Symbol Name ID |
Acvr2a
activin receptor IIA MGI:102806 |
Darker colors indicate more annotations |
Human Phenotypes | Amaurosis fugax |
Visual impairment |
Visual field defect |
Disease(s) Associated with ACVR2A | |||
Lynch syndrome |
Mouse Phenotypes | cyclopia |
microphthalmia |
abnormal eyelid morphology |
anophthalmia |
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Availability | Mouse Genotype | ||||
Acvr2atm1.1(KOMP)Vlcg/Acvr2atm1.1(KOMP)Vlcg | |||||
Acvr2atm1Hsch/Acvr2atm1Hsch | |||||
Acvr2atm1Zuk/Acvr2atm1Zuk |
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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