Lca5 Phenotype Annotations

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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

Allelic Composition Genetic Background	Annotated Term	Reference
Lca5^{Gt(AG0283)Wtsi}/Lca5^{Gt(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 retina photoreceptor layer morphology	J:174018
	abnormal retina 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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