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Gene : BHLHE41 Homo sapiens

Name  ? basic helix-loop-helix family member e41 Cytological Location  12p12.1
Brief Description  basic helix-loop-helix family member e41
Description  This gene encodes a basic helix-loop-helix protein expressed in various tissues. The encoded protein can interact with ARNTL or compete for E-box binding sites in the promoter of PER1 and repress CLOCK/ARNTL's transactivation of PER1. This gene is believed to be involved in the control of circadian rhythm and cell differentiation. Defects in this gene are associated with the short sleep phenotype. [provided by RefSeq, Feb 2014]
  • synonyms:
  • OTTHUMG00000169174,
  • NM_030762,
  • Enhancer-of-split and hairy-related protein 1,
  • DEC2,
  • BHLHB3,
  • SHARP1,
  • differentially expressed in chondrocytes 2,
  • uc001rhb.4,
  • HGNC:16617,
  • basic helix-loop-helix family, member e41,
  • SHARP1,
  • basic helix-loop-helix domain containing, class B, 3,
  • SHARP-1,
  • BHLHE41,
  • BHLHB3,
  • AB044088,
  • DEC2,
  • FNSS1,
  • hDEC2
  • identifiers:
  • 79365,
  • ENSG00000123095,
  • BHLHE41

Genome feature

Region: gene ? Length: 5008  
Location: 12:26120030-26125037 reverse strand Cyto location: 12p12.1

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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 Ontology

Gene --> GO terms.



335 SN Ps

5 Cross References

16 Data Sets

15 Homologues

0 Located Features

97 Rna Seq Results