Prom1 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Prom1
prominin 1
MGI:1100886

21 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Prom1^rd19/Prom1^rd19 B6.BXD83-Prom1^rd19/BocJ	abnormal cone electrophysiology	J:215591
	abnormal electroretinogram waveform feature	J:215591
	abnormal eye pigmentation	J:215591
	abnormal retina blood vessel morphology	J:215591
	abnormal retina morphology	J:215591
	abnormal rod electrophysiology	J:215591
	decreased a-wave amplitude	J:215591
	decreased b-wave amplitude	J:215591
	retina degeneration	J:215591
	retina photoreceptor degeneration	J:215591
Prom1^{tm1(cre/ERT2)Gilb}/Prom1^{tm1(cre/ERT2)Gilb} involves: 129S6/SvEvTac	no abnormal phenotype detected	J:144215
Prom1^tm1Pec/Prom1^tm1Pec B6.129-Prom1^tm1Pec	abnormal cone electrophysiology	J:146585
	abnormal retina cone cell morphology	J:146585
	abnormal retina cone cell outer segment morphology	J:146585
	abnormal retina morphology	J:146585
	abnormal retina pigment epithelium morphology	J:146585
	abnormal retina pigmentation	J:146585
	abnormal retina rod cell morphology	J:146585
	abnormal retina rod cell outer segment morphology	J:146585
	abnormal retina vasculature morphology	J:146585
	abnormal rod electrophysiology	J:146585
	photoreceptor outer segment degeneration	J:146585
	retina outer nuclear layer degeneration	J:146585
	retina photoreceptor degeneration	J:146585
	short retina cone cell outer segment	J:146585

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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