Symbol Name ID |
Tbc1d20
TBC1 domain family, member 20 MGI:1914481 |
Darker colors indicate more annotations |
Human Phenotypes | Microcornea |
Developmental cataract |
Optic atrophy |
Deeply set eye |
Microphthalmia |
Visual impairment |
Glaucoma |
Ptosis |
Disease(s) Associated with TBC1D20 | ||||||||
Warburg micro syndrome 4 |
Mouse Phenotypes | abnormal eye muscle morphology |
abnormal lens morphology |
ruptured lens capsule |
lens vacuoles |
abnormal lens fiber morphology |
cataract |
developmental cataract |
nuclear cataract |
small lens |
microphthalmia |
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Availability | Mouse Genotype | ||||||||||
Tbc1d20bs/Tbc1d20bs | |||||||||||
Tbc1d20em1Djsi/Tbc1d20em1Djsi |
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 08/02/2024 MGI 6.24 |
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