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Symbol
Name
ID
Acvr2a
activin receptor IIA
MGI:102806
Phenotype annotations related to vision/eye
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
Availability Mouse Genotype
Acvr2atm1.1(KOMP)Vlcg/Acvr2atm1.1(KOMP)Vlcg
Acvr2atm1Hsch/Acvr2atm1Hsch
Acvr2atm1Zuk/Acvr2atm1Zuk

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
04/23/2024
MGI 6.23
The Jackson Laboratory