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Article

RCC1-like domain and ORF15: essentials in RPGR gene.

Advances in experimental medicine and biology - 1 Jan 2006

Jin Zi-Bing, Hayakawa Mutsuko, Murakami Akira, Nao-i Nobuhisa

Abstract excerpt

Clinical research into mutations of the RPGR gene showed that lack of either the RCC1-like domain of the ORF15 causes X-linked retinitis pigmentosa. Thus, the ORF15 and RCC1-like domain play a crucial role in the human retina. Further sudies on the role of the RCC1-like domain in the visual Cascade and additional findings of related proteins in the retina or even other organs, will give us a more precise...

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Source

Identifiers

PMID: 17249551
DOI: 10.1007/0-387-32442-9_5

Genes

RCC1
RPGR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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