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Gene : HR Homo sapiens

Name  ? HR lysine demethylase and nuclear receptor corepressor Cytological Location  8p21.3
Brief Description  HR lysine demethylase and nuclear receptor corepressor
Description  This gene encodes a protein that is involved in hair growth. This protein functions as a transcriptional corepressor of multiple nuclear receptors, including thyroid hormone receptor, the retinoic acid receptor-related orphan receptors and the vitamin D receptors, and it interacts with histone deacetylases. The translation of this protein is modulated by a regulatory open reading frame (ORF) that exists upstream of the primary ORF. Mutations in this upstream ORF cause Marie Unna hereditary hypotrichosis (MUHH), an autosomal dominant form of genetic hair loss. Mutations in this gene also cause autosomal recessive congenital alopecia and atrichia with papular lesions, other diseases resulting in hair loss. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2014]
  • synonyms:
  • HYPT4,
  • MUHH1,
  • NM_005144,
  • OTTHUMG00000097089,
  • hairless homolog (mouse),
  • AU,
  • AF039196,
  • ALUNC,
  • HSA277165,
  • HR,
  • uc003xas.4,
  • hair growth associated,
  • HGNC:5172,
  • ALUNC,
  • AU,
  • MUHH
  • identifiers:
  • 55806,
  • ENSG00000168453,
  • HR

Genome feature

Region: gene ? Length: 18966  
Location: 8:22114419-22133384 reverse strand Cyto location: 8p21.3

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Proteins.


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3 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

177 SN Ps

5 Cross References

18 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results