RP1

RP1
Identifiers
Aliases	RP1, DCDC4A, Oretinitis pigmentosa 1 (autosomal dominant), axonemal microtubule associated, RP1 axonemal microtubule associated
External IDs	OMIM: 603937; MGI: 1341105; HomoloGene: 4564; GeneCards: RP1; OMA:RP1 - orthologs
Gene location (Human)
Chr.	Chromosome 8 (human)
End	54,871,720 bp
Gene location (Mouse)
Chr.	Chromosome 1 (mouse)
End	4,479,464 bp
RNA expression pattern
	Top expressed in
	right uterine tube; ; right lung; ; bronchial epithelial cell; ; upper lobe of left lung; ; kidney; ; retina; ; retinal pigment epithelium; ; testicle; ; body of stomach; ; left uterine tube;
	Top expressed in
	retinal pigment epithelium; ; ciliary body; ; spermatocyte; ; spermatid; ; iris; ; morula; ; conjunctival fornix; ; cornea; ; esophagus; ; trachea;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	microtubule binding; protein binding;
Cellular component	cytoplasm; cell projection; photoreceptor outer segment; cilium; microtubule; cytoskeleton; photoreceptor inner segment; microtubule associated complex; axoneme; photoreceptor connecting cilium; ciliary tip;
Biological process	intracellular signal transduction; response to stimulus; photoreceptor cell development; cell projection organization; phototransduction, visible light; visual perception; axoneme assembly; photoreceptor cell outer segment organization; photoreceptor cell maintenance; retinal rod cell development; retinal cone cell development; retina development in camera-type eye; retina morphogenesis in camera-type eye; cellular response to light stimulus; positive regulation of non-motile cilium assembly;
	Sources:Amigo / QuickGO
Orthologs
	6101
	19888
	ENSG00000104237
	ENSMUSG00000025900
	P56715
	P56716
	NM_006269
	NM_001195662; NM_011283; NM_001370921
	NP_006260; NP_001362583
	NP_001182591; NP_035413; NP_001357850
	Wikidata
View/Edit Human	View/Edit Mouse

Oxygen-regulated protein 1 also known as retinitis pigmentosa 1 protein (RP1) is a protein that in humans is encoded by the RP1 gene.^[5]^[6]

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000104237 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000025900 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ Blanton SH, Heckenlively JR, Cottingham AW, Friedman J, Sadler LA, Wagner M, et al. (Mar 1992). "Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8". Genomics. 11 (4): 857–69. doi:10.1016/0888-7543(91)90008-3. PMID 1783394.
^ Cite error: The named reference gene6101 was invoked but never defined (see the help page).

[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000104237 – Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000025900 – Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid1783394-5] Blanton SH, Heckenlively JR, Cottingham AW, Friedman J, Sadler LA, Wagner M, et al. (Mar 1992). "Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8". Genomics. 11 (4): 857–69. doi:10.1016/0888-7543(91)90008-3. PMID 1783394.

[gene6101-6] Cite error: The named reference gene6101 was invoked but never defined (see the help page).

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