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RLBP1

protein-coding gene in the species Homo sapiens
Class type of: protein-coding gene Q18031137

Facts

13 properties
Instance of
gene
Subclass of
protein-coding gene
Chromosome
human chromosome 15[12]
Cytogenetic location
15q26.1[17]
Encodes
Retinaldehyde binding protein 1[10]
Expressed in
retinal pigment epithelium, choroid, testicle, caudate nucleus, putamen, right frontal lobe, Brodmann area 9, cingulate gyrus, anterior cingulate cortex, amygdala[18][19][20][21][22][23][24][25][26][27]
Found in taxon
Homo sapiens[11]
Genetic association
Bothnia retinal dystrophy, Newfoundland cone-rod dystrophy, fundus dystrophy[13][14][15]
Genomic end
89764982, 89221614[6][7]
Genomic start
89209869, 89753100[4][5]
HomoloGene ID
68046[3]
Ortholog
Rlbp1, Rlbp1, CG5958[8][9]
Strand orientation
reverse strand[16]
🏷️ Also known as
en CRALBP en retinaldehyde binding protein 1 en RLBP1 ja レチンアルデヒド結合タンパク質1
🔖 Identifiers · 11
Image (Wikimedia Commons)
Protein RLBP1 PDB 1XGG.png ↗
Ensembl gene ID
ENSG00000140522
Ensembl transcript ID
ENST00000567787, ENST00000268125, ENST00000563254, ENST00000564388
Entrez Gene ID
6017
Exact match
identifiers.org
Freebase ID
/m/03gx34y
HGNC ID
10024
HGNC gene symbol
RLBP1
OMIM ID
180090
RefSeq RNA ID
NM_000326, XM_011521870, XM_047432927
UMLS CUI
C1419391

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Summary

RLBP1 is a gene[1]. RLBP1 is a type of protein-coding gene[2].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . Ensembl Release 87. wikidata.org.
  2. [3] ↑ . NCBI Gene. Retrieved . wikidata.org.
  3. [4] ↑ . ensembl Release 106. wikidata.org.
  4. [5] ↑ . ensembl Release 106. wikidata.org.
  5. [6] ↑ . ensembl Release 106. wikidata.org.
  6. [7] ↑ . ensembl Release 106. wikidata.org.
  7. [8] ↑ . HomoloGene build68. omabrowser.org. Provenance: wikidata.org.
  8. [9] ↑ . HomoloGene build68. wikidata.org.
  9. [10] ↑ . UniProt. Retrieved . wikidata.org.
  10. [11] ↑ . ensembl Release 106. wikidata.org.
  11. [12] ↑ . ensembl Release 106. wikidata.org.
  12. [13] ↑ . UniProt. Retrieved . wikidata.org.
  13. [14] ↑ . UniProt. Retrieved . wikidata.org.
  14. [15] ↑ . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  15. [16] ↑ . ensembl Release 106. wikidata.org.
  16. [17] ↑ . NCBI Gene. Retrieved . wikidata.org.
  17. [18] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  18. [19] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  19. [20] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  20. [21] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  21. [22] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  22. [23] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  23. [24] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  24. [25] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  25. [26] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.
  26. [27] ↑ . Bgee. Retrieved . bgee.org. Provenance: wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). RLBP1. Retrieved November 12, 2026, from https://4ort.xyz/entity/rlbp1
MLA “RLBP1.” 4ort.xyz Knowledge Graph, 4ort.xyz, 12 Nov. 2026, https://4ort.xyz/entity/rlbp1.
BibTeX @misc{4ortxyz_rlbp1_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{RLBP1}}, year = {2026}, url = {https://4ort.xyz/entity/rlbp1}, note = {Accessed: 2026-11-12}}
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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 25w ago · Mathieu Kappler · 2026-05-20 view diff on Wikidata ↗
    HGNC gene symbol → RLBP1
    Genetic association → Bothnia retinal dystrophy, Newfoundland cone-rod dystrophy, fundus dystrophy
    RefSeq RNA ID → NM_000326, XM_011521870, XM_047432927
    Exact match → http://identifiers.org/ncbigene/6017
    + 22 other properties edited (see Wikidata diff for full list)
    "Changed [gsw] labels, descriptions or aliases: QuickStatements 3.0 batch #32527: human gene name and description in Alemannic"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.