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Gene : HOXB7 Homo sapiens

Name  ? homeobox B7 Cytological Location  17q21.32
Brief Description  homeobox B7
Description  This gene is a member of the Antp homeobox family and encodes a protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox B genes located on chromosome 17. The encoded nuclear protein functions as a sequence-specific transcription factor that is involved in cell proliferation and differentiation. Increased expression of this gene is associated with some cases of melanoma and ovarian carcinoma. [provided by RefSeq, Jul 2008]
  • synonyms:
  • homeo box B7,
  • uc002inv.4,
  • HGNC:5118,
  • HOX2,
  • HHO.C1,
  • Hox-2.3,
  • HOX2C,
  • HOX2,
  • OTTHUMG00000170231,
  • HOX2C,
  • NM_004502,
  • HOXB7
  • identifiers:
  • 3217,
  • ENSG00000260027,
  • HOXB7

Genome feature

Region: gene ? Length: 3786  
Location: 17:48607232-48611017 reverse strand Cyto location: 17q21.32

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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


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.



0 Pathways

250 SN Ps

5 Cross References

15 Data Sets

8 Homologues

0 Located Features

97 Rna Seq Results