Symbol Name ID |
Krit1
KRIT1, ankyrin repeat containing MGI:1930618 |
Darker colors indicate more annotations |
Human Phenotypes | Retinal vascular malformation |
Disease(s) Associated with KRIT1 | |
cerebral cavernous malformation 1 |
Mouse Phenotypes | abnormal retina vasculature morphology |
increased retina hemangioma incidence |
absent optic nerve |
abnormal eye morphology |
abnormal optic vesicle formation |
eye lesions |
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Availability | Mouse Genotype | ||||||
Krit1tm1.1(KOMP)Vlcg/Krit1tm1.1(KOMP)Vlcg | |||||||
Krit1tm1.1(KOMP)Vlcg/Krit1+ | |||||||
Krit1tm1Arte/Krit1tm1Arte Tg(Cdh5-cre/ERT2)1Rha/0 (conditional) |
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Krit1tm1Kwhi/Krit1tm1.1Kwhi Tg(Pdgfb-icre/ERT2,-EGFP)1Frut/0 (conditional) |
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 04/30/2024 MGI 6.23 |
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