RPGR Gene Set

Dataset Pathway Commons Protein-Protein Interactions
Category physical interactions
Type interacting protein
Description retinitis pigmentosa GTPase regulator|This gene encodes a protein with a series of six RCC1-like domains (RLDs), characteristic of the highly conserved guanine nucleotide exchange factors. The encoded protein is found in the Golgi body and interacts with RPGRIP1. This protein localizes to the outer segment of rod photoreceptors and is essential for their viability. Mutations in this gene have been associated with X-linked retinitis pigmentosa (XLRP). Multiple alternatively spliced transcript variants that encode different isoforms of this gene have been reported, but the full-length natures of only some have been determined. [provided by RefSeq, Dec 2008] (NCBI Entrez Gene Database, 6103)
External Link http://www.ncbi.nlm.nih.gov/gene/6103
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Genes

17 interacting proteins for RPGR from the Pathway Commons Protein-Protein Interactions dataset.

Symbol Name
COPS6 COP9 signalosome subunit 6
DCTN1 dynactin 1
DCTN2 dynactin 2 (p50)
IFT88 intraflagellar transport 88
IQCB1 IQ motif containing B1
KIF3A kinesin family member 3A
KIFAP3 kinesin-associated protein 3
NPM1 nucleophosmin (nucleolar phosphoprotein B23, numatrin)
PDE6D phosphodiesterase 6D, cGMP-specific, rod, delta
RHEB Ras homolog enriched in brain
RPGRIP1 retinitis pigmentosa GTPase regulator interacting protein 1
SLC25A10 solute carrier family 25 (mitochondrial carrier; dicarboxylate transporter), member 10
SMC1A structural maintenance of chromosomes 1A
SMC3 structural maintenance of chromosomes 3
TUBG1 tubulin, gamma 1
UBC ubiquitin C
YWHAE tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon