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Peripherin 2

PRPH2
Identifiers
Aliases PRPH2, AOFMD, AVMD, CACD2, DS, PRPH, RDS, RP7, TSPAN22, rd2, MDBS1, Peripherin 2, peripherin 2 (retinal degeneration, slow)
External IDs MGI: 102791 HomoloGene: 273 GeneCards: PRPH2
Gene location (Human)
Chromosome 6 (human)
Chr. Chromosome 6 (human)
Chromosome 6 (human)
Genomic location for PRPH2
Genomic location for PRPH2
Band 6p21.1 Start 42,696,600 bp
End 42,722,574 bp
RNA expression pattern
PBB GE PRPH2 206625 at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000322

NM_008938

RefSeq (protein)

NP_000313

NP_032964

Location (UCSC) Chr 6: 42.7 – 42.72 Mb Chr 6: 46.91 – 46.92 Mb
PubMed search

NM_000322

NM_008938

NP_000313

NP_032964

Peripherin-2 is a protein, that in humans is encoded by the PRPH2 gene. Peripherin-2 is found in the rod and cone cells of the retina of the eye. Defects in this protein result in one form of retinitis pigmentosa, an incurable blindness.

Mutations in the PRPH2 gene are associated with Vitelliform macular dystrophy.

The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four transmembrane helices. Tetraspanins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility.

Peripherin 2 (sometimes referred to as peripherin/RDS or simply RDS) is a cell surface glycoprotein found in the outer segment of both rod and cone photoreceptor cells. It is located in the rim regions of the flattened disks that contain rhodopsin, which is the protein that is responsible for initiation of visual phototransduction upon reception of light. Peripherin 2 may function as an adhesion molecule involved in stabilization and compaction of outer segment disks or in the maintenance of the curvature of the rim. This protein is essential for disk morphogenesis.


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Wikipedia

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