 abnormal enzyme/coenzyme activity "altered ability of any of these proteins, or their cofactors, to act as catalysts to induce chemical changes in other substances" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Fgf10tm1Ska/Fgf10Tg(Myl3-lacZ)24Buck
Genetic Background: involves: C57BL/6 * CBA

 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: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0006027 impaired alveologenesis "a block or reduction in the generation of alveoli" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:85546]
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Allelic Composition: Tnftm1Ljo/Tnf+
Genetic Background: involves: 129S1/Sv

 MP:0006030 abnormal otic vesicle formation "anomalous formation of the simple epithelial sac formed from the otic placode that gives rise to the structures of the inner ear" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:57313:]
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Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc,Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129S7/SvEvBrd * 129X1/SvJ

 MP:0006065 abnormal heart position "the heart is displaced from the normal left-sided position and/or orientation" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0006072 abnormal retinal apoptosis "increase or decrease in the number of cells in the retina undergoing programmed cell death" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:92622:]
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Allelic Composition: Fgf10Mhdaaey17/Fgf10+
Genetic Background: involves: C3HeB/FeJ * C57BL/6

 MP:0006090 abnormal utricle morphology "malformation in the larger of the two sacs in the vestibule" [smb:Susan M Bello, Mouse Genome Informatics Curator, Taber s Cyclopedic Medical Dictionary:19th edition: ISBN N 0-8036-0655-99, J:92940]
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Allelic Composition: Cd19tm1(cre)Cgn/Cd19+,Ube2ntm1Aki/Ube2ntm1Aki
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 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: 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:0006243 abnormal pupil dilation reaction to light "the pupil fails to constrict fully when exposed to bright light" [ncbi:Matthew Mailman, NCBI request, smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Fgf10tm1b(EUCOMM)Wtsi/Fgf10+
Genetic Background: C57BL/6N-Fgf10tm1b(EUCOMM)Wtsi/H

 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: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0006285 absent inner ear "absence of all components of the labyrinth, including the semicircular canals, vestibule and cochlea" [J:86619, MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf3tm1Mrc/Fgf3tm1Mrc,Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129S7/SvEvBrd * 129X1/SvJ

 MP:0006288 small otic capsule "reduced size of the cartilage or bony capsule surrounding the inner ear mechanism" [J:59285, MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 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: 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: 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: 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:0006402 small molars "reduced size of the most posterior teeth located on either side of the jaw, and characterized by a large crown and broad chewing surface" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0008320 absent adenohypophysis "absence of the anterior part of the pituitary that secretes a variety of hormones" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0008786 abnormal hindgut morphology "any structural anomaly of the caudal portion of the primitive digestive tube of the embryo" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

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

 MP:0008904 abnormal mammary fat pad morphology "any structural anomaly of the encapsulated adipose tissue associated with the mammary gland" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0009479 abnormal cecum development "malformation or aberrant differentiation of the large sac at the ileum and large intestine junction" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129X1/SvJ * C57BL/6

Allelic Composition: Fgf10tm1.1(cre/ERT2)Sbel/Fgf10tm1Sms,Gt(ROSA)26Sortm9(CAG-tdTomato)Hze/Gt(ROSA)26Sor+
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6

 MP:0009509 absent rectum "absence or loss of the terminal portion of the intestinal tube adjacent to the anus" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0009510 cecal atresia "congenital blockage or absence of the lumen of the cecum" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Fgf10tm1.1(cre/ERT2)Sbel/Fgf10tm1.1(cre/ERT2)Sbel
Genetic Background: involves: 129 * C57BL/6J

 MP:0009520 decreased submandibular gland size "reduced size of either of the large major salivary glands situated beneath the mandible" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Cer1tm1Bhr/Cer1tm1Bhr,Lefty1tm1Sla/Lefty1tm1Sla
Genetic Background: involves: 129S7/SvEvBrd * CD-1

 MP:0009522 submandibular gland hypoplasia "underdevelopment or reduced size of either of the large major salivary glands situated beneath the mandible, usually due to reduced cell number" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Fgf10tm1Ska/Fgf10+
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Fgf10tm1Wss/Fgf10+
Genetic Background: involves: 129 * 129X1/SvJ * BALB/c * C57BL/6

 MP:0009524 absent submandibular gland "absence of either of the large major salivary glands situated beneath the mandible" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0009525 abnormal submandibular duct morphology "any strucutral anomaly of the duct of the submadibular gland that opens at the sublingual papilla near the frenulum of the tongue" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Fgf10tm1Ska/Fgf10+
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Fgf10tm1Wss/Fgf10+,Fgfr2tm2Dsn/Fgfr2+,Tg(Pgk1-cre)1Lni/0
Genetic Background: involves: 129 * 129X1/SvJ * BALB/c * C57BL/6

 MP:0009571 abnormal right lung accessory lobe morphology 
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Sms,Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+,Twist2tm1(cre)Dor/Twist2+
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * CBA

 MP:0009572 abnormal right lung cranial lobe morphology 
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Sms,Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+,Twist2tm1(cre)Dor/Twist2+
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * CBA

 MP:0009573 abnormal right lung middle lobe morphology 
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Sms,Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+,Twist2tm1(cre)Dor/Twist2+
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * CBA

 MP:0009655 abnormal secondary palate development "any anomaly in the formation of the part of the palate that is formed during embryonic development when palatal projections from the inner part of the maxillary processes emerge, extend and elevate into a horizontal position above the tongue" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator", PMID:16942766]
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Allelic Composition: Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129X1/SvJ

 MP:0009884 palatal shelf fusion with tongue or mandible "palatal shelves do not elevate during development and instead fuse with tongue tissues or with the mandible tissues" [PMID:16680722]
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Allelic Composition: Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129X1/SvJ

 MP:0009890 cleft secondary palate "congenital fissure of the tissues normally uniting to form the secondary palate" [PMID:16680722]
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Allelic Composition: Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129X1/SvJ

 MP:0010024 increased total body fat amount "greater than the normal total amount of connective tissue composed of fat cells within the entire body" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf10tm1b(EUCOMM)Wtsi/Fgf10+
Genetic Background: C57BL/6N-Fgf10tm1b(EUCOMM)Wtsi/H

 MP:0010053 decreased grip strength "reduced ability to grasp and hold objects, often measured as time spent hanging from an object or wire" [ISBN:0471316393 "Crawley, JN, What s Wrong with my Mouse: Behavioral Phenotyping of Transgenic and Knockout Mice"]
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Allelic Composition: Fgf10tm1b(EUCOMM)Wtsi/Fgf10+
Genetic Background: C57BL/6N-Fgf10tm1b(EUCOMM)Wtsi/H

 MP:0010116 abnormal primitive urogenital sinus morphology "any structural anomaly of the ventral part of the cloaca remaining after septation of the rectum, which further develops into part of the bladder, part of the prostatic part of the male urethra and the urethra and vestibule in females" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129X1/SvJ

 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: 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: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: 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:0010489 abnormal heart atrium auricular region morphology "any structural anomaly of the small conical pouch projections located on the upper anterior portion of each atrium of the heart" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0010521 absent pulmonary artery "absence of the artery that arises from the right ventricle and conveys unaerated blood to the lungs" [MESH:A07.231.114.715]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0010646 absent pulmonary vein "absence of the veins that return oxygenated blood from the lungs to the left atrium of the heart" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0010681 abnormal hair follicle bulb morphology "any structural anomaly of the thickened portion of the proximal portion of the hair follicle that contains rapidly proliferating matrix cells, melanocytes and outer root sheath cells" [PMID:19211055]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0010794 abnormal stomach submucosa morphology "any structural anomaly of the fibrous connective tissue layer beneath the stomach mucosa" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0010906 abnormal lung bud morphology "any structural anomaly of the primary outgrowth of the embryonic trachea i.e. blunt end of the respiratory diverticulum which grows ventrally out of the proximal end of the foregut, then extends caudally and divides into two, forming the anlage of a primary bronchus and all its branches" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf10tm1.1(cre/ERT2)Sbel/Fgf10tm1Sms,Gt(ROSA)26Sortm9(CAG-tdTomato)Hze/Gt(ROSA)26Sor+
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6

 MP:0010907 absent lung buds "absence of the blunt end of the respiratory diverticulum which normally grows ventrally out of the proximal end of the foregut, then extends caudally and divides into two, forming the origins of the bronchial tree" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Fgf10tm1.1(cre/ERT2)Sbel/Fgf10tm1.1(cre/ERT2)Sbel
Genetic Background: involves: 129 * C57BL/6J

 MP:0010975 abnormal lung lobe morphology "any structural anomaly of any of the anatomically and functionally distinct subunits (lobes) comprising the left or right lung, where each lobe receives air from its own secondary bronchus and is separated from it neighbors by one or more fissures (walls of connective tissue)" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Sms,Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+,Twist2tm1(cre)Dor/Twist2+
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * CBA

 MP:0010976 small lung lobe "reduced size of any of the anatomically and functionally distinct subunits (lobes) comprising the left or right lung, where each lobe receives air from its own secondary bronchus and is separated from it neighbors by one or more fissures (walls of connective tissue)" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Sms,Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+,Twist2tm1(cre)Dor/Twist2+
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * CBA

 MP:0011025 abnormal branching involved in trachea morphogenesis "anomaly in the process in which the two main branches of the trachea is generated and organized" [MGI:csmith]
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Allelic Composition: Tnftm1Ljo/Tnf+
Genetic Background: involves: 129S1/Sv

 MP:0011028 impaired branching involved in bronchus morphogenesis 
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Allelic Composition: Tnftm1Ljo/Tnf+
Genetic Background: involves: 129S1/Sv

Allelic Composition: Fgf10tm1Ska/Fgf10Tg(Myl3-lacZ)24Buck
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Sms,Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+,Twist2tm1(cre)Dor/Twist2+
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * CBA

 MP:0011030 impaired branching involved in preterminal bronchiole morphogenesis 
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Allelic Composition: Tnftm1Ljo/Tnf+
Genetic Background: involves: 129S1/Sv

 MP:0011064 abnormal vestibular hair cell kinocilium morphology "any structural anomaly of the nonmotile primary cilium that is found at the apical surface of vestibular hair cells" [GO:0060091, MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Cd19tm1(cre)Cgn/Cd19+,Ube2ntm1Aki/Ube2ntm1Aki
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

 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: Fgf10tm1.1Sms/Fgf10tm1.1Sms
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 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: Tnftm1Ljo/Tnf+
Genetic Background: involves: 129S1/Sv

Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0011091 complete prenatal lethality "death of all organisms of a given genotype in a population between fertilization and birth (Mus: approximately E18.5)" [MGI:csmith]
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Allelic Composition: Fgf10Mhdaaey17/Fgf10Mhdaaey17
Genetic Background: C3HeB/FeJ-Fgf10Mhdaaey17

 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: Fgf3tm1Sng/Fgf3tm1Sng,Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * CBA

 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:0011195 increased hair follicle apoptosis "greater than expected levels of programmed cell death of cells in the epidermis from which the hair shaft develops" [MGI:mnk]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0011305 dilated kidney calyx "an expansion in the lumen volume or area of any of the branches of the renal pelvis that surround each renal papilla and collect urine" [MGI:anna]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0011332 abnormal kidney outer medulla morphology "any structural anomaly of the outer medullary region of the adult kidney containing the short Loops of Henle and collecting ducts" [MGI:csmith, PMID:20614633]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0011333 abnormal kidney inner medulla morphology "any structural anomaly of the inner medullary region of the adult kidney containing collecting ducts and the long loops of Henle" [MGI:csmith, PMID:20614633]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0011457 abnormal metanephric ureteric bud development "any anomaly in the development of the portion of the ureteric bud tube that contributes to the morphogenesis of the metanephros" [GO:0035502]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0011759 absent Rathke s pouch "absence of the diverticulum arsing from the embryonic buccal cavity from which the anterior lobe of the pituitary gland is developed" [MGI:anna]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0011884 absent colon "absence of the portion of the large intestine between the cecum and the rectum" [MGI:Colin_McKerlie]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

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

 MP:0013264 tongue ankylosis "partial or complete fusion or adherence of the tongue to the floor of the mouth, resulting in varying degrees of restricted tongue mobility; partial ankyloglossia (aka tongue-tie) is caused by a lingual frenulum that is abnormally short or is attached too close to the tip of the tongue; in complete ankyloglossia the tongue is tethered to the floor of the mouth" [MGI:anna]
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Allelic Composition: Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129X1/SvJ

 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:0013338 abnormal neurohypophysis development "aberrant formation or incomplete differentiation of the posterior lobe of the pituitary gland which develops as a neurohypophyseal bud, a depression in the neuroectoderm of the floor of the hypothalamus; the infundibulum, another diverticulum from the inferior aspect of the diencephalon, develops as an outgrowth of the neurohypophyseal bud and connects the neurohypophysis to the hypothalamus; the neurohypophysis develops as the infundibulum grows inferiorly from the diencephalon to meet the developing adenohypophysis (anterior pituitary lobe); the fully developed neurohypophysis consists of the infundibulum and the pars nervosa; the neural connection between the hypothalamus and pars nervosa is through the hypothalamohypophyseal tract that develops within the infundibulum" [MGI:Anna]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0013352 abnormal Rathke s pouch apoptosis "any change in the timing or number of Rathke s pouch cells undergoing programmed cell death" [MGI:Anna]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0013445 Harderian gland atrophy "acquired diminution of the size of the sebaceous gland that is located behind the eyeball and excretes fluid that facilitates movement of the nictitating membrane, associated with wasting as from death and reabsorbtion of cells, diminished cellular proliferation, decreased cellular volume, pressure, ischemia, malnutrition, reduced function or malfunction, or hormonal changes" [MGI:Anna]
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Allelic Composition: Esr1tm1Ksk/Esr1tm1Ksk
Genetic Background: involves: 129P2/OlaHsd * C57BL/6N

 MP:0013495 decreased trachea gland number "fewer than normal numbers of the tubuloacinar seromucous glands which are principally located in the submucosa of the trachea, open into the tracheal lumen through short ducts, and secrete mucus, lysozyme, defensins, and other agents that help protect the lungs from particles and infectious agents; in the mouse, they are restricted to the upper trachea, more specifically to the regions between the first few cartilage rings, with the precise distribution depending on genetic background" [http://medical-dictionary.thefreedictionary.com/tracheal+glands, ISBN:1451113412, MGI:Anna, PMID:15973734]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0013531 abnormal periderm development "abnormal formation of the outermost layer of the bilaminar embryonic/fetal epidermis; periderm cells emerge at approximately E9.5 and form simple squamous epithelium, the most superficial embryonic layer; these cells form the first, but temporary, embryonic permeability barrier, and are replaced by the cornified envelope, that forms during keratinocyte stratification, by E16.5" [http://discovery.lifemapsc.com/in-vivo-development/epidermis/embryonic-epidermis/periderm-cells, MGI:Anna]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

 MP:0013580 abnormal nasal gland morphology "any structural anomaly of any of the seromucous glands found in the respiratory region of the nasal mucous membrane, including anterior serous glands, seromucous glands, and Bowman glands" [http://en.wikipedia.org/wiki/Nasal_glands, MGI:Anna, UBERON:0012278]
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Allelic Composition: Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129X1/SvJ

Allelic Composition: Fgf10tm1Wss/Fgf10+
Genetic Background: involves: 129X1/SvJ

 MP:0013582 abnormal lateral nasal gland morphology "any structural anomaly of the lateral nasal glands (the largest nasal secretory glands in rodents) which surround the maxillary sinus located in the lateral wall adjacent to each nasal passage and are characterized by cytologic features similar to those described for the major serous salivary glands; secretory contents of the LNG drain into the nasal vestibule; the LNG is a major site for the synthesis and secretion of odorant-binding proteins that serve as odorant carriers in nasal mucus; it also, synthesizes large amounts of immunoglobulin A, which is important for immune defense of the upper respiratory tract, and testosterone and salivary androgen-binding proteins, which are likely important in olfaction and reproductive behavior" [ISBN:0080454321, ISBN:0123813611, MGI:Anna]
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Allelic Composition: Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129X1/SvJ

Allelic Composition: Fgf10tm1Wss/Fgf10+
Genetic Background: involves: 129X1/SvJ

 MP:0013721 abnormal mammary placode morphology "any structural anomaly of the transient lens-shaped thickening of surface ectoderm that will give rise to the mammary bud proper; in mouse, five pairs of symmetrically positioned mammary placodes (three thoracic and two inguinal) form at reproducible locations along the mammary line at E11.5; the individual pairs develop asynchronously and in a distinct order; pair 3 is first, followed by pair 4, then by pairs 1 and 5 (which develop together), and finally by pair 2; the orientation of placodal cells is not uniform, suggesting that placodes are formed by migration of cells from the mammary line; between E11.5 and E12.5, each mammary placode expands and invaginates into the underlying mesenchyme to form an early bulb-shaped mammary bud " [PMID:16168142, PMID:20484386]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

Allelic Composition: Fgf10tm1Ska/Fgf10Tg(Myl3-lacZ)24Buck
Genetic Background: involves: C57BL/6 * CBA

 MP:0013766 absent palatal rugae "absence of the transverse folds (ridges) of the mucosa located on the anterior third part of the secondary (hard) palate of most mammalian species" [MGI:Anna, PMID:19087265]
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Allelic Composition: Fgf10tm1Wss/Fgf10tm1Wss
Genetic Background: involves: 129X1/SvJ

 MP:0013956 decreased colon length "reduced length of the portion of the large intestine between the cecum and the rectum" [ISBN:0683400088]
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Allelic Composition: Fgf10tm1Ska/Fgf10tm1Ska
Genetic Background: involves: C57BL/6 * CBA

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSMUSG00000048373 Fgfbp1 / O70514 / Fibroblast growth factor-binding protein 1 / Q14512*  / complex / reaction






 

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