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Symbol
Name
ID
Lca5
Leber congenital amaurosis 5 (human)
MGI:1923032
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Undetectable electroretinogram
Nystagmus
Hypermetropia
High hypermetropia
Visual impairment
Visual loss
Disease(s) Associated with LCA5
Leber congenital amaurosis 5

Mouse Phenotypes
short photoreceptor inner segment
abnormal photoreceptor outer segment morphology
short photoreceptor outer segment
disorganized photoreceptor outer segment
abnormal retinal pigmentation
abnormal retinal photoreceptor layer morphology
abnormal eye physiology
abnormal cone electrophysiology
abnormal rod electrophysiology
Availability Mouse Genotype
Lca5Gt(AG0283)Wtsi/Lca5Gt(AG0283)Wtsi

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
07/29/2020
MGI 6.15
The Jackson Laboratory