Rp2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Rp2
retinitis pigmentosa 2 homolog
MGI:1277953

14 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Rp2^{Gt(EUCJ0183f04)Hmgu}/Y involves: C57BL/6 * C57BL/6N	abnormal electroretinogram waveform feature	J:219642
	abnormal vision	J:219642
	decreased a-wave amplitude	J:219642
	decreased b-wave amplitude	J:219642
	increased susceptibility to age-related retinal degeneration	J:219642
Rp2^{Gt(EUCJ0183f04)Hmgu}/Rp2^{Gt(EUCJ0183f04)Hmgu} involves: C57BL/6 * C57BL/6N	abnormal b-wave amplitude	J:219642
	abnormal electroretinogram waveform feature	J:219642
	abnormal eye physiology	J:219642
	abnormal vision	J:219642
	decreased a-wave amplitude	J:219642
	decreased b-wave amplitude	J:219642
	increased susceptibility to age-related retinal degeneration	J:219642
Rp2^tm1.1Asw/Rp2^tm1.1Asw involves: 129S/SvEv	normal vision/eye phenotype	J:214194
Rp2^tm1.2Asw/Y involves: 129S/SvEv * C57BL/6	abnormal cone electrophysiology	J:214194
	abnormal retina photoreceptor morphology	J:214194
	abnormal rod electrophysiology	J:214194
	decreased a-wave amplitude	J:214194
	decreased b-wave amplitude	J:214194
	decreased retina cone cell number	J:214194
	disorganized photoreceptor outer segment	J:214194
	thin retina outer nuclear layer	J:214194
	normal vision/eye phenotype	J:214194
Rp2^tm1.2Asw/Rp2^tm1.2Asw involves: 129S/SvEv * C57BL/6	abnormal cone electrophysiology	J:214194
	abnormal retina photoreceptor morphology	J:214194
	abnormal rod electrophysiology	J:214194
	decreased a-wave amplitude	J:214194
	decreased b-wave amplitude	J:214194
	decreased retina cone cell number	J:214194
	disorganized photoreceptor outer segment	J:214194
	thin retina outer nuclear layer	J:214194
	normal vision/eye phenotype	J:214194

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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