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Symbol
Name
ID

Alms1
ALMS1, centrosome and basal body associated
MGI:1934606

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Attenuation of retinal blood vessels	Subcapsular cataract	Pigmentary retinopathy	Cone/cone-rod dystrophy	Nystagmus	Photophobia	Visual impairment	Blindness	Constriction of peripheral visual field	Visual loss
Disease(s) Associated with ALMS1
Alstrom syndrome

Mouse Phenotypes		retina photoreceptor degeneration	retina pigment epithelium atrophy	abnormal retina outer nuclear layer morphology	retina outer nuclear layer degeneration	increased susceptibility to age-related retinal degeneration	abnormal eye physiology	abnormal eye electrophysiology
Availability	Mouse Genotype	retina photoreceptor degeneration	retina pigment epithelium atrophy	abnormal retina outer nuclear layer morphology	retina outer nuclear layer degeneration		abnormal eye physiology	abnormal eye electrophysiology
	Alms1^bbb/Alms1^bbb
	Alms1^Gt(XH152)Byg/Alms1^Gt(XH152)Byg
	Alms1^L2131X/Alms1^L2131X
	Alms1^tvrm102/Alms1^tvrm102
	Alms1^tvrm102/Alms1^Gt(XH152)Byg

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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