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Symbol
Name
ID

Krit1
KRIT1, ankyrin repeat containing
MGI:1930618

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Intracranial hemorrhage	Cerebral cavernous malformation	Cerebral calcification	Headache	Seizure
Disease(s) Associated with KRIT1
cerebral cavernous malformation 1

Mouse Phenotypes		abnormal brain vasculature morphology	abnormal neural tube morphology	abnormal neural tube closure	absent optic nerve
Availability	Mouse Genotype	abnormal brain vasculature morphology	abnormal neural tube morphology	abnormal neural tube closure	absent optic nerve
	Krit1^{tm1.1(KOMP)Vlcg}/Krit1^{tm1.1(KOMP)Vlcg}
	Krit1^{tm1.1(KOMP)Vlcg}/Krit1⁺
	Krit1^tm1Arte/Krit1^tm1Arte Tg(Cdh5-cre/ERT2)1Rha/0 (conditional)
	Krit1^tm1Kwhi/Krit1^tm1Kwhi Tg(Cdh5-cre/ERT2)1Rha/0 (conditional)
	Krit1^tm1Kwhi/Krit1^tm1.1Kwhi Tg(Pdgfb-icre/ERT2,-EGFP)1Frut/0 (conditional)

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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