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Gene : ACOT7 Homo sapiens

Name  ? acyl-CoA thioesterase 7 Cytological Location  1p36.31
Brief Description  acyl-CoA thioesterase 7
Description  This gene encodes a member of the acyl coenzyme family. The encoded protein hydrolyzes the CoA thioester of palmitoyl-CoA and other long-chain fatty acids. Decreased expression of this gene may be associated with mesial temporal lobe epilepsy. Alternatively spliced transcript variants encoding distinct isoforms with different subcellular locations have been characterized. [provided by RefSeq, Jul 2008]
  • synonyms:
  • BACH,
  • ACOT7,
  • OTTHUMG00000001295,
  • BACH,
  • hBACH,
  • LACH1,
  • CTE-II,
  • LACH,
  • CTE-II,
  • brain acyl CoA hydrolase,
  • AB074417,
  • LACH1,
  • MGC1126,
  • uc001ams.4,
  • ACT,
  • NM_007274,
  • ACH1,
  • HGNC:24157,
  • ACT,
  • hBACH,
  • ACH1
  • identifiers:
  • 11332,
  • ENSG00000097021,
  • ACOT7

Genome feature

Region: gene ? Length: 129496  
Location: 1:6264272-6393767 reverse strand Cyto location: 1p36.31

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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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3740 SN Ps

5 Cross References

17 Data Sets

3 Homologues

0 Located Features

97 Rna Seq Results