NR1H3

protein-coding gene in the species Homo sapiens

Facts

13 properties
Instance of
gene
Subclass of
protein-coding gene
Cytogenetic location
11p11.2
Expressed in
right lobe of liver, mucosa of transverse colon, spleen, tibial nerve, subcutaneous adipose tissue, canal of the cervix, gallbladder, lymph node, right lobe of thyroid gland, right adrenal cortex
Found in taxon
Homo sapiens[12]
Genetic association
metabolic disease
Genomic end
47269032, 47290396[6][7]
Genomic start
47248300, 47269851[4][5]
HomoloGene ID
21165[3]
Ortholog
Nr1h3, Nr1h3, nr1h3[8]
Strand orientation
forward strand
🏷️ Also known as
en Liver X receptor alpha en LXR-a en LXRA en NR1H3 en nuclear receptor subfamily 1 group H member 3 en RLD-1

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🔗 Connections
Expressed in 5
Chromosome 1
Found in taxon 1
Genetic association 1
Instance of 1
← Genetic association 1
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Summary

NR1H3 is a gene[1]. NR1H3 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 91. wikidata.org.
  4. [5] ↑ . Ensembl Release 91. wikidata.org.
  5. [6] ↑ . Ensembl Release 91. wikidata.org.
  6. [7] ↑ . Ensembl Release 91. wikidata.org.
  7. [8] ↑ . HomoloGene build68. omabrowser.org. Provenance: wikidata.org.
  8. [9] ↑ . UniProt. Retrieved . wikidata.org.
  9. [10] ↑ . UniProt. Retrieved . wikidata.org.
  10. [11] ↑ . UniProt. Retrieved . wikidata.org.
  11. [12] ↑ . Ensembl Release 91. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). NR1H3. Retrieved November 4, 2026, from https://4ort.xyz/entity/nr1h3
MLA “NR1H3.” 4ort.xyz Knowledge Graph, 4ort.xyz, 4 Nov. 2026, https://4ort.xyz/entity/nr1h3.
BibTeX @misc{4ortxyz_nr1h3_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{NR1H3}}, year = {2026}, url = {https://4ort.xyz/entity/nr1h3}, note = {Accessed: 2026-11-04}}
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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. 24w ago · Mathieu Kappler · 2026-05-20 view diff on Wikidata ↗
    Genetic association → metabolic disease
    Subclass of → —
    Chromosome → human chromosome 11
    Strand orientation → forward strand
    + 8 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-short:0||gsw */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/32527|batch #32527]]: human gene name and description in Alemannic"
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