Pcare Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Pcare
photoreceptor cilium actin regulator
MGI:2385061

19 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Pcare^tm1Kpal/Pcare^tm1Kpal involves: C57BL/6J * C57BL/6NTac	abnormal cone electrophysiology	J:220866
	abnormal electroretinogram waveform feature	J:220866
	abnormal photoreceptor connecting cilium morphology	J:220866
	abnormal photoreceptor inner segment morphology	J:220866
	abnormal retina outer nuclear layer morphology	J:220866
	abnormal retina pigment epithelium morphology	J:220866
	abnormal retina pigmentation	J:220866
	abnormal rod electrophysiology	J:220866
	decreased a-wave amplitude	J:220866
	decreased b-wave amplitude	J:220866
	disorganized photoreceptor outer segment	J:220866
	increased microglial cell activation	J:220866
	photoreceptor outer segment degeneration	J:220866
	retina cone cell degeneration	J:220866
	retina degeneration	J:220866
	retina gliosis	J:220866
	retina outer nuclear layer degeneration	J:220866
	short photoreceptor outer segment	J:220866
	thin retina outer nuclear layer	J:220866

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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