PRPH

peripherin

Ensembl:: ENSG00000135406
OMIM:: 170710
Synonyms:: NEF4, PRPH1

Cilia effects upon perturbation of PRPH

Ciliopathy associations

Retinal Dystrophy/Degeneration

Subcellular localization

Ciliary associated gene

Function

Mutations in PRPH cause Retinal Degeneration (PMID: 11853768).

Note: Additional interactive sections (perturbation matrix visualization, phylogenetic conservation strip, protein complex network, STRING interactions) require JavaScript. Browse CiliaHub for the full experience.