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CYP4F12
Gene Name
cytochrome P450, family 4, subfamily F, polypeptide 12
Image
No pdb structure
Gene Ontology Annotations
Cellular Component
Cytoplasm
Endoplasmic Reticulum Membrane
Integral Component Of Membrane
Apical Plasma Membrane
Intracellular Membrane-bounded Organelle
Molecular Function
Iron Ion Binding
Arachidonic Acid Epoxygenase Activity
Alkane 1-monooxygenase Activity
Heme Binding
Vitamin-K-epoxide Reductase (warfarin-sensitive) Activity
Leukotriene-B4 20-monooxygenase Activity
Aromatase Activity
Biological Process
Very Long-chain Fatty Acid Metabolic Process
Long-chain Fatty Acid Metabolic Process
Renal Water Homeostasis
Pressure Natriuresis
Xenobiotic Metabolic Process
Drug Metabolic Process
Arachidonic Acid Metabolic Process
Epoxygenase P450 Pathway
Negative Regulation Of Blood Coagulation
Leukotriene B4 Catabolic Process
Vitamin E Metabolic Process
Vitamin K Biosynthetic Process
Small Molecule Metabolic Process
Sodium Ion Homeostasis
Oxidation-reduction Process
Pathways
Defective CYP2R1 causes Rickets vitamin D-dependent 1B (VDDR1B)
Metabolic disorders of biological oxidation enzymes
Phase 1 - Functionalization of compounds
Defective CYP27B1 causes Rickets vitamin D-dependent 1A (VDDR1A)
Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4)
Defective CYP2U1 causes Spastic paraplegia 56, autosomal recessive (SPG56)
Cytochrome P450 - arranged by substrate type
Biological oxidations
Defective TBXAS1 causes Ghosal hematodiaphyseal dysplasia (GHDD)
Defective FMO3 causes Trimethylaminuria (TMAU)
Defective CYP11A1 causes Adrenal insufficiency, congenital, with 46,XY sex reversal (AICSR)
Defective CYP27A1 causes Cerebrotendinous xanthomatosis (CTX)
Defective CYP11B1 causes Adrenal hyperplasia 4 (AH4)
Eicosanoids
Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA)
Defective CYP1B1 causes Glaucoma
Defective CYP17A1 causes Adrenal hyperplasia 5 (AH5)
Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3)
Defective CYP19A1 causes Aromatase excess syndrome (AEXS)
Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5)
Fatty acids
Defective CYP24A1 causes Hypercalcemia, infantile (HCAI)
Defective MAOA causes Brunner syndrome (BRUNS)
Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency)
Defective CYP21A2 causes Adrenal hyperplasia 3 (AH3)
Drugs
Diseases
GWAS
Protein-protein Interactions
2 interactors:
HSPA6
SOD2
Entrez ID
66002
HPRD ID
07102
Ensembl ID
ENSG00000186204
Uniprot IDs
Q9HCS2
PDB IDs
Enriched GO Terms of Interacting Partners
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Response To Temperature Stimulus
Erythrophore Differentiation
Vasodilation By Acetylcholine Involved In Regulation Of Systemic Arterial Blood Pressure
Age-dependent Response To Reactive Oxygen Species
Response To Magnetism
Response To Silicon Dioxide
Age-dependent Response To Oxidative Stress
Detection Of Oxygen
Response To Selenium Ion
Oxygen Homeostasis
Cellular Response To Ethanol
Hydrogen Peroxide Biosynthetic Process
Response To Isolation Stress
Response To L-ascorbic Acid
Removal Of Superoxide Radicals
Superoxide Anion Generation
Cellular Response To Superoxide
Response To Manganese Ion
Negative Regulation Of Oxidative Stress-induced Intrinsic Apoptotic Signaling Pathway
Protein Refolding
Neurological System Process Involved In Regulation Of Systemic Arterial Blood Pressure
Negative Regulation Of Systemic Arterial Blood Pressure
Response To Superoxide
Intrinsic Apoptotic Signaling Pathway In Response To Oxidative Stress
Response To Immobilization Stress
Response To Oxygen Radical
Regulation Of Oxidative Stress-induced Intrinsic Apoptotic Signaling Pathway
Response To Abiotic Stimulus
Negative Regulation Of Oxidative Stress-induced Cell Death
Release Of Cytochrome C From Mitochondria
Response To Hyperoxia
Regulation Of Mitochondrial Membrane Potential
Vasodilation
Hydrogen Peroxide Metabolic Process
Negative Regulation Of Fibroblast Proliferation
Superoxide Metabolic Process
Positive Regulation Of Nitric Oxide Biosynthetic Process
Positive Regulation Of Reactive Oxygen Species Biosynthetic Process
Response To Electrical Stimulus
Response To Zinc Ion
Negative Regulation Of Blood Pressure
Regulation Of Cellular Response To Oxidative Stress
Cellular Response To Stress
Response To Gamma Radiation
Response To Activity
Response To Cold
Response To Cadmium Ion
Negative Regulation Of Fat Cell Differentiation
Regulation Of Nitric Oxide Biosynthetic Process
Regulation Of Reactive Oxygen Species Biosynthetic Process
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