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Gene · 6101

RP1: RP1 axonemal microtubule associated

12 sourcesgene-search-2026-11-11-0.2.0

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ConductScience Library. RP1: RP1 axonemal microtubule associated. Genes, record 6101. Release gene-search-2026-11-11-0.2.0, 11 Nov 2026. https://conductscience.org/library/genes/6101

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Gene

Symbol
RP1
HGNC
Name
RP1 axonemal microtubule associated
HGNC
NCBI Gene ID
6101
NCBI Gene
HGNC ID
HGNC:10263
HGNC
Ensembl
ENSG00000104237
NCBI Gene
Aliases
DCDC4A, ORP1
NCBI Gene
Type
protein-coding
NCBI Gene

Proteins1

Reviewed human proteins whose Swiss-Prot entry states the gene.

UniProt entryProteinLengthStructuresGene stated in
P56715Oxygen-regulated protein 12,1560Ensembl, GeneID, HGNC

Source UniProt

Patents32

Patents whose sequence listing contains this protein's exact sequence. A patent can list a sequence without claiming it.

PublicationPublishedSEQ ID NOProteinSource
JP 2026515744 A2026-05-19150P56715Espacenet
JP 2026004568 A2026-01-1461460P56715Espacenet
EP 4641201 A22025-10-29338P56715Espacenet
JP 2025517969 A2025-06-12338P56715Espacenet
US 12275959 B22025-04-1535P56715Espacenet
US 12246072 B22025-03-1132P56715Espacenet
WO 2024214081 A12024-10-17150P56715Espacenet
JP 2023551068 A2023-12-06234P56715Espacenet
US 11446398 B22022-09-2072830P56715Espacenet
JP 2022524081 A2022-04-27175801P56715Espacenet

1 to 10 of 32

See all 32 patents

Drugs0

Drugs a ChEMBL mechanism record says act on the gene's protein, through Open Targets.

None in this release.

Trials0

Trials of those drugs. A trial joins the gene only through a drug that acts on it.

None in this release.

NIH grants1,008

NIH grants whose papers are about the gene, through NIH's grant-paper links.

GrantTitleRP1 papersNewest fiscal year
R01EY012910Precision Medicine for Inherited Retinal Degenerations122025
R01EY018213Defining Barriers to Gene Therapy122025
P30CA013696Cancer Center Support Grant92025
ZIAEY000272Inherited Ocular Diseases82025
R01EY024698Gene Editing and Silencing in Phototransduction62025
P30CA016672Cancer Center Support Grant42025
P30EY000331Vision Research Core at UCLA42025
P30EY014801Miami Center for Vision Research42025
R01EY022356Molecular Basis of Human Visual System Disorders42025
P30EY010572Ophthalmology Core Facility32025

1 to 10 of 1,008Source NIH's project files

See all 1,008 nih grants

Papers1,644

Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.

TitleJournalYearPMIDFound bySource
Reversal of repeated red cards reprieves RP-1.Mol Ther Oncol202642701637PubTator, text miningPubMed
Biodistribution, shedding, and transmissibility of vusolimogene oderparepvec (RP1).Front Oncol202642582160PubTator, text miningPubMed
A population-specific genomic reference panel for Taiwan: NHRI-RP-1.J Biomed Sci202642576224PubTator, text miningPubMed
Diagnostic yield and variant spectrum of whole-exome sequencing in Iranian probands with congenital and early-onset ocular disorders.Mol Genet Metab Rep202642495084PubTator, text miningPubMed
Effects of age on the genetic and clinical characteristics of retinitis pigmentosa.Front Ophthalmol (Lausanne)202642434706PubTator, text miningPubMed
Mucinous Cystadenocarcinoma of the Breast: A Clinicopathologic and Molecular Case Report With Literature Review.Int J Surg Pathol202642411451PubTator, text miningPubMed
Inherited retinal disease genes with dual inheritance patterns: insights from the IRD-PT registry.J Med Genet202642321002PubTator, text miningPubMed
Cross-Level Regulatory Interactions Underlying Human Immune Aging.MedComm (2020)202642311858PubTator, text miningPubMed
Genome-wide association study of creatinine clearance identifies new loci for kidney function.Kidney Int202642302930PubTator, text miningPubMed
Expanding the Mutation Spectrum of Non-Syndromic Retinitis Pigmentosa in Consanguineous Pakistani Families: Unraveling Novel Pathogenic Variants in RP1, PDE6B, and PRCD Genes for Precision Diagnosis.Genes (Basel)202642194986PubTator, text miningPubMed

1 to 10 of 1,644

See all 1,644 papers

Sources 12

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • EMBL-EBI's patent proteinsNo added restrictions. Attribution expected
  • GenBank's patent filesNo restrictions from NCBI. Submitters may hold rights
  • HGNCCC0
  • NCBI GenePublic domain (US government)
  • NIH's project files and grant-paper linksPublic domain
  • Open TargetsCC0 1.0
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • EMBL-EBI's patent proteinsEMBL-EBI's patent protein files from the EPO, JPO, KIPO and USPTO. EMBL-EBI: "EMBL-EBI itself places no additional restrictions on the use or redistribution of the data available via its Data Resources and Tools other than those provided by the original data owners" and "EMBL-EBI expects attribution (e.g. in publications, services or products) for the use of any of its Data Resources and Tools." Read on 11 Nov 2026 at https://www.ebi.ac.uk/about/terms-of-use
  • GenBank's patent filesGenBank's patent files. NCBI: "NCBI places no restrictions on the use or distribution of the GenBank data. However, some submitters may claim patent, copyright, or other intellectual property rights in all or a portion of the data they have submitted." Read on 11 Nov 2026 at https://www.ncbi.nlm.nih.gov/genbank/about/
  • HGNCCC0: https://www.genenames.org/about/license/
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH's project files and grant-paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this gene from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/genes/v1/6101

GET https://conductscience.org/api/genes/v1/6101/patents?page=2