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CYP2C8 cytochrome P450 family 2 subfamily C member 8 [ Homo sapiens (human) ]

Gene ID: 1558, updated on 2-Nov-2024

Summary

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Official Symbol
CYP2C8provided by HGNC
Official Full Name
cytochrome P450 family 2 subfamily C member 8provided by HGNC
Primary source
HGNC:HGNC:2622
See related
Ensembl:ENSG00000138115 MIM:601129; AllianceGenome:HGNC:2622
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
CPC8; CYPIIC8; CYP2C8DM; MP-12/MP-20
Summary
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 protein localizes to the endoplasmic reticulum and its expression is induced by phenobarbital. The enzyme is known to metabolize many xenobiotics, including the anticonvulsive drug mephenytoin, benzo(a)pyrene, 7-ethyoxycoumarin, and the anti-cancer drug taxol. This gene is located within a cluster of cytochrome P450 genes on chromosome 10q24. Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]
Expression
Restricted expression toward liver (RPKM 350.3) See more
Orthologs
all
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Genomic context

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See CYP2C8 in Genome Data Viewer
Location:
10q23.33
Exon count:
10
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (95036772..95069497, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (95915890..95948616, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (96796529..96829254, complement)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene cytochrome P450 family 2 subfamily C member 59, pseudogene Neighboring gene cytochrome P450 family 2 subfamily C member 60, pseudogene Neighboring gene CYP2C8 promoter Neighboring gene -8 kb enhancer of CYP2C8 Neighboring gene Sharpr-MPRA regulatory region 2936 Neighboring gene uncharacterized LOC107984257 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2637 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2638 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2639 Neighboring gene pro-apoptotic WT1 regulator pseudogene 1 Neighboring gene ReSE screen-validated silencer GRCh37_chr10:96961907-96962201 Neighboring gene acyl-CoA synthetase medium chain family member 6 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:96987152-96987893 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:96988638-96989207

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Expression

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  • Project title: HPA RNA-seq normal tissues HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Bibliography

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Related articles in PubMed

  1. CYP2C8 haplotype structures and their influence on pharmacokinetics of paclitaxel in a Japanese population. Saito Y, et al. Pharmacogenet Genomics, 2007 Jul. PMID 17558302
  2. Impact of the CYP2C8 *3 polymorphism on the drug-drug interaction between gemfibrozil and pioglitazone. Aquilante CL, et al. Br J Clin Pharmacol, 2013 Jan. PMID 22625877, Free PMC Article
  3. Bisphosphonate-related osteonecrosis of the jaw is associated with polymorphisms of the cytochrome P450 CYP2C8 in multiple myeloma: a genome-wide single nucleotide polymorphism analysis. Sarasquete ME, et al. Blood, 2008 Oct 1. PMID 18594024
  4. Functional role of Ile264 in CYP2C8: mutations affect haem incorporation and catalytic activity. Singh R, et al. Drug Metab Pharmacokinet, 2008. PMID 18574320
  5. Association between CYP2C8 (rs1934951) polymorphism and bisphosphonate-related osteonecrosis of the jaws in patients on bisphosphonate therapy: a meta-analysis. Zhong DN, et al. Acta Haematol, 2013. PMID 23171856

See all (240) citations in PubMed

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. The Cytochrome P450 2C8*3 Variant (rs11572080) Is Associated with Improved Asthma Symptom Control in Children and Altered Lipid Mediator Production and Inflammatory Response in Human Bronchial Epithelial Cells.
    Title: The Cytochrome P450 2C8*3 Variant (rs11572080) Is Associated with Improved Asthma Symptom Control in Children and Altered Lipid Mediator Production and Inflammatory Response in Human Bronchial Epithelial Cells.
  2. Potential Association of Cytochrome P450 Copy Number Alteration in Tumour with Chemotherapy Resistance in Lung Adenocarcinoma Patients.
    Title: Potential Association of Cytochrome P450 Copy Number Alteration in Tumour with Chemotherapy Resistance in Lung Adenocarcinoma Patients.
  3. Functional Characterization of Allelic Variations of Human Cytochrome P450 2C8 (V181I, I244V, I331T, and L361F).
    Title: Functional Characterization of Allelic Variations of Human Cytochrome P450 2C8 (V181I, I244V, I331T, and L361F).
  4. CYP2D6 and CYP2C8 pharmacogenetics and pharmacological interactions to predict imatinib plasmatic exposure in GIST patients.
    Title: CYP2D6 and CYP2C8 pharmacogenetics and pharmacological interactions to predict imatinib plasmatic exposure in GIST patients.
  5. CYP2C8 and CYP2J2 gene variations increase the risk of hypertensive intracerebral hemorrhage.
    Title: CYP2C8 and CYP2J2 gene variations increase the risk of hypertensive intracerebral hemorrhage.
  6. [Evaluation of the association of polymorphisms of the CYP2C8 gene with the efficacy and safety of ketorolac in patients with postoperative pain syndrome].
    Title: [Evaluation of the association of polymorphisms of the CYP2C8 gene with the efficacy and safety of ketorolac in patients with postoperative pain syndrome].
  7. The impact of genetic variants in the CYP2C8 gene on bladder cancer susceptibility.
    Title: The impact of genetic variants in the CYP2C8 gene on bladder cancer susceptibility.
  8. The anti-inflammatory role of placental Hofbauer cells is altered in patients with chorioamnionitis: Are CYP2C8 and soluble epoxide hydrolase involved in immunomodulation?
    Title: The anti-inflammatory role of placental Hofbauer cells is altered in patients with chorioamnionitis: Are CYP2C8 and soluble epoxide hydrolase involved in immunomodulation?
  9. Variability of CYP2C8 Polymorphisms in Three Jordanian Populations: Circassians, Chechens and Jordanian-Arabs.
    Title: Variability of CYP2C8 Polymorphisms in Three Jordanian Populations: Circassians, Chechens and Jordanian-Arabs.
  10. The clinically relevant CYP2C8*3 and CYP2C9*2 haplotype is inherited from Neandertals.
    Title: The clinically relevant CYP2C8*3 and CYP2C9*2 haplotype is inherited from Neandertals.
Submit: New GeneRIF Correction See all GeneRIFs (144)

Phenotypes

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Find tests for this gene in the NIH Genetic Testing Registry (GTR)

Review eQTL and phenotype association data in this region using PheGenI

Associated conditions

Description Tests
DRUG METABOLISM, ALTERED, CYP2C8-RELATED
MedGen: C4693948 OMIM: 618018 GeneReviews: Not available
Compare labs
Pioglitazone response
MedGen: CN427422 GeneReviews: Not available
Compare labs
Rosiglitazone response
MedGen: CN427421 GeneReviews: Not available
Compare labs

EBI GWAS Catalog

Description
An atlas of genetic influences on human blood metabolites.
EBI GWAS Catalog
Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy.
EBI GWAS Catalog
Bisphosphonate-related osteonecrosis of the jaw is associated with polymorphisms of the cytochrome P450 CYP2C8 in multiple myeloma: a genome-wide single nucleotide polymorphism analysis.
EBI GWAS Catalog
Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study.
EBI GWAS Catalog
Genome-wide association study of ancestry-specific TB risk in the South African Coloured population.
EBI GWAS Catalog
Genome-wide association study of antibody response to smallpox vaccine.
EBI GWAS Catalog

Variation

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See Variation Viewer (GRCh37.p13)

HIV-1 interactions

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Replication interactions

Interaction Pubs
Knockdown of cytochrome P450, family 2, subfamily C, polypeptide 8 (CYP2C8) by shRNA library screening inhibits HIV-1 replication in cultured Jurkat T-cells PubMed

Go to the HIV-1, Human Interaction Database

Pathways from PubChem

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Interactions

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Products Interactant Other Gene Complex Source Pubs Description

General gene information

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Markers

Homology

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables arachidonate epoxygenase activity IBA
Inferred from Biological aspect of Ancestor
more info
  
enables arachidonate epoxygenase activity IDA
Inferred from Direct Assay
more info
 PubMed 
enables aromatase activity IEA
Inferred from Electronic Annotation
more info
  
enables caffeine oxidase activity IDA
Inferred from Direct Assay
more info
 PubMed 
enables estrogen 16-alpha-hydroxylase activity IDA
Inferred from Direct Assay
more info
 PubMed 
enables heme binding IBA
Inferred from Biological aspect of Ancestor
more info
  
enables iron ion binding IEA
Inferred from Electronic Annotation
more info
  
enables monooxygenase activity IDA
Inferred from Direct Assay
more info
 PubMed 
enables monooxygenase activity TAS
Traceable Author Statement
more info
  
enables oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen IBA
Inferred from Biological aspect of Ancestor
more info
  
enables protein binding IPI
Inferred from Physical Interaction
more info
 PubMed 
enables retinoic acid 4-hydroxylase activity IDA
Inferred from Direct Assay
more info
 PubMed 
Process Evidence Code Pubs
involved_in epoxygenase P450 pathway IBA
Inferred from Biological aspect of Ancestor
more info
  
involved_in epoxygenase P450 pathway IDA
Inferred from Direct Assay
more info
 PubMed 
involved_in epoxygenase P450 pathway TAS
Traceable Author Statement
more info
  
involved_in estrogen metabolic process IDA
Inferred from Direct Assay
more info
 PubMed 
involved_in icosanoid biosynthetic process IDA
Inferred from Direct Assay
more info
 PubMed 
involved_in lipid hydroxylation IDA
Inferred from Direct Assay
more info
 PubMed 
involved_in long-chain fatty acid biosynthetic process TAS
Traceable Author Statement
more info
  
involved_in omega-hydroxylase P450 pathway TAS
Traceable Author Statement
more info
  
involved_in organic acid metabolic process IDA
Inferred from Direct Assay
more info
 PubMed 
involved_in oxidative demethylation IDA
Inferred from Direct Assay
more info
 PubMed 
involved_in retinoic acid metabolic process IDA
Inferred from Direct Assay
more info
 PubMed 
involved_in retinol metabolic process IEA
Inferred from Electronic Annotation
more info
  
involved_in steroid metabolic process IDA
Inferred from Direct Assay
more info
 PubMed 
involved_in xenobiotic catabolic process IDA
Inferred from Direct Assay
more info
 PubMed 
involved_in xenobiotic metabolic process IBA
Inferred from Biological aspect of Ancestor
more info
  
involved_in xenobiotic metabolic process IDA
Inferred from Direct Assay
more info
 PubMed 
involved_in xenobiotic metabolic process TAS
Traceable Author Statement
more info
  
Component Evidence Code Pubs
is_active_in cytoplasm IBA
Inferred from Biological aspect of Ancestor
more info
  
located_in endoplasmic reticulum membrane TAS
Traceable Author Statement
more info
  
is_active_in intracellular membrane-bounded organelle IBA
Inferred from Biological aspect of Ancestor
more info
  
located_in intracellular membrane-bounded organelle IDA
Inferred from Direct Assay
more info
  
located_in plasma membrane IDA
Inferred from Direct Assay
more info
  

General protein information

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Preferred Names
cytochrome P450 2C8
Names
P450 form 1
cytochrome P450 IIC2
cytochrome P450 MP-12
cytochrome P450 MP-20
cytochrome P450 form 1
cytochrome P450, family 2, subfamily C, polypeptide 8
cytochrome P450, subfamily IIC (mephenytoin 4-hydroxylase), polypeptide 8
flavoprotein-linked monooxygenase
microsomal monooxygenase
s-mephenytoin 4-hydroxylase
xenobiotic monooxygenase
NP_000761.3
NP_001185782.1
NP_001185783.1
NP_001185784.1

NCBI Reference Sequences (RefSeq)

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NEW Try the new Transcript table

RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_007972.1 RefSeqGene

    Range
    5001..37726
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. NM_000770.3 → NP_000761.3  cytochrome P450 2C8 isoform a

    See identical proteins and their annotated locations for NP_000761.3

    Status: REVIEWED

    Description
    Transcript Variant: This variant (1) encodes the longest isoform (a).
    Source sequence(s)
    BC020596, M21941, Y00498
    Consensus CDS
    CCDS7438.1
    UniProtKB/Swiss-Prot
    A8K9N8, B0AZN2, B7Z1F6, P10632, Q5VX93, Q8WWB1, Q9UCZ9
    Related
    ENSP00000360317.3, ENST00000371270.6
    Conserved Domains (1) summary
    pfam00067
    Location:30 → 487
    p450; Cytochrome P450

  2. NM_001198853.1 → NP_001185782.1  cytochrome P450 2C8 isoform b

    See identical proteins and their annotated locations for NP_001185782.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (2) differs in the 5' UTR and coding sequence compared to variant 1. The resulting isoform (b) is shorter at the N-terminus compared to isoform a. Variants 2 and 4 both encode the same isoform (b).
    Source sequence(s)
    AK293327, M21941
    Consensus CDS
    CCDS73166.1
    UniProtKB/TrEMBL
    B7Z1F5, B7Z8S1, F5H7Q9
    Related
    ENSP00000485110.1, ENST00000623108.3
    Conserved Domains (1) summary
    pfam00067
    Location:3 → 417
    p450; Cytochrome P450

  3. NM_001198854.1 → NP_001185783.1  cytochrome P450 2C8 isoform c

    See identical proteins and their annotated locations for NP_001185783.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (3) differs in the 5' UTR and coding sequence compared to variant 1. The resulting isoform (c) has a shorter and distinct N-terminus compared to isoform a.
    Source sequence(s)
    AK293327, AK293328, M21941
    Consensus CDS
    CCDS55721.1
    UniProtKB/TrEMBL
    B7Z8S1
    Related
    ENSP00000445062.1, ENST00000535898.5
    Conserved Domains (1) summary
    pfam00067
    Location:5 → 385
    p450; Cytochrome P450

  4. NM_001198855.1 → NP_001185784.1  cytochrome P450 2C8 isoform b

    See identical proteins and their annotated locations for NP_001185784.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (4) differs in the 5' UTR and coding sequence compared to variant 1. The resulting isoform (b) is shorter at the N-terminus compared to isoform a. Variants 2 and 4 both encode the same isoform (b).
    Source sequence(s)
    AK293327, CD014119, M21941
    Consensus CDS
    CCDS73166.1
    UniProtKB/TrEMBL
    B7Z1F5, B7Z8S1, F5H7Q9
    Conserved Domains (1) summary
    pfam00067
    Location:3 → 417
    p450; Cytochrome P450

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    95036772..95069497 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    95915890..95948616 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_030878.1: Suppressed sequence

    Description
    NM_030878.1: This RefSeq was permanently suppressed because it is a nonsense-mediated mRNA decay (NMD) candidate.
Nucleotide Protein
Heading Accession and Version
Protein Accession Links
GenPept Link UniProtKB Link
P10632.2 GenPept UniProtKB/Swiss-Prot:P10632

Gene LinkOut

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Chemical Information
Molecular Biology Databases
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