CYP26B1

Description		cytochrome P450 family 26 subfamily B member 1
Image		No pdb structure
GO Annotations	Cellular Component	Cytoplasm Endoplasmic Reticulum Membrane
	Molecular Function	Retinoic Acid Binding Monooxygenase Activity Iron Ion Binding Protein Binding Retinoic Acid 4-hydroxylase Activity Oxidoreductase Activity 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 Heme Binding
	Biological Process	Cell Fate Determination Establishment Of T Cell Polarity Kidney Development Vitamin Metabolic Process Xenobiotic Metabolic Process Inflammatory Response Male Meiotic Nuclear Division Spermatogenesis Proximal/distal Pattern Formation Positive Regulation Of Gene Expression Sterol Metabolic Process Embryonic Limb Morphogenesis Response To Vitamin A Retinoic Acid Catabolic Process Retinoic Acid Metabolic Process Tongue Morphogenesis Regulation Of T Cell Differentiation Retinoic Acid Receptor Signaling Pathway Negative Regulation Of Retinoic Acid Receptor Signaling Pathway Bone Morphogenesis Establishment Of Skin Barrier Cornification Cellular Response To Retinoic Acid Positive Regulation Of Tongue Muscle Cell Differentiation
Pathways		Vitamins RA biosynthesis pathway Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA)
Drugs		Tretinoin
Diseases
GWAS		Cardiovascular death or myocardial infarction in response to clopidogrel treatment ( 32472697) Heel bone mineral density ( 30598549) Height ( 31562340) IgA levels ( 28628107) Malaria ( 31844061) Schizophrenia ( 25056061)
Novel Interacting Genes		4 novel interacting genes: CEBPG GMCL1 GTF2H2 PCYOX1
Interacting Genes		1 interacting genes: NEDD4L
Entrez ID		56603
HPRD ID		05550
Ensembl ID		ENSG00000003137
Uniprot IDs		E7ER08 Q9NR63
PDB IDs
Enriched GO Terms of Interacting Partners?
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