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Gene : HOXD1 Homo sapiens

Name  ? homeobox D1 Cytological Location  2q31.1
Brief Description  homeobox D1
Description  This gene is a member of the Antp homeobox family and encodes a protein with a homeobox DNA-binding domain. This nuclear protein functions as a sequence-specific transcription factor that is involved in differentiation and limb development. Mutations in this gene have been associated with severe developmental defects on the anterior-posterior (a-p) limb axis. [provided by RefSeq, Jul 2008]
  • synonyms:
  • NM_024501,
  • homeo box D1,
  • HOX4,
  • HOX4G,
  • HGNC:5132,
  • OTTHUMG00000132512,
  • HOX4,
  • uc002ukv.5,
  • HOXD1,
  • HOX4G,
  • Hox-4.7
  • identifiers:
  • 3231,
  • ENSG00000128645,
  • HOXD1

Genome feature

Region: gene ? Length: 2240  
Location: 2:176188668-176190907 Cyto location: 2q31.1

Uni Prot Comments Displayer

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Gene Expression Atlas Diseases Displayer

Publication Counts Displayer

Curated Proteins Displayer


Gene Ontology Displayer

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


0 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


Homologue Displayer


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Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



443 SN Ps

5 Cross References

14 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results