CYP4F2 - cytochrome P450 family 4 subfamily F member 2 Gene

Also Known as CPF2

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 8529

About CYP4F2

Cytogenetic location: 19p13.12 Genomic coordinates (GRCh38): 19:15,878,023-15,898,074 (from NCBI)

This gene has 8 transcripts (splice variants), 433 orthologues and 12 paralogues. Biased expression in liver (RPKM 63.5), small intestine (RPKM 42.7) and 2 other tissues.

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. The enzyme starts the process of inactivating and degrading leukotriene B4, a potent mediator of inflammation. This gene is part of a cluster of Cytochrome P450 genes on chromosome 19. Another member of this family, CYP4F11, is approximately 16 kb away. [provided by RefSeq, Jul 2008]

CYP4F2 Products (1)

mRNA Protein Name
NM_001082.5 NP_001073.3 cytochrome P450 4F2 precursor
Molecular Function GO Annotation Evidence References Source
enables alkane 1-monooxygenase activity IDA
IDA: Inferred from direct assay
18433732 GOA
enables alpha-tocopherol omega-hydroxylase activity IDA
IDA: Inferred from direct assay
20861217 GOA
enables arachidonate epoxygenase activity IDA
IDA: Inferred from direct assay
9618440 GOA
enables arachidonate omega-hydroxylase activity IDA
IDA: Inferred from direct assay
9618440 GOA
enables leukotriene-B4 20-monooxygenase activity IDA
IDA: Inferred from direct assay
8026587 GOA
enables long-chain fatty acid omega-hydroxylase activity IDA
IDA: Inferred from direct assay
15145985 GOA
enables oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen IDA
IDA: Inferred from direct assay
19297519 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
17474147 GOA
Biological Process GO Annotation Evidence References Source
involved in arachidonate metabolic process IDA
IDA: Inferred from direct assay
10660572 GOA
involved in epoxygenase P450 pathway IDA
IDA: Inferred from direct assay
9618440 GOA
involved in fatty acid omega-oxidation IDA
IDA: Inferred from direct assay
18577768 GOA
involved in leukotriene B4 catabolic process IDA
IDA: Inferred from direct assay
8026587 GOA
involved in long-chain fatty acid metabolic process IDA
IDA: Inferred from direct assay
18433732 GOA
involved in menaquinone catabolic process IDA
IDA: Inferred from direct assay
24138531 GOA
involved in negative regulation of icosanoid secretion IMP
IMP: Inferred from mutant phenotype
18391101 GOA
involved in omega-hydroxylase P450 pathway IDA
IDA: Inferred from direct assay
9799565 GOA
involved in phylloquinone catabolic process IDA
IDA: Inferred from direct assay
24138531 GOA
involved in positive regulation of icosanoid secretion IMP
IMP: Inferred from mutant phenotype
17341693 GOA
involved in pressure natriuresis IEP
IEP: Inferred from expression pattern
10660572 GOA
involved in regulation of blood pressure IMP
IMP: Inferred from mutant phenotype
18391101 GOA
involved in renal water homeostasis IEP
IEP: Inferred from expression pattern
10660572 GOA
involved in sodium ion homeostasis IEP
IEP: Inferred from expression pattern
10660572 GOA
involved in very long-chain fatty acid metabolic process IDA
IDA: Inferred from direct assay
18433732 GOA
involved in vitamin E metabolic process IDA
IDA: Inferred from direct assay
20861217 GOA
involved in vitamin K catabolic process IDA
IDA: Inferred from direct assay
19297519 GOA
involved in xenobiotic metabolic process IMP
IMP: Inferred from mutant phenotype
21084764 GOA
Cellular Component GO Annotation Evidence References Source
located in apical plasma membrane IDA
IDA: Inferred from direct assay
10660572 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
10660572 GOA
located in intracellular membrane-bounded organelle IDA
IDA: Inferred from direct assay
9618440 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

CYP4F2 Protein Structure

p450

p450: Cytochrome P450 (52 - 506)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 520 a.a.
Protein Preferred Names Protein Names

cytochrome P450 4F2

  • 20-HETE synthase

CYP4F2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
CYP4F2 P78329 UBE2I Homo sapiens Q7KZS0 32296183
Intra
CYP4F2 P78329 UBE2I Homo sapiens Q7KZS0 32296183
Intra
CYP4F2 P78329 UBE2I Homo sapiens Q7KZS0 32296183
Intra
CYP4F2 P78329 RETREG3 Homo sapiens Q86VR2 32296183
Intra
CYP4F2 P78329 RETREG3 Homo sapiens Q86VR2 32296183
Intra
CYP4F2 P78329 RETREG3 Homo sapiens Q86VR2 32296183
Intra
CYP4F2 P78329 JAGN1 Homo sapiens Q8N5M9 32296183
Intra
CYP4F2 P78329 JAGN1 Homo sapiens Q8N5M9 32296183
Intra
CYP4F2 P78329 JAGN1 Homo sapiens Q8N5M9 32296183
Intra
CYP4F2 P78329 PGRMC2 Homo sapiens O15173 32296183
Intra
CYP4F2 P78329 PGRMC2 Homo sapiens O15173 32296183
Intra
CYP4F2 P78329 SPAG4 Homo sapiens Q9NPE6 32296183
Intra
CYP4F2 P78329 SPAG4 Homo sapiens Q9NPE6 32296183
Intra
CYP4F2 P78329 SPAG4 Homo sapiens Q9NPE6 32296183
Intra
CYP4F2 P78329 REEP2 Homo sapiens Q9BRK0 32296183
Intra
CYP4F2 P78329 REEP2 Homo sapiens Q9BRK0 32296183
Intra
CYP4F2 P78329 REEP2 Homo sapiens Q9BRK0 32296183
Intra
CYP4F2 P78329 ZDHHC15 Homo sapiens Q96MV8 32296183
Intra
CYP4F2 P78329 ZDHHC15 Homo sapiens Q96MV8 32296183
Intra
CYP4F2 P78329 ZDHHC15 Homo sapiens Q96MV8 32296183
Intra
CYP4F2 P78329 TLCD4 Homo sapiens Q96MV1 32296183
Intra
CYP4F2 P78329 TLCD4 Homo sapiens Q96MV1 32296183
Intra
CYP4F2 P78329 TLCD4 Homo sapiens Q96MV1 32296183
Intra
CYP4F2 P78329 AQP6 Homo sapiens Q13520 32296183
Intra
CYP4F2 P78329 AQP6 Homo sapiens Q13520 32296183
Intra
CYP4F2 P78329 AQP6 Homo sapiens Q13520 32296183
Intra
CYP4F2 P78329 SCN3B Homo sapiens Q9NY72 32296183
Intra
CYP4F2 P78329 SCN3B Homo sapiens Q9NY72 32296183
Intra
CYP4F2 P78329 SCN3B Homo sapiens Q9NY72 32296183
Intra
CYP4F2 P78329 SLC17A8 Homo sapiens Q8NDX2-2 32296183
Intra
CYP4F2 P78329 SLC17A8 Homo sapiens Q8NDX2-2 32296183
Intra
CYP4F2 P78329 SLC17A8 Homo sapiens Q8NDX2-2 32296183
Intra
CYP4F2 P78329 MUC1 Homo sapiens P15941-11 32296183
Intra
CYP4F2 P78329 MUC1 Homo sapiens P15941-11 32296183
Intra
CYP4F2 P78329 GJA8 Homo sapiens P48165 32296183
Intra
CYP4F2 P78329 GJA8 Homo sapiens P48165 32296183
Intra
CYP4F2 P78329 TSPAN31 Homo sapiens Q12999 32296183
Intra
CYP4F2 P78329 TSPAN31 Homo sapiens Q12999 32296183
Intra
CYP4F2 P78329 TSPAN31 Homo sapiens Q12999 32296183
Intra
CYP4F2 P78329 MMD Homo sapiens Q15546 32296183
Intra
CYP4F2 P78329 MMD Homo sapiens Q15546 32296183
Intra
CYP4F2 P78329 MMD Homo sapiens Q15546 32296183
Intra
CYP4F2 P78329 CPLX4 Homo sapiens Q7Z7G2 32296183
Intra
CYP4F2 P78329 CPLX4 Homo sapiens Q7Z7G2 32296183
Intra
CYP4F2 P78329 CPLX4 Homo sapiens Q7Z7G2 32296183
Intra
CYP4F2 P78329 HSD17B13 Homo sapiens Q7Z5P4 32296183
Intra
CYP4F2 P78329 HSD17B13 Homo sapiens Q7Z5P4 32296183
Intra
CYP4F2 P78329 HSD17B13 Homo sapiens Q7Z5P4 32296183
Intra
CYP4F2 P78329 SLC2A13 Homo sapiens Q96QE2 32296183
Intra
CYP4F2 P78329 SLC2A13 Homo sapiens Q96QE2 32296183
Intra
CYP4F2 P78329 SLC2A13 Homo sapiens Q96QE2 32296183
Intra
CYP4F2 P78329 SLC10A6 Homo sapiens Q3KNW5 32296183
Intra
CYP4F2 P78329 SLC10A6 Homo sapiens Q3KNW5 32296183
Intra
CYP4F2 P78329 SLC10A6 Homo sapiens Q3KNW5 32296183
Intra
CYP4F2 P78329 ELOVL4 Homo sapiens Q9GZR5 32296183
Intra
CYP4F2 P78329 ELOVL4 Homo sapiens Q9GZR5 32296183
Intra
CYP4F2 P78329 ELOVL4 Homo sapiens Q9GZR5 32296183
Intra
CYP4F2 P78329 FAM210B Homo sapiens Q96KR6 32296183
Intra
CYP4F2 P78329 FAM210B Homo sapiens Q96KR6 32296183
Intra
CYP4F2 P78329 FAM210B Homo sapiens Q96KR6 32296183
Intra
CYP4F2 P78329 DNAJC1 Homo sapiens Q96KC8 32296183
Intra
CYP4F2 P78329 DNAJC1 Homo sapiens Q96KC8 32296183
Intra
CYP4F2 P78329 NCK1 Homo sapiens P16333 17474147
Intra
CYP4F2 P78329 EBP Homo sapiens Q15125 32296183
Intra
CYP4F2 P78329 EBP Homo sapiens Q15125 32296183
Intra
CYP4F2 P78329 EBP Homo sapiens Q15125 32296183
Intra
CYP4F2 P78329 MTIF3 Homo sapiens Q9H2K0 32296183
Intra
CYP4F2 P78329 MTIF3 Homo sapiens Q9H2K0 32296183
Intra
CYP4F2 P78329 MTIF3 Homo sapiens Q9H2K0 32296183
Intra
CYP4F2 P78329 SLC19A3 Homo sapiens Q9BZV2 32296183
Intra
CYP4F2 P78329 SLC19A3 Homo sapiens Q9BZV2 32296183
Intra
CYP4F2 P78329 SLC19A3 Homo sapiens Q9BZV2 32296183
Intra
CYP4F2 P78329 CREB3 Homo sapiens O43889-2 25910212
Intra
CYP4F2 P78329 CREB3 Homo sapiens O43889-2 25910212
Intra
CYP4F2 P78329 CREB3 Homo sapiens O43889-2 25910212
Intra
CYP4F2 P78329 TMX2 Homo sapiens Q9Y320 32296183
Intra
CYP4F2 P78329 TMX2 Homo sapiens Q9Y320 32296183
Intra
CYP4F2 P78329 TMX2 Homo sapiens Q9Y320 32296183
Intra
CYP4F2 P78329 TM4SF19 Homo sapiens Q96DZ7 32296183
Intra
CYP4F2 P78329 TM4SF19 Homo sapiens Q96DZ7 32296183
Intra
CYP4F2 P78329 TM4SF19 Homo sapiens Q96DZ7 32296183
Intra
CYP4F2 P78329 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
CYP4F2 P78329 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
CYP4F2 P78329 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
CYP4F2 P78329 SDHAF2 Homo sapiens Q9NX18 32296183
Intra
CYP4F2 P78329 SDHAF2 Homo sapiens Q9NX18 32296183
Intra
CYP4F2 P78329 SDHAF2 Homo sapiens Q9NX18 32296183
Intra
CYP4F2 P78329 TMEM51 Homo sapiens Q9NW97 32296183
Intra
CYP4F2 P78329 TMEM51 Homo sapiens Q9NW97 32296183
Intra
CYP4F2 P78329 TMEM51 Homo sapiens Q9NW97 32296183
Intra
CYP4F2 P78329 THAP4 Homo sapiens Q8WY91 32296183
Intra
CYP4F2 P78329 THAP4 Homo sapiens Q8WY91 32296183
Intra
CYP4F2 P78329 THAP4 Homo sapiens Q8WY91 32296183
Intra
CYP4F2 P78329 LEPROTL1 Homo sapiens O95214 32296183
Intra
CYP4F2 P78329 LEPROTL1 Homo sapiens O95214 32296183
Intra
CYP4F2 P78329 REEP4 Homo sapiens Q9H6H4 32296183
Intra
CYP4F2 P78329 REEP4 Homo sapiens Q9H6H4 32296183
Intra
CYP4F2 P78329 REEP4 Homo sapiens Q9H6H4 32296183
Intra
CYP4F2 P78329 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
CYP4F2 P78329 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
CYP4F2 P78329 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
CYP4F2 P78329 ROM1 Homo sapiens Q03395 32296183
Intra
CYP4F2 P78329 ROM1 Homo sapiens Q03395 32296183
Intra
CYP4F2 P78329 ROM1 Homo sapiens Q03395 32296183
Intra
CYP4F2 P78329 PLEKHO1 Homo sapiens Q53GL0 32296183
Intra
CYP4F2 P78329 PLEKHO1 Homo sapiens Q53GL0 32296183
Intra
CYP4F2 P78329 PLEKHO1 Homo sapiens Q53GL0 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Coumarin Resistance
  • Warfarin Resistance

  • Warfarin Sensitivity

  • Coumadin Sensitivity

  • Warfarin Response

  • Poor Metabolism Of Coumarin

  • Coumarin, Poor Metabolism Of

  • CMRES

Atrial Fibrillation
  • A-Fib

  • Fibrillation, Atrial

  • Af - [Atrial Fibrillation]

  • Rapid Atrial Fibrillation

  • A Fib - [Atrial Fibrillation]

Thrombosis
  • Thrombosis Of Blood Vessel

Inflammatory Bowel Disease 6
  • IBD6

Ichthyosis
  • Ichthyoses

  • Non-Syndromic Ichthyosis

  • Congenital Ichthyosis

Autosomal Recessive Congenital Ichthyosis
  • Lamellar Ichthyosis

  • Congenital Ichthyosiform Erythroderma

  • Li

  • Congenital Nonbullous Ichthyosiform Erythroderma

  • Arci

  • Congenital Lamellar Ichthyosis

  • Nonbullous Congenital Ichthyosiform Erythroderma

  • Cie

  • Congenital Non-Bullous Ichthyosiform Erythroderma

  • Erythrodermic Ichthyosis

  • Nbcie

  • Ncie

  • Non-Bullous Congenital Ichthyosiform Erythroderma

  • Collodion Baby

  • Ichthyosis, Lamellar

  • Non Bullous Congenital Ichthyosiform Erythroderma

  • Ichthyosiform Erythroderma, Brocq Congenital, Nonbullous Form

  • Ichthyosiform Erythroderma, Congenital, Nonbullous, 1

  • Collodion Baby Syndrome

  • Ichthyoses, Lamellar

  • Nbie

  • Nonbullous Ichthyosiform Erythroderma

  • Classic Lamellar Ichthyosis

  • Ichthyosiform Erythroderma Nonbullous Congenital

  • Ichthyosiform Erythroderma Congenital

  • Ichthyosis, Congenital, Autosomal Recessive

  • Ichthyosiform Erythroderma, Congenital

  • Collodion Fetus

  • Non-Bullous Ichthyosiform Erythroderma

Hypertension, Essential
  • Essential Hypertension

  • Hypertension

  • High Blood Pressure

  • Hypertension, Essential, Susceptibility To

  • Hypertensive Disease

  • Primary Hypertension

  • EHT

  • Hypertension, Salt-Sensitive Essential, Susceptibility To

  • Hyperpiesia

  • Idiopathic Hypertension

  • Hypertensive Disorder

  • Hypertension, Essential, Susceptibility To, 3

  • Hypertension, Essential 3

  • Hypertension, Essential, Salt-Sensitive

  • Hypertension, Essential, Susceptibility To, 6

  • Hypertension, Essential 6

  • Hypertension, Salt-Sensitive Essential

  • Hypertension, Susceptibility To

  • Hypertension, Essential, Susceptibility To, 4

  • Hypertension, Essential 4

  • Hypertension, Essential, Susceptibility To, 2

  • Hypertension, Essential 2

  • Hypertension, Essential, Susceptibility To, 1

  • Hypertension, Essential 1

  • Hypertension, Essential, Susceptibility To, 5

  • Hypertension, Essential 5

  • Htn

  • Vascular Hypertensive Disorder

  • Systemic Primary Arterial Hypertension

  • Hbp - [High Blood Pressure]

  • Systemic Arterial Hypertensive Disorder

  • Elevated Blood Pressure

  • Arterial Hypertension Nos

  • Hypertension Nos

  • Benign Hypertension

  • Systemic Arterial Hypertension

  • Systemic Hypertension

  • Artery Htn

  • Benign Htn

  • Vascular Htn

  • Vascular Hypertension

  • Cholesterol Hypertension

  • Cholesterol Htn

  • Idiopathic Htn

  • Malignant Hypertension

  • Malignant Htn

  • Raised Blood Pressure

  • Cardiovascular Hypertension

  • Primary Htn - [Hypertension]

  • High Arterial Tension

  • High Blood Pressure Disorder

  • Ht - [Hypertension]

  • Htn - [Hypertension]

  • Hypertensive Vascular Disease

  • Hypertensive Vascular Degeneration

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Others CYP4F2 NCBI