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Gene : HOXB9 Homo sapiens

Name  ? homeobox B9 Cytological Location  17q21.32
Brief Description  homeobox B9
Description  This gene is a member of the Abd-B 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 leukemia, prostate cancer and lung cancer. [provided by RefSeq, Jul 2008]
  • synonyms:
  • HOX2,
  • NM_024017,
  • HOX2E,
  • HOX2E,
  • HOX2,
  • OTTHUMG00000159907,
  • HOXB9,
  • uc002inx.4,
  • HGNC:5120,
  • HOX-2.5,
  • homeo box B9
  • identifiers:
  • 3219,
  • ENSG00000170689,
  • HOXB9

Genome feature

Region: gene ? Length: 5203  
Location: 17:48621156-48626358 reverse strand Cyto location: 17q21.32


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Function

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

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]

Homology

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Interactions

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Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

387 SN Ps

5 Cross References

15 Data Sets

3 Homologues

0 Located Features

97 Rna Seq Results