ENSMUSG00000017491


Mus musculus

Features
Gene ID: ENSMUSG00000017491
  
Biological name :Rarb
  
Synonyms : P22605 / Rarb / retinoic acid receptor, beta
  
Possible biological names infered from orthology : P10826
  
Species: Mus musculus
  
Chr. number: 14
Strand: -1
Band: A2
Gene start: 16430839
Gene end: 16819156
  
Corresponding Affymetrix probe sets: 10417713 (MoGene1.0st)   1454906_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000067694
Ensembl peptide - ENSMUSP00000153519
Ensembl peptide - ENSMUSP00000153454
Ensembl peptide - ENSMUSP00000153178
Ensembl peptide - ENSMUSP00000153098
Ensembl peptide - ENSMUSP00000152980
NCBI entrez gene - 218772     See in Manteia.
MGI - MGI:97857
RefSeq - NM_011243
RefSeq - NM_001289760
RefSeq - NM_001289761
RefSeq - NM_001289762
RefSeq Peptide - NP_001276689
RefSeq Peptide - NP_001276690
RefSeq Peptide - NP_001276691
RefSeq Peptide - NP_035373
swissprot - Q6DFX0
swissprot - A0A286YDP5
swissprot - A0A286YCX1
swissprot - A0A286YCR2
swissprot - A0A286YCH1
swissprot - P22605
swissprot - A0A286YE15
Ensembl - ENSMUSG00000017491
  

This gene has been taged as a transcription factor by TFT
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 RARBENSGALG00000011298Gallus gallus
 RARBENSG00000077092Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Rara / P11416 / retinoic acid receptor, alpha / P10276*ENSMUSG0000003799274
Rarg / P18911 / Retinoic acid receptor gamma / P13631*ENSMUSG0000000128873
Thra / P63058 / Thyroid hormone receptor alpha / P10827*ENSMUSG0000005875630
Thrb / P37242 / Thyroid hormone receptor beta / P10828*ENSMUSG0000002177929
Nr1h2 / Q60644 / Oxysterols receptor LXR-beta / P55055* / nuclear receptor subfamily 1 group H member 2*ENSMUSG0000006060128
Nr1h4 / Q60641 / Bile acid receptor / Q96RI1* / nuclear receptor subfamily 1 group H member 4*ENSMUSG0000004763827
Nr1h3 / Q9Z0Y9 / Mus musculus nuclear receptor subfamily 1, group H, member 3 (Nr1h3), transcript variant 3, mRNA. / Q13133* / nuclear receptor subfamily 1 group H member 3*ENSMUSG0000000210827
Nr1i2 / O54915 / Nuclear receptor subfamily 1 group I member 2 / O75469*ENSMUSG0000002280926
Nr1h5ENSMUSG0000004893824
Vdr / P48281 / vitamin D (1,25-dihydroxyvitamin D3) receptor / P11473* / vitamin D receptor*ENSMUSG0000002247923
Nr1i3 / O35627 / Nuclear receptor subfamily 1 group I member 3 / Q14994*ENSMUSG0000000567722


Protein motifs (from Interpro)
Interpro ID Name
 IPR000536  Nuclear hormone receptor, ligand-binding domain
 IPR001628  Zinc finger, nuclear hormone receptor-type
 IPR001723  Nuclear hormone receptor
 IPR003078  Retinoic acid receptor
 IPR013088  Zinc finger, NHR/GATA-type
 IPR035500  Nuclear hormone receptor-like domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0000122 negative regulation of transcription by RNA polymerase II IDA
 biological_processGO:0001657 ureteric bud development IMP
 biological_processGO:0002068 glandular epithelial cell development IGI
 biological_processGO:0003148 outflow tract septum morphogenesis IGI
 biological_processGO:0003406 retinal pigment epithelium development IGI
 biological_processGO:0003417 growth plate cartilage development IGI
 biological_processGO:0006351 transcription, DNA-templated IEA
 biological_processGO:0006355 regulation of transcription, DNA-templated IEA
 biological_processGO:0008284 positive regulation of cell proliferation IGI
 biological_processGO:0008285 negative regulation of cell proliferation IGI
 biological_processGO:0021756 striatum development IMP
 biological_processGO:0022008 neurogenesis IMP
 biological_processGO:0031641 regulation of myelination IEA
 biological_processGO:0032331 negative regulation of chondrocyte differentiation IMP
 biological_processGO:0035116 embryonic hindlimb morphogenesis IGI
 biological_processGO:0035264 multicellular organism growth IGI
 biological_processGO:0043065 positive regulation of apoptotic process IGI
 biological_processGO:0043066 negative regulation of apoptotic process IGI
 biological_processGO:0043068 positive regulation of programmed cell death IGI
 biological_processGO:0043401 steroid hormone mediated signaling pathway IEA
 biological_processGO:0045666 positive regulation of neuron differentiation IEA
 biological_processGO:0045944 positive regulation of transcription by RNA polymerase II IGI
 biological_processGO:0048048 embryonic eye morphogenesis IGI
 biological_processGO:0048384 retinoic acid receptor signaling pathway IEA
 biological_processGO:0048566 embryonic digestive tract development IEA
 biological_processGO:0055012 ventricular cardiac muscle cell differentiation IMP
 biological_processGO:0060041 retina development in camera-type eye IGI
 biological_processGO:0060348 bone development IGI
 biological_processGO:0061037 negative regulation of cartilage development IMP
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005654 nucleoplasm IEA
 molecular_functionGO:0000977 RNA polymerase II regulatory region sequence-specific DNA binding IDA
 molecular_functionGO:0003677 DNA binding IEA
 molecular_functionGO:0003700 DNA-binding transcription factor activity IEA
 molecular_functionGO:0003707 steroid hormone receptor activity IEA
 molecular_functionGO:0003708 retinoic acid receptor activity IEA
 molecular_functionGO:0008144 drug binding IEA
 molecular_functionGO:0008270 zinc ion binding IEA
 molecular_functionGO:0043565 sequence-specific DNA binding IEA
 molecular_functionGO:0046872 metal ion binding IEA
 molecular_functionGO:0046965 retinoid X receptor binding IEA


Pathways (from Reactome)
Pathway description
Nuclear Receptor transcription pathway
Signaling by Retinoic Acid


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000079 abnormal basioccipital bone morphology "malformed basilar process of the occipital bone" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:55583]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarb+,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rarg+
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0000137 abnormal vertebrae morphology "malformed bony segment of the spinal column" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarb+,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0000157 abnormal sternum morphology "malformed long flat bone of the chest; articulates with clavicle and first seven rib pairs" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:19212]
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Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarb+
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rarg+
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0000159 abnormal xiphoid process "malformed posterior tip of the sternum" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:42932]
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Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0000163 abnormal cartilage morphology "anomalous structure or development of the nonvascular, resilient, flexible connective tissue found primarily in joints, walls of the throax, and tubular structures, but which also comprises most of the skeleton in early fetal life " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Raratm1Ipc/Rara+,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0000468 abnormal esophageal epithelium morphology "malformation of the epithelial layer of the esophagus" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:tc]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

 MP:0000471 abnormal stomach epithelium morphology "malformation of the epithelial layer of the stomach " [tc:Teresa Chu , Mouse Genome Informatics Curator]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

 MP:0000484 abnormal pulmonary artery morphology "structrual anomaly of the artery that arises from the right ventricle and conveys unaerated blood to the lungs " [MeSH:National Library of Medicine - Medical Subject Headings, 2003, hdene:Howard Dene, Mouse Genome Informatics Curator]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0000519 hydronephrosis "dilation of the pelvis and calices of one or both kidneys" [J:56641]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 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: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

 MP:0000534 abnormal ureter morphology "anomalous structure of the tube that conducts the urine from the renal pelvis to the bladder" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0000536 hydroureter "distention of the ureter with urine, due to blockage from any cause" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:Cml, J:13044]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

 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: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0001076 abnormal hypoglossal nerve morphology "malformation or misprojection of motor axons to the tongue" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:45302]
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Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0001119 abnormal female reproductive anatomy "anomalous structure of the organs associated with producing offspring in the gender that bears the offspring" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

 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: Mapk7tm1Kda/Mapk7tm1Kda
Genetic Background: involves: 129S6/SvEvTac

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 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: Raratm1Ipc/Raratm1Ipc,Rarbtm1Ipc/Rarb+
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0001262 decreased body weight "lower than normal average weight " [J:61295]
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Allelic Composition: Mapk7tm1Kda/Mapk7tm1Kda
Genetic Background: involves: 129S6/SvEvTac

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0001286 abnormal eye development "malformation or arrest of differentiation of the visual organ" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:49840]
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Allelic Composition: Aldh1a1tm1.1Ngb/Aldh1a1tm1.1Ngb,Aldh1a3tm1.1Pcn/Aldh1a3tm1.1Pcn
Genetic Background: involves: 129/Sv * C57BL/6 * SJL

 MP:0001289 persistence of hyaloid capillary system "failure of the degeneration of the transient vascular system of the eye during development" [J:49840]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 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: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0001304 cataracts "complete or partial opacity of the lens" [J:65031]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0001325 abnormal retina morphology "structural or developmental anomaly of the thin layer of neural tissue lining the back of the eyeball which contains visual receptors " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0001463 abnormal spatial learning "defects in the abilibity to navigate using behavioraly meaningful locations" [CFG:Center for Functional Genomics , Northwestern University]
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Allelic Composition: Mapk7tm1Kda/Mapk7tm1Kda
Genetic Background: involves: 129S6/SvEvTac

Allelic Composition: Rarbtm1Vgi/Rarbtm1Vgi,Rxrbtm1Rev/Rxrbtm1Rev
Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6

 MP:0001473 reduced long term potentiation "less than the normal persistent robust synaptic response induced by synchronous stimulation of pre- and postsynaptic cells " [Principles of Neural Science:ISBN 0-8385-8034-3]
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Allelic Composition: Mapk7tm1Kda/Mapk7tm1Kda
Genetic Background: involves: 129S6/SvEvTac

Allelic Composition: Rarbtm1Vgi/Rarbtm1Vgi,Rxrbtm1Rev/Rxrbtm1Rev
Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6

 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: Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0001899 absent long term depression "lack of the normal, persistent activity-dependent decrease in synaptic efficacy between neurons, often following slow, weak stimulation of CA1 neurons" [Principles of Neural Science:ISBN 0-8385-8034-3, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Mapk7tm1Kda/Mapk7tm1Kda
Genetic Background: involves: 129S6/SvEvTac

Allelic Composition: Rarbtm1Vgi/Rarbtm1Vgi,Rxrbtm1Rev/Rxrbtm1Rev
Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6

 MP:0002081 perinatal lethality "death anytime between E18.5 and postnatal day 1 " [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Raratm2Ipc/Raratm2Ipc,Raratm1Ipc/Rara+,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas

 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: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

 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: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Ipc/Rarb+
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

 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: Raratm3.1Ipc/Raratm3.1Ipc
Genetic Background: involves: 129/Sv * C57BL/6 * SJL

 MP:0002191 abnormal artery morphology "malformation of the blood vessels that carry blood away from the heart" [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: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0002257 abnormal arytenoid cartilage morphology "any structural anomaly of the paired triangular cartilages located postlaterally at the level of the thyroid cartilage " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Pathology , 2nd edition:ISBN 0-397-51047-0]
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Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0002258 abnormal cricoid cartilage morphology "any structural anomaly of the most inferior of the laryngeal cartilages " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Pathology , 2nd edition:ISBN 0-397-51047-0]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarb+,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0002260 abnormal thyroid cartilage morphology "any structural anomaly of the largest of the laryngeal cartilages " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Pathology , 2nd edition:ISBN 0-397-51047-0]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarb+
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0002265 abnormal left major bronchus morphology "any structural anomaly of the conducting airway leading to the left lobe of the lungs" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Pathology , 2nd edition:ISBN 0-397-51047-0]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

 MP:0002266 abnormal right major bronchus morphology "any structual anomaly of the conducting airway leading to the right lobe of the lungs " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Pathology , 2nd edition:ISBN 0-397-51047-0]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

 MP:0002271 abnormal alveolar duct morphology "any structural anomaly of the conducting tubes leading to the alveoli " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Mapk7tm1Kda/Mapk7tm1Kda
Genetic Background: involves: 129S6/SvEvTac

 MP:0002327 abnormal respiratory function "anomaly in any measure of the processes involved in respiration" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Mapk7tm1Kda/Mapk7tm1Kda
Genetic Background: involves: 129S6/SvEvTac

 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: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Ipc/Rarb+
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0002699 abnormal vitreous body "anomalies of the transparent, semigelatinous substance that fills the cavity behind the crystalline lens of the eye and in front of the retina" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0002703 abnormal renal tubules "anomalous structure or development of the loops of Henle and collecting ducts in the kidney" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Ipc/Rarb+
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

 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: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0002912 abnormal excitatory postsynaptic potential "defect in the potential detected in postsynaptic cells when an excitatory impulse arrives at the synapse causing depolarization" [Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3]
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Allelic Composition: Mapk7tm1Kda/Mapk7tm1Kda
Genetic Background: involves: 129S6/SvEvTac

Allelic Composition: Rarbtm1Vgi/Rarbtm1Vgi,Rxrbtm1Rev/Rxrbtm1Rev
Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6

 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: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

 MP:0003036 vertebral transformation "homeotic transformation of a specific vertebrae to adopt the fate of another" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarb+
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarb+,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0003120 abnormal tracheal cartilage "any structural anomaly of the cartilaginous structures that support the trachea" [smb:Susan M. Bello, Mouse Genome Informatics Curator, J:97123]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Rarbtm1Ipc/Rarbtm1Ipc,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarb+
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarb+,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0003182 decreased pulmonary endothelial cell surface 
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Allelic Composition: Mapk7tm1Kda/Mapk7tm1Kda
Genetic Background: involves: 129S6/SvEvTac

 MP:0003321 tracheoesophageal fistula "an abnormal passage between the esophagus and the trachea, acquired or congenital, often associated with esophageal atresia" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, ncbi:Matthew Mailman, NCBI request]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0003446 renal hypoplasia "decreased cell number in the kidney leading to reduced size" [llw2:Linda Washburn , Mouse Genome Informatics Curator]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Ipc/Rarb+
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0003558 absent uterus "absence of the female muscular organ of gestation" [ncbi:Matthew Mailman, NCBI request]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0003575 absent oviduct "absence of the tube through which the ova pass from the ovary to the uterus" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0003600 ectopic kidney 
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Ipc/Rarb+
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

 MP:0003604 single kidney 
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Allelic Composition: Taf4tm1Idvd/Taf4tm1Idvd,Tg(KRT14-cre/ERT2)1Ipc/0
Genetic Background: involves: C57BL/6 * SJL

 MP:0003869 ectopic cartilage "positional abnormality of cartilage" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

 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: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * 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: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0004423 abnormal squamosal bone morphology "any structural anomaly of the thin, platelike part of the temporal bone" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarb+
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0004599 abnormal vertebral arch morphology "any structural anomaly of the dorsal part of a vertebra, consisting of a pair of pedicles, a pair of laminae, and seven processes (four articular processes, two transverse processes, and one spinous process)" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0004613 fusion of vertebral arches "improper union of the dorsal part of adjacent vertebra" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarb+
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarb+,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0004615 cervical vertebral transformation "homeotic transformation of any cervical vertebrae to adopt the fate of another vertebrae" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarb+
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Rara+,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarb+,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0004616 lumbar vertebral transformation "homeotic transformation of any lumbar vertebrae to adopt the fate of another vertebrae" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0004618 thoracic vertebral transformation "homeotic transformation of any thoracic vertebrae to adopt the fate of another vertebrae" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarb+
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarb+,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0004666 absent stapedial artery "absence of the small artery that passes through the ring of the stapes" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 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: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

 MP:0005106 abnormal incus morphology "structural anomaly of the middle of the three auditory ossicles" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:83132]
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Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarb+
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0005107 abnormal stapes morphology "structural anomaly of the smallest and innermost of the three auditory ossicles" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:83132]
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Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0005205 abnormal eye anterior chamber "anomaly of the space in the eye, filled with aqueous humor, and bounded anteriorly by the cornea and a small portion of the sclera and posteriorly by a small portion of the ciliary body, the iris, and part of the crystalline lens" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0005208 abnormal iris stroma morphology "structural anomaly of the lamellated connective tissue of the iris" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 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: Scn5atm1Clhh/Scn5a+
Genetic Background: involves: 129 * 129S/SvEv * C57BL/6J

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarb+,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0005300 abnormal corneal stroma morphology "structural anomaly of the lamellated connective tissue of the cornea" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0005508 abnormal skeleton morphology "malformation of the bony framework of the body in vertebrates" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarb+
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Rara+,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarb+,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rarg+
Genetic Background: involves: 129S2/SvPas * C57BL/6

 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: Mapk7tm1Kda/Mapk7tm1Kda
Genetic Background: involves: 129S6/SvEvTac

 MP:0006063 abnormal inferior vena cava morphology "structural malformation in the principal vein draining blood from the lower portion of the body" [smb:Susan M Bello, Mouse Genome Informatics Curator, Taber s Cyclopedic Medical Dictionary:19th edition: ISBN N 0-8036-0655-99]
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Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0006069 abnormal retinal neuronal layer morphology "malformation in any of the neuronal layers that make up the retina, including the ganglion cell, inner plexiform, inner nuclear, outer plexiform, outer nuclear layers, the inner and outer segments" [smb:Susan M Bello, Mouse Genome Informatics Curator, Gray s Anatomy:ISBN 0-914294-08-3]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0006200 vitreous body deposition "abnormal accumulation of material in the vitreous body" [ncbi:Matthew Mailman, NCBI request, smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 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: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

 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: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

 MP:0006425 absent Mullerian ducts "absence of the transient embryonic drainage tubes of the embryonic kidney (mesonephric tubules) that empty into the cloaca and in the female develop into the oviducts, uterus, and vagina" [J:40605, MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0008380 abnormal gonial bone morphology "any structural abnormality of the investing bone that lies on the surface of the malleus" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0008514 absent retinal inner plexiform layer "absence of the retinal cell layer where bipolar and amacrine cell axons synapse with ganglion cell dendrites" [MGI:monikat "Monika Tomczuk, Mouse Genome Informatics Curator"]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0008823 abnormal ventricular membranous septum morphology "any structural anomaly of the membranous portion of the wall between the two lower chambers of the heart" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

 MP:0008881 absent Harderian gland "absence of the sebaceous gland located behind the eyeball in the orbit that excretes fluid that facilitates movement of the third eyelid" [MESH:A13.445]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarb+,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0008972 ethmoturbinate hypoplasia "underdevelopment or reduced size, usually due to a reduced number of cells, of the conchae of the ethmoid bone which occupy the caudal part of the nasal fossae and form the lateral and superior portions of the turbinate bones in mammals" [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: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0009054 absent anal canal "absence of the terminal portion of the alimentary canal" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0009072 absent cranial vagina "absence of the upper third of the female reproductive canal located between the uterus and the vulva, usually due to a developmental arrest or agenesis of the caudal Mullerian ducts" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0009076 rudimentary Mullerian ducts "not fully developed or remnants of the transient embryonic drainage tubes of the embryonic kidney (mesonephric tubules) that empty into the cloaca and in the female develop into the oviducts, uterus, and cranial vagina" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

 MP:0009438 fusion of cricoid and tracheal cartilages "union of the cricoid cartilage and one or more of the tracheal rings into one structure, when this fusion does not normally occur" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Rarbtm1Ipc/Rarbtm1Ipc,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0009569 abnormal left lung morphology "any structural anomaly of the organ of respiration located on the left side of the body" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

 MP:0009570 abnormal right lung morphology "any structural anomaly of the organ of respiration located on the right side of the body" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

 MP:0009571 abnormal right lung accessory lobe morphology 
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

 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: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 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: Raratm1Ipc/Raratm1Ipc,Rarbtm1Ipc/Rarb+
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

 MP:0010565 absent fetal ductus arteriosus "absence of the fetal vessel that connects the left pulmonary artery with the descending aorta" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Ipc/Rarb+
Genetic Background: involves: 129S2/SvPas

 MP:0010572 persistent right dorsal aorta "persistence of the right dorsal aorta after development; the right dorsal aorta normally regresses but when it persists, a double aortic arch develops; if the left dorsal aorta also regresses, a right aortic arch forms" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Ipc/Rarb+
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

 MP:0010584 abnormal conotruncus septation "anomaly in the process in which the conotruncus separates into the conus cordis, which will give rise to the outflow regions of the ventricles, and the truncus arteriosus which will be divided into proximal ends of the ascending aorta and pulmonary trunk" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0010595 abnormal aortic valve cusp morphology "any structural anomaly of the three fibrous triangular components and associated flap of the aortic valve" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

 MP:0010701 fusion of atlas and odontoid process "the large protuberance that projects upward from the cervical axis (C2), around which the cervical atlas normally rotates, is instead fused to elements of the atlas; the odontoid process may or may not remain attached to the axis" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarb+
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Rara+,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarb+,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rarg+
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0010702 split cervical atlas 
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarb+
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0010703 split cervical axis 
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarb+
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Rara+,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarb+,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rarg+
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0010705 absent metoptic pilar "absence of the posterior border of the optic nerve foramen" [PMID:11493527]
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Allelic Composition: Scn5atm1Clhh/Scn5a+
Genetic Background: involves: 129 * 129S/SvEv * C57BL/6J

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarb+,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarb+,Rargtm1Ipc/Rarg+
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0010706 ventral rotation of lens "a circular shift toward the ventral pole in the position of the equator of the lens relative to the optic nerve exit point" [PMID:7923367]
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Allelic Composition: Aldh1a1tm1.1Ngb/Aldh1a1tm1.1Ngb,Aldh1a3tm1.1Pcn/Aldh1a3tm1.1Pcn
Genetic Background: involves: 129/Sv * C57BL/6 * SJL

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0010707 decreased ventral retina size "decreasd size of the ventral portion of the retina" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", PMID:7923367]
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Allelic Composition: Aldh1a1tm1.1Ngb/Aldh1a1tm1.1Ngb,Aldh1a3tm1.1Pcn/Aldh1a3tm1.1Pcn
Genetic Background: involves: 129/Sv * C57BL/6 * SJL

 MP:0010710 absent sclera "absence of the fibrous, outer envelope of the eyeball, covering it entirely excepting the segment covered anteriorly by the cornea" [MESH:A09.371.784]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0010711 persistent hyperplastic primary vitreous "persistence of the embryonic fibrovascular mesodermal tissue located between the optic cup and lens vesicle that normally regresses during the development of the vitreous body" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Rargtm3.1Ipc/Rargtm3.1Ipc
Genetic Background: involves: C57BL/6 * SJL

Allelic Composition: Rarbtm2Ipc/Rarbtm2Ipc,Rargtm3Ipc/Rargtm3Ipc,H2afvTg(Wnt1-cre)11Rth/?
Genetic Background: involves: 129/Sv * C57BL/6 * SJL

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarb+,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarb+,Rargtm1Ipc/Rarg+
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rarg+
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0010712 absent nasolacrimal duct "absence of the paired channels leading from the lacrimal sacs to the inferior meatus of the nose, through which tears are conducted through the nasal cavity" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0010714 coloboma of the iris "congenital defect of the iris in which some part of the structure is absent" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0010716 coloboma of the optic disc "congenital defect of the optic disc in which some part of the structure is absent" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0010721 short sublingual duct "decreased length of the canals that drain the sublingual gland" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0010722 persistent cervical thymus "the solid lobe of the thymus fails to descend to the mediastinum" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0010728 fusion of atlas and occipital bones "union of elements of the atlas and the bone at the lower, posterior part of the skull into one structure" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarb+,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0010899 abnormal pulmonary alveolar system morphology 
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Allelic Composition: Mapk7tm1Kda/Mapk7tm1Kda
Genetic Background: involves: 129S6/SvEvTac

 MP:0010902 abnormal pulmonary alveolar sac morphology "any structural anomaly of the small terminal dilation of the alveolar ducts around which the alveoli form pocket-like clusters" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Mapk7tm1Kda/Mapk7tm1Kda
Genetic Background: involves: 129S6/SvEvTac

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0010980 ectopic ureteric bud "ureteric bud(s) are not located in the normal or expected position" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

 MP:0010987 abnormal nephrogenic mesenchyme morphogenesis "any structural anomaly of the embryonic connective tissue made up of loosely aggregated mesenchymal cells, supported by interlaminar jelly, in the developing nephron" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

 MP:0010989 fused bronchial cartilage rings "fusion of the hyaline cartilaginous structures that support the bronchi" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Rarbtm1Ipc/Rarbtm1Ipc,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas

 MP:0010995 abnormal lung alveolus development "anomaly in the formation of the sacs for holding air in the lungs, which are formed by the terminal dilation of air passageways" [GO:0048286]
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Allelic Composition: Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * 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: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

 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: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0011290 decreased nephron number "reduction in the total number of filtering units of the kidney" [MGI:anna]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

 MP:0011294 renal glomerulus hypertrophy "increase in the bulk size of the capillary loops of the kidney that normally function as a filtration unit, due to cell enlargement" [MGI:anna]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Ipc/Rarb+
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

 MP:0011407 absent nephrogenic zone "absence of the region found at the periphery of the developing metanephros within which the metanephric mesenchyme aggregates around the tips of the ureteric tree to form the nephrons;in rodents including mice, this region normally persists for a few days postnatally, although it is lost in humans by 36 weeks of gestation" [PMID:17452023]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Ipc/Rarb+
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

 MP:0011486 ectopic ureter "an abnormally placed opening of the ureter, either into the urinary bladder or at another site in the lower urinary or genital tract" [MGI:anna]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 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: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Raratm2Ipc/Raratm2Ipc,Rarbtm1Ipc/Rarbtm1Ipc
Genetic Background: involves: 129S2/SvPas

 MP:0013744 abnormal conjunctival sac morphology "any structural anomaly of the space bound by the conjunctival membrane between the palpebral and bulbar conjunctiva, into which the lacrimal fluid is secreted; it is a closed space when eye is closed; when eye is open, the sac is open anteriorly through the palpebral fissure (between the eyelids)" [http://www.medilexicon.com/medicaldictionary.php?t=79277, MGI:Anna]
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Allelic Composition: Rarbtm2Ipc/Rarbtm2Ipc,Rargtm3Ipc/Rargtm3Ipc,H2afvTg(Wnt1-cre)11Rth/?
Genetic Background: involves: 129/Sv * C57BL/6 * SJL

Allelic Composition: Rarbtm1Mma/Rarbtm1Mma,Rargtm1Ipc/Rargtm1Ipc
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0013826 absent hypoglossal canal "absence of the bony canal in the occipital bone through which the hypoglossal nerve emerges from the skull" [ISBN:0683400088]
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Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

 MP:0030326 decreased periocular mesenchyme apoptosis "reduction in the number of cells of the periocular mesenchyme undergoing programmed cell death" [MGI:anna]
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Allelic Composition: Rarbtm2Ipc/Rarbtm2Ipc,Rargtm3Ipc/Rargtm3Ipc,H2afvTg(Wnt1-cre)11Rth/?
Genetic Background: involves: 129/Sv * C57BL/6 * SJL

 MP:0030406 absent stapes obturator foramen "missing the central foramen (hole) located between the crura and the footplate of the stapes through which the stapedial artery passes" [MGI:anna]
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Allelic Composition: Raratm1Ipc/Raratm1Ipc,Rarbtm1Mma/Rarbtm1Mma
Genetic Background: involves: 129S2/SvPas * C57BL/6

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSMUSG00000004885 Crabp2 / P22935 / Cellular retinoic acid-binding protein 2 / P29373*  / reaction / complex
 ENSMUSG00000039656 Rxrb / P28704 / retinoid X receptor beta / P28702*  / complex
 ENSMUSG00000015846 Rxra / P28700 / retinoid X receptor alpha / P19793*  / complex






 

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