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Symbol
Name
ID
Crb2
crumbs family member 2
MGI:2679260
Phenotype annotations related to embryo
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
Availability Mouse Genotype
Crb2tm1a(KOMP)Wtsi/Crb2tm1a(KOMP)Wtsi
Crb2tm1Vlcg/Crb2tm1Vlcg

Contributing Projects:
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
The Jackson Laboratory