Symbol Name ID |
Crb2
crumbs family member 2 MGI:2679260 |
Darker colors indicate more annotations |
Human Phenotypes | Polyhydramnios |
Fetal pericardial effusion |
Disease(s) Associated with CRB2 | ||
ventriculomegaly - cystic kidney disease |
Mouse Phenotypes | abnormal vitelline vasculature morphology |
abnormal gastrulation |
failure of initiation of embryo turning |
abnormal endoderm development |
abnormal mesoderm development |
increased embryo size |
abnormal embryonic tissue morphology |
abnormal embryonic epiblast morphology |
abnormal head fold morphology |
abnormal embryonic neuroepithelium morphology |
open neural tube |
abnormal notochord morphology |
abnormal primitive streak morphology |
abnormal anterior primitive streak morphology |
abnormal somite development |
small allantois |
small amniotic cavity |
abnormal chorion morphology |
abnormal placenta morphology |
abnormal visceral yolk sac morphology |
abnormal visceral yolk sac blood island morphology |
abnormal chorioallantoic fusion |
failure of chorioallantoic fusion |
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Availability | Mouse Genotype | |||||||||||||||||||||||
Crb2tm1a(KOMP)Wtsi/Crb2tm1a(KOMP)Wtsi | ||||||||||||||||||||||||
Crb2tm1Vlcg/Crb2tm1Vlcg |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 03/12/2024 MGI 6.23 |
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