The following gene names and symbols are associated with antigen Retinitis Pigmentosa 1 (Autosomal Dominant) across different species:

retinitis pigmentosa 1 (autosomal dominant) (RP1), retinitis pigmentosa 1 (autosomal dominant) (rp1), retinitis pigmentosa 1 (human) (Rp1)

Other aliases include:

ORP1, DCDC4A, FLJ50293, FLJ55454, FLJ79410, orp1, MGC83581, Rp1h

On the protein level the following designations are being used for antigen Retinitis Pigmentosa 1 (Autosomal Dominant):

retinitis pigmentosa RP1 protein – oxygen-regulated protein 1 – retinitis pigmentosa RP1 protein homolog – retinitis pigmentosa 1 protein – retinitis pigmentosa 1 (autosomal dominant) – rCG30348-like – retinitis pigmentosa 1 homolog – oxygen-regulated protein 1-like

Retinitis Pigmentosa 1 (Autosomal Dominant) is relevant to the following processes:

intracellular signaling cascade – phototransduction, visible light – response to stimulus – visual perception – intracellular signaling pathway

Locations for Retinitis Pigmentosa 1 (Autosomal Dominant):

cilium – soluble fraction

Source: NCBI Entrez Gene, Gene Ontology