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Symbol
Name
ID

Tbc1d20
TBC1 domain family, member 20
MGI:1914481

Phenotype annotations related to vision/eye

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
Availability	Mouse Genotype	abnormal eye muscle morphology	abnormal lens morphology	ruptured lens capsule	lens vacuoles	abnormal lens fiber morphology	cataract	developmental cataract	nuclear cataract	small lens	microphthalmia
	Tbc1d20^bs/Tbc1d20^bs
	Tbc1d20^em1Djsi/Tbc1d20^em1Djsi

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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