SCUBA

CYP19A1 — Cytochrome P450 family 19 subfamily A member 1

CYP19A1 belongs to a gene co-expression module in 1 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.

CYP19A1's module in each cell type

Cell typeModuleShares the module with
MonocytesMulti-lineage Contamination
Cell contamination
AZU1, CLU, E2F2, ELANE, GM2A, GYPC, ITGB7, MS4A3 +4 moreView in SCUBA

About the gene

SynonymsARO, ARO1, aromatase, CPV1, CYAR, CYP19, P-450AROM
Chromosome15: 51208057-51338601
Predicted locationIntracellular, Membrane
Essential geneNo
Protein classCancer-related genes, Disease related genes, Enzymes, FDA approved drug targets, Human disease related genes, Metabolic proteins, Predicted intracellular proteins, Predicted membrane proteins
Molecular functionMonooxygenase, Oxidoreductase
Biological processLipid metabolism

Function

A cytochrome P450 monooxygenase that catalyzes the conversion of C19 androgens, androst-4-ene-3,17-dione (androstenedione) and testosterone to the C18 estrogens, estrone and estradiol, respectively. Catalyzes three successive oxidations of C19 androgens: two conventional oxidations at C19 yielding 19-hydroxy and 19-oxo/19-aldehyde derivatives, followed by a third oxidative aromatization step that involves C1-beta hydrogen abstraction combined with cleavage of the C10-C19 bond to yield a phenolic A ring and formic acid. Alternatively, the third oxidative reaction yields a 19-norsteroid and formic acid. Converts dihydrotestosterone to delta1,10-dehydro 19- nordihydrotestosterone and may play a role in homeostasis of this potent androgen. Also displays 2-hydroxylase activity toward estrone. Mechanistically, uses molecular oxygen inserting one oxygen atom into a substrate, and reducing the second into a water molecule, with two electrons provided by NADPH via cytochrome P450 reductase (CPR; NADPH-ferrihemoprotein reductase).

Human Protein Atlas · Open Targets · UniProt

Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.