| GENE NAME | CYP17A1 |
| CHROMOSOME | 10 |
| ENSEMBL ID | None |
| ENTREZ ID | ENSG00000148795 |
| UNIPROT ACCESSION NUMBER | P05093 |
| GO MOLECULAR FUNCTION | ['steroid 17-alpha-monooxygenase activity', 'iron ion binding', 'heme binding', '17-alpha-hydroxyprogesterone aldolase activity', 'oxygen binding'] |
| ESSENTIAL IN MOUSE | Essential |
| PATHWAYS | hsa00140; hsa01100; hsa04913; hsa04917; hsa04927; hsa04934; R-HSA-1430728; R-HSA-1643685; R-HSA-193048; R-HSA-194002; R-HSA-196071; R-HSA-556833; R-HSA-5579028; R-HSA-5579029; R-HSA-5668914; R-HSA-8957322; hsa00140; hsa01100; hsa04913; hsa04917; hsa04927; hsa04934 |
| 1 combination linked to CYP17A1 | OLI1237 |
| 1 variant linked to CYP17A1 | CYP17A1:c.1487G>A, p.Arg496His |
| 1 disease linked to CYP17A1 | Recurrent implantation failure,Primary infertility |