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Symbol
Name
ID
Tmem231
transmembrane protein 231
MGI:2685024
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Microcornea
Sclerocornea
Cataract
Aplasia/Hypoplasia of the iris
Abnormal chorioretinal morphology
Optic atrophy
Retinopathy
Hypertelorism
Anophthalmia
Microphthalmia
Oculomotor apraxia
Disease(s) Associated with TMEM231
Joubert syndrome 20
Meckel syndrome

Mouse Phenotypes
microphthalmia
Availability Mouse Genotype
Tmem231Gt(OST335874)Lex/Tmem231Gt(OST335874)Lex

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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Funding Information
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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory