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Symbol Name ID |
Crb2
crumbs family member 2 MGI:2679260 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hydrocephalus |
Ventriculomegaly |
Gray matter heterotopia |
Seizure |
| Disease(s) Associated with CRB2 | ||||
| ventriculomegaly - cystic kidney disease |
| Mouse Phenotypes | abnormal embryonic neuroepithelium morphology |
open neural tube |
hydrocephaly |
dilated brain ventricle |
abnormal Muller cell morphology |
decreased retina photoreceptor cell number |
abnormal retina bipolar cell morphology |
short retina cone cell outer segment |
short retina rod cell outer segment |
abnormal retina cone cell outer segment morphology |
abnormal retina cone cell morphology |
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| Availability | Mouse Genotype | |||||||||||
| Crb2tm1Vlcg/Crb2tm1Vlcg | ||||||||||||
| Crb2tm1.1Wij/Crb2tm1.1Wij Tg(Chx10-EGFP/cre,-ALPP)2Clc/0 (conditional) |
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| Crb2tm1.1Wij/Crb2tm1.1Wij Tg(Crx-cre)1Tfur/0 (conditional) |
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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 04/23/2024 MGI 6.23 |
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