CYP21A2 and LCE5A

Data Source:
BioGRID (two hybrid)

		CYP21A2	LCE5A
Description		cytochrome P450 family 21 subfamily A member 2	late cornified envelope 5A
Image			No pdb structure
GO Annotations	Cellular Component	Endoplasmic Reticulum Membrane
	Molecular Function	Steroid 21-monooxygenase Activity Steroid Binding Iron Ion Binding Steroid Hydroxylase Activity Heme Binding 17-hydroxyprogesterone 21-hydroxylase Activity Progesterone 21-hydroxylase Activity	Protein Binding Identical Protein Binding
	Biological Process	Steroid Biosynthetic Process Glucocorticoid Biosynthetic Process Mineralocorticoid Biosynthetic Process Steroid Metabolic Process Sterol Metabolic Process	Keratinization
Pathways		Mineralocorticoid biosynthesis Glucocorticoid biosynthesis Endogenous sterols Defective CYP21A2 causes Adrenal hyperplasia 3 (AH3)	Formation of the cornified envelope
Drugs		Ketoconazole
Diseases		Congenital adrenal hyperplasia (CAH) 46,XX disorders of sex development (Disorders related to androgen excess), including: Congenital adrenal hyperplasias; Glucocorticoid resistance; Aromatase deficiency
GWAS		Asthma ( 31619474) Autism spectrum disorder or schizophrenia ( 28540026) Blood protein levels ( 28240269) Diastolic blood pressure ( 25249183) Diastolic blood pressure x smoking status (current vs non-current) interaction (2df test) ( 29455858) Diastolic blood pressure x smoking status (ever vs never) interaction (2df test) ( 29455858) Hypertension ( 25249183) Inflammatory bowel disease ( 28067908) Postoperative atrial fibrillation in coronary artery bypass grafting surgery ( 26385043) Prostate cancer ( 23535732) Systolic blood pressure ( 25249183) Systolic blood pressure x smoking status (current vs non-current) interaction (2df test) ( 29455858) Systolic blood pressure x smoking status (ever vs never) interaction (2df test) ( 29455858) Ulcerative colitis ( 28067908)	Allergic disease (asthma, hay fever or eczema) ( 29785011) Asthma ( 31619474) Asthma or allergic disease (pleiotropy) ( 29785011) Atopic march ( 26542096) Hair morphology ( 19896111) Inflammatory skin disease ( 25574825)
Interacting Genes		18 interacting genes: CRCT1 CREB5 CYSRT1 HOXA1 KRTAP1-3 KRTAP4-2 KRTAP9-2 LCE1F LCE2C LCE3B LCE3C LCE5A NBPF19 NOTCH2NLA NR4A3 PICK1 POTEB3 POU4F2	66 interacting genes: ADAM12 ALPP CHIC2 CHRD CREB5 CYP21A2 CYSRT1 FBLN1 HOXA1 KRTAP1-1 KRTAP1-3 KRTAP1-5 KRTAP10-1 KRTAP10-5 KRTAP10-7 KRTAP10-8 KRTAP10-9 KRTAP12-3 KRTAP12-4 KRTAP21-2 KRTAP3-1 KRTAP4-1 KRTAP4-11 KRTAP4-12 KRTAP4-2 KRTAP4-4 KRTAP4-5 KRTAP5-11 KRTAP5-2 KRTAP5-3 KRTAP5-4 KRTAP5-6 KRTAP5-9 KRTAP6-2 KRTAP6-3 KRTAP9-2 KRTAP9-3 LCE1A LCE1B LCE1C LCE1E LCE1F LCE2B LCE2C LCE4A NBPF19 NECTIN2 NOTCH2NLA NTAQ1 NUTF2 PLAC8 PLSCR2 PLSCR3 PLSCR4 POU4F2 RGS17 RGS20 RNF4 SLC39A7 SMCP SPRED2 SPRY1 TRIM42 UBE2I VWC2L ZNF655
Entrez ID		1589	254910
HPRD ID		01942	17265
Ensembl ID		ENSG00000231852	ENSG00000186207
Uniprot IDs		P08686 Q08AG9 Q16874	Q5TCM9
PDB IDs		2GEG 4Y8W 5VBU
Enriched GO Terms of Interacting Partners?
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