Rpe65 Phenotype Annotations - Multigenic Genotypes

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Rpe65
retinal pigment epithelium 65
MGI:98001

12 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Cnga3^tm1Biel/Cnga3^tm1Biel Rpe65^tm1Tmr/Rpe65^tm1Tmr involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal eye electrophysiology	J:71529
Lrat^tm1Kpal/Lrat^tm1Kpal Rho^tm1.1Kpal/Rho⁺ Rpe65^450L/Rpe65^450M involves: 129S6/SvEvTac * C57BL/6 * FVB/N	abnormal retina rod cell outer segment morphology	J:170648
	decreased retina photoreceptor cell number	J:170648
	retina degeneration	J:170648
	retina photoreceptor degeneration	J:170648
	retina rod cell degeneration	J:170648
	thin retina outer nuclear layer	J:170648
Plin2^tm1Itl/Plin2^tm1Itl Rpe65^tm1Tmr/Rpe65^tm1Tmr Tyr^c-2J/Tyr^c-2J involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * BALB/c * C57BL/6	abnormal vitamin A metabolism	J:142021
Rho^Tvrm1/Rho⁺ Rpe65^rd12/Rpe65^rd12 B6.Cg-Rpe65^rd12 Rho^Tvrm1	retina outer nuclear layer degeneration	J:159523
	retina photoreceptor degeneration	J:159523
Rho^Tvrm4/Rho⁺ Rpe65^rd12/Rpe65^rd12 B6.Cg-Rpe65^rd12 Rho^Tvrm4	retina outer nuclear layer degeneration	J:159523
	retina photoreceptor degeneration	J:159523
Rpe65^450L/Rpe65^450L Whrn^wi/Whrn^wi 129.Cg(B6)-Whrn^wi	abnormal eye physiology	J:210386
	abnormal retina rod cell inner segment morphology	J:210386
	retina photoreceptor degeneration	J:210386
Rpe65^450M/Rpe65^450M Rpgr^tm1Wbrg/Rpgr^tm1Wbrg involves: 129P2/OlaHsd * BALB/c * C57BL/6	abnormal eye morphology	J:160802
	abnormal eye physiology	J:160802

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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