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Gene : BHLHE22 Homo sapiens

Name  ? basic helix-loop-helix family member e22 Cytological Location  8q12.3
Brief Description  basic helix-loop-helix family member e22
Description  This gene encodes a protein that belongs to the basic helix-loop-helix (bHLH) family of transcription factors that regulate cell fate determination, proliferation, and differentiation. A similar protein in mouse is required for the development of the dorsal cochlear nuclei, and is thought to play a role in in the differentiation of neurons involved in sensory input. The mouse protein also functions in retinogenesis. [provided by RefSeq, Oct 2016]
  • synonyms:
  • basic helix-loop-helix domain containing, class B, 5,
  • trinucleotide repeat containing 20,
  • Beta3,
  • TNRC20,
  • CAGL85,
  • Beta3,
  • BHLHE22,
  • basic helix-loop-helix family, member e22,
  • TNRC20,
  • Beta3a,
  • BHLHB5,
  • NM_152414,
  • U80755,
  • uc003xvi.4,
  • HGNC:11963,
  • BHLHB5,
  • CAGL85,
  • OTTHUMG00000164386
  • identifiers:
  • 27319,
  • ENSG00000180828,
  • BHLHE22

Genome feature

Region: gene ? Length: 3263  
Location: 8:64580365-64583627 Cyto location: 8q12.3

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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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]


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

Gene Ontology

Gene --> GO terms.



0 Pathways

362 SNPs

4 Cross References

13 Data Sets

7 Homologues

0 Located Features

97 Rna Seq Results