| GENE NAME | CYP1A1 |
| CHROMOSOME | 15 |
| ENSEMBL ID | ENSG00000140465 |
| ENTREZ ID | 1543 |
| UNIPROT ACCESSION NUMBER | P04798 |
| GO MOLECULAR FUNCTION | oxygen binding; lyase activity; hydroperoxy icosatetraenoate dehydratase activity; aromatase activity; metal ion binding; monooxygenase activity; oxidoreductase activity |
| ESSENTIAL IN MOUSE | Non-essential |
| PATHWAYS | hsa04913; hsa04913; R-HSA-8978868; R-HSA-2142670; R-HSA-1430728; R-HSA-2142816; R-HSA-9018677; hsa05204; hsa05204; R-HSA-1989781; R-HSA-211859; hsa00380; hsa00380; R-HSA-211897; R-HSA-211945; hsa00140; hsa01100; hsa00140; hsa01100; R-HSA-556833; R-HSA-9018681; hsa00830; hsa00830; R-HSA-211981; R-HSA-2142753; R-HSA-9018678; hsa00980; hsa00980; R-HSA-400206 |
| 4 combinations linked to CYP1A1 | OLI597; OLI348; OLI602; OLI349 |
| 4 variants linked to CYP1A1 | CYP1A1:c.518C>G, p.Thr173Arg; CYP1A1:c.927C>T, p.Asn309=; CYP1A1:c.1162C>G, p.His388Asp; CYP1A1:c.1303C>A, p.Arg435Ser |
| 2 diseases linked to CYP1A1 | Disorder of sex development; 46,XY disorder of sex development |