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Gene : HOXD13 Homo sapiens

Name  ? homeobox D13 Cytological Location  2q31.1
Brief Description  homeobox D13
Description  This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located in a cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5' end of this cluster have been associated with severe limb and genital abnormalities. Mutations in this particular gene cause synpolydactyly. [provided by RefSeq, Jul 2008]
  • synonyms:
  • AF005219,
  • homeo box D13,
  • OTTHUMG00000132431,
  • BDSD,
  • uc002ukf.2,
  • HOXD13,
  • SPD1,
  • HOX4I,
  • HGNC:5136,
  • SPD,
  • HOX4I,
  • SPD,
  • BDE,
  • NM_000523,
  • synpolydactyly
  • identifiers:
  • 3239,
  • ENSG00000128714,
  • HOXD13

Genome feature

Region: gene ? Length: 8458  
Location: 2:176087487-176095944 Cyto location: 2q31.1

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


5 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 --> Orthologues


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Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



0 Pathways

327 SN Ps

5 Cross References

17 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results