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HOXD@ homeobox D cluster [ Homo sapiens (human) ]

Gene ID: 3230, updated on 17-Aug-2024

Summary

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Official Symbol
HOXD@provided by HGNC
Official Full Name
homeobox D clusterprovided by HGNC
Primary source
HGNC:HGNC:5131
Gene type
other
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
HOX4@
Annotation information
not in current annotation release
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Genomic context

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Location:
2q31.1

Bibliography

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Related articles in PubMed

  1. A mesomelic skeletal dysplasia, Kantaputra-like, not related to HOXD cluster region, and with phenotypic gender differences. Lacarrubba-Flores MDJ, et al. Am J Med Genet A, 2024 Feb. PMID 37846940
  2. Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfoot. Ester AR, et al. Am J Med Genet A, 2009 Dec. PMID 19938081, Free PMC Article
  3. Nomenclature for human homeobox genes. McAlpine PJ, et al. Genomics, 1990 Jul. PMID 1973146
  4. Vertebrate homeobox gene nomenclature. Scott MP. Cell, 1992 Nov 13. PMID 1358459
  5. A common variant in DRD3 receptor is associated with autism spectrum disorder. de Krom M, et al. Biol Psychiatry, 2009 Apr 1. PMID 19058789

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. A mesomelic skeletal dysplasia, Kantaputra-like, not related to HOXD cluster region, and with phenotypic gender differences.
    Title: A mesomelic skeletal dysplasia, Kantaputra-like, not related to HOXD cluster region, and with phenotypic gender differences.
  2. Gene-gene interactions were identified between variants in HOXA, HOXD, and IGFBP3 and with previously associated single nucleotide polymorphisms in mitochondrial-mediated apoptotic genes.
    Title: Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfoot.
  3. Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator)
    Title: Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfoot.
  4. Observational study of gene-disease association. (HuGE Navigator)
    Title: A common variant in DRD3 receptor is associated with autism spectrum disorder.
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General gene information

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Other Names

  • homeo box D cluster
Nucleotide Protein
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