CYP4F22

Description		cytochrome P450 family 4 subfamily F member 22
Image		No pdb structure
GO Annotations	Cellular Component	Endoplasmic Reticulum Membrane Integral Component Of Membrane
	Molecular Function	Monooxygenase Activity Iron Ion Binding Protein Binding Oxidoreductase Activity, Acting On Paired Donors, With Incorporation Or Reduction Of Molecular Oxygen Heme Binding
	Biological Process	Icosanoid Metabolic Process Ceramide Biosynthetic Process
Pathways		Fatty acids Miscellaneous substrates Eicosanoids Synthesis of Leukotrienes (LT) and Eoxins (EX) Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5)
Drugs
Diseases		Lamellar ichthyosis (LI) and Non-bullous congenital ichthyosiform erythroderma (NBCIE)
GWAS		Lymphocyte counts ( 32888494) Monocyte count ( 32888494)
Interacting Genes		4 interacting genes: AQP6 MSMO1 REEP2 TLCD4
Entrez ID		126410
HPRD ID		08256
Ensembl ID		ENSG00000171954
Uniprot IDs		Q6NT55
PDB IDs
Enriched GO Terms of Interacting Partners?
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