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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Lca5
Leber congenital amaurosis 5 (human)
MGI:1923032
10 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Lca5Gt(AG0283)Wtsi/Lca5Gt(AG0283)Wtsi
involves: 129P2/OlaHsd * C57BL/6
abnormal cone electrophysiology J:174018
abnormal eye physiology J:174018
abnormal photoreceptor outer segment morphology J:174018
abnormal retinal photoreceptor layer morphology J:174018
abnormal retinal pigmentation J:174018
abnormal rod electrophysiology J:174018
disorganized photoreceptor outer segment J:174018
normal nervous system phenotype J:174018
short photoreceptor inner segment J:174018
short photoreceptor outer segment J:174018

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