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Gene : CYP26C1 Homo sapiens

Name  ? cytochrome P450 family 26 subfamily C member 1 Cytological Location  10q23.33
Brief Description  cytochrome P450 family 26 subfamily C member 1
Description  This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This enzyme is involved in the catabolism of all-trans- and 9-cis-retinoic acid, and thus contributes to the regulation of retinoic acid levels in cells and tissues. This gene is adjacent to a related gene on chromosome 10q23.33. [provided by RefSeq, Jul 2008]
  • synonyms:
  • FFDD4,
  • NM_183374,
  • HGNC:20577,
  • OTTHUMG00000018766,
  • CYP26C1,
  • cytochrome P450, family 26, subfamily C, polypeptide 1,
  • uc010qns.2
  • identifiers:
  • 340665,
  • ENSG00000187553,
  • CYP26C1

Genome feature

Region: gene ? Length: 8743  
Location: 10:93060798-93069540 Cyto location: 10q23.33


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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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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

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

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

Gene Ontology

Gene --> GO terms.

 

Other

3740 SN Ps

4 Cross References

14 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results