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RP1

Retinitis Pigmentosa 1 (autosomal Dominant)

RP1 is a member of the doublecortin family. The protein encoded by this gene contains two doublecortin domains, which bind microtubules and regulate microtubule polymerization. The encoded protein is a photoreceptor microtubule-associated protein and is required for correct stacking of outer segment disc. This protein and the RP1L1 protein, another retinal-specific protein, play essential and synergistic roles in affecting photosensitivity and outer segment morphogenesis of rod photoreceptors. Because of its response to in vivo retinal oxygen levels, this protein was initially named ORP1 (oxygen-regulated protein-1). This protein was subsequently designated RP1 (retinitis pigmentosa 1) when it was found that mutations in this gene cause autosomal dominant retinitis pigmentosa. Mutations in this gene also cause autosomal recessive retinitis pigmentosa. Transcript variants resulted from an alternative promoter and alternative splicings have been found, which overlap the current reference sequence and has several exons upstream and downstream of the current reference sequence. However, the biological validity and full-length nature of some variants cannot be determined at this time.

Gene Name: Retinitis Pigmentosa 1 (autosomal Dominant)
Synonyms: RP1, ORP1, Oxygen-regulated protein 1, Retinitis pigmentosa 1, Retinitis pigmentosa 1 protein, DCDC4A
Target Sequences: NM_006269 NP_006260.1 P56715

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RP1 Antibody - Immunohistochemistry: RP1 Antibody - IHC analysis of RP1 in mouse retina.
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RP1 Rabbit anti-Human Polyclonal (aa2000-2156) Antibody
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PLEASE NOTE

For RESEARCH USE ONLY. Intended for use by laboratory professionals. Not intended for human diagnostic or therapeutic purposes.

The data on this page has been compiled from LifeSpan internal sources, the National Center for Biotechnology Information (NCBI), and The Universal Protein Resource (UniProt).