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Gene : CYP4F22 Homo sapiens

Name  ? cytochrome P450 family 4 subfamily F member 22 Cytological Location  19p13.12
Brief Description  cytochrome P450 family 4 subfamily F member 22
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 gene is part of a cluster of cytochrome P450 genes on chromosome 19 and encodes an enzyme thought to play a role in the 12(R)-lipoxygenase pathway. Mutations in this gene are the cause of ichthyosis lamellar type 3. [provided by RefSeq, Jul 2008]
  • synonyms:
  • uc002nbh.5,
  • LI3,
  • NM_173483,
  • CYP4F22,
  • HGNC:26820,
  • OTTHUMG00000182451,
  • FLJ39501,
  • INLNE,
  • cytochrome P450, family 4, subfamily F, polypeptide 22,
  • ARCI5
  • identifiers:
  • 126410,
  • ENSG00000171954,
  • CYP4F22

Genome feature

Region: gene ? Length: 43831  
Location: 19:15508487-15552317 Cyto location: 19p13.12


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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

369 SN Ps

5 Cross References

17 Data Sets

12 Homologues

0 Located Features

97 Rna Seq Results