Rdh13 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Rdh13
retinol dehydrogenase 13 (all-trans and 9-cis)
MGI:1918732

7 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Rdh13^tm1Lex/Rdh13^tm1Lex B6;129S5-Rdh13^tm1Lex/Mmucd	abnormal locomotor coordination	J:171883
Rdh13^tm1Xuxn/Rdh13^tm1Xuxn 129.Cg-Rdh13^tm1Xuxn	abnormal photoreceptor inner segment morphology	J:191615
	abnormal retina photoreceptor layer morphology	J:191615
	abnormal rod electrophysiology	J:191615
	increased susceptibility to injury	J:191615
	retina outer nuclear layer degeneration	J:191615
	thin retina outer nuclear layer	J:191615

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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