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Gene : HES7 Homo sapiens

Name  ? hes family bHLH transcription factor 7 Cytological Location  17p13.1
Brief Description  hes family bHLH transcription factor 7
Description  This gene encodes a member of the hairy and enhancer of split family of bHLH transcription factors. The mouse ortholog of this gene is regulated by Notch signaling. The protein functions as a transcriptional repressor, and is implicated in correct patterning of the axial skeleton. A mutation in this gene has been shown to result in spondylocostal dysostosis. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]
  • synonyms:
  • HES7,
  • bHLHb37,
  • HGNC:15977,
  • AB049064,
  • uc002gkc.4,
  • OTTHUMG00000178316,
  • bHLHb37,
  • hairy and enhancer of split 7 (Drosophila),
  • NM_032580,
  • bHLH factor Hes7,
  • SCDO4
  • identifiers:
  • 84667,
  • ENSG00000179111,
  • HES7

Genome feature

Region: gene ? Length: 5443  
Location: 17:8120590-8126032 reverse strand Cyto location: 17p13.1

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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.

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Gene --> Proteins.


Gene Report --> GWAS hit


1 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 --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



0 Pathways

96 SN Ps

5 Cross References

18 Data Sets

17 Homologues

0 Located Features

97 Rna Seq Results