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Gene : EPHX2 Homo sapiens

Name  ? epoxide hydrolase 2 Cytological Location  8p21.2-p21.1
Brief Description  epoxide hydrolase 2
Description  This gene encodes a member of the epoxide hydrolase family. The protein, found in both the cytosol and peroxisomes, binds to specific epoxides and converts them to the corresponding dihydrodiols. Mutations in this gene have been associated with familial hypercholesterolemia. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2012]
  • synonyms:
  • L05779,
  • CEH,
  • ABHD20,
  • HGNC:3402,
  • EPHX2,
  • ABHD20,
  • OTTHUMG00000102115,
  • SEH,
  • epoxide hydrolase 2, cytoplasmic,
  • NM_001979,
  • uc003xfu.5
  • identifiers:
  • 2053,
  • ENSG00000120915,
  • EPHX2

Genome feature

Region: gene ? Length: 106417  
Location: 8:27491143-27597559 Cyto location: 8p21.2-p21.1


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Function

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Proteins

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SNPs

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Disease

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]

Homology

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Interactions

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Expression

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Other

3753 SN Ps

5 Cross References

19 Data Sets

3 Homologues

0 Located Features

97 Rna Seq Results