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  2. CYP4A11 - cytochrome P450 family 4 subfamily A member 11 Gene

CYP4A11 - cytochrome P450 family 4 subfamily A member 11 Gene

中文名称:细胞色素 P450 家族 4 亚家族 A 成员 11

种属: Homo sapiens

同用名: CP4Y; CYP4A2; CYP4AII; CYPIVA11

基因 ID: 1579 | 基因类型: protein coding

关于 CYP4A11

Cytogenetic location: 1p33 Genomic coordinates (GRCh38): 1:46,929,188-46,941,476 (from NCBI)

This gene has 8 transcripts (splice variants), 376 orthologues and 12 paralogues. Biased expression in liver (RPKM 280.4) and kidney (RPKM 130.2).

功能概要

该基因编码细胞色素 P450 酶超家族的成员。细胞色素 P450 蛋白是单加氧酶,可催化许多涉及药物代谢和胆固醇、类固醇和其他脂质合成的反应。这种蛋白质定位于内质网并羟基化中链脂肪酸,如月桂酸盐和肉豆蔻酸盐。已发现该基因的多个转录变体。[RefSeq 提供,2016 年 1 月]

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 hydroxylates medium-chain fatty acids such as laurate and myristate. Multiple transcript variants have been found for this gene. [provided by RefSeq, Jan 2016]

CYP4A11 基因产物(3)

mRNA Protein Name
NM_000778.4 NP_000769.2 cytochrome P450 4A11 isoform 1
NM_001319155.2 NP_001306084.1 cytochrome P450 4A11 isoform 2
NM_001363587.2 NP_001350516.1 cytochrome P450 4A11 isoform 3
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables alkane 1-monooxygenase activity IDA
IDA: 通过直接分析推断
18433732 GOA
enables arachidonate epoxygenase activity IDA
IDA: 通过直接分析推断
9618440 GOA
enables leukotriene-B4 20-monooxygenase activity IDA
IDA: 通过直接分析推断
9799565 GOA
enables long-chain fatty acid omega-hydroxylase activity IDA
IDA: 通过直接分析推断
15145985 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in arachidonate metabolic process IDA
IDA: 通过直接分析推断
10660572 GOA
involved in epoxygenase P450 pathway IDA
IDA: 通过直接分析推断
9618440 GOA
involved in leukotriene metabolic process IDA
IDA: 通过直接分析推断
9799565 GOA
involved in long-chain fatty acid metabolic process IDA
IDA: 通过直接分析推断
18433732 GOA
involved in positive regulation of icosanoid secretion IMP
IMP: 通过突变表型推断
18391101 GOA
involved in pressure natriuresis IEP
IEP: 通过表达模式推断
10660572 GOA
involved in renal water homeostasis IEP
IEP: 通过表达模式推断
10660572 GOA
involved in sodium ion homeostasis IEP
IEP: 通过表达模式推断
10660572 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in apical plasma membrane IDA
IDA: 通过直接分析推断
10660572 GOA
located in cytoplasm IDA
IDA: 通过直接分析推断
10660572 GOA
located in intracellular membrane-bounded organelle IDA
IDA: 通过直接分析推断
9618440 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

CYP4A11 蛋白结构

p450

p450: Cytochrome P450 (52 - 502)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 519 a.a.
蛋白主名 其他名称

cytochrome P450 4A11

20-HETE synthase

CYP4A11 抗体

目录号 产品名 应用 反应物种
HY-P82342 Cytochrome P450 4A/CYP4A11 Antibody (YA2087) WB, IHC-P, IP Human, Mouse, Rat

关联疾病

疾病名称 别名
Peroxisomal Acyl-Coa Oxidase Deficiency

Pseudoneonatal Adrenoleukodystrophy

Straight-Chain Acyl-Coa Oxidase Deficiency

Pseudoadrenoleukodystrophy

PSEUDO-NALD

Pseudo-Neonatal Adrenoleukodystrophy

Acyl-Coa Oxidase Deficiency

Peroxisomal Acyl-Coenzyme A Oxidase

Acyl-Coenzyme A Oxidase Deficiency

Adrenoleukodystrophy, Pseudoneonatal

Deficiency, Peroxisomal Acyl-Coa Oxidase

Bietti Crystalline Corneoretinal Dystrophy

BCD

Bietti Crystalline Dystrophy

Bietti Tapetoretinal Degeneration With Marginal Corneal Dystrophy

Bietti Crystalline Retinopathy

Bietti'S Crystalline Dystrophy

Crystalline Retinopathy

Dystrophy, Corneoretinal, Crystalline, Bietti

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

Gliosarcoma

Glioblastoma With Sarcomatous Component

Sarcomatous Glioblastoma

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

疾病名称 别名
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