501
|
|
|
Cytochrome P450 family 2 subfamily C member 9 |
CPC9, CYP2C, CYP2C10, CYPIIC9, P450-2C9, P450IIC9 |
|
502
|
|
|
Cytochrome P450 family 2 subfamily C member 18 |
CPCI, CYP2C, CYP2C17, P450-6B/29C, P450IIC17 |
|
503
|
|
|
Cytochrome P450 family 2 subfamily D member 7 (gene/pseudogene) |
CYP2D, CYP2D6, CYP2D7AP, CYP2D7P, CYP2D7P1, CYP2D@, P450C2D, P450DB1, RNA40057 |
|
504
|
|
|
Cytochrome P450 family 2 subfamily D member 6 (gene/pseudogene) |
CPD6, CYP2D, CYP2D7AP, CYP2D7BP, CYP2D7P2, CYP2D8P2, CYP2DL1, CYPIID6, P450-DB1, P450C2D, P450DB1 |
Alzheimer disease, Basal ganglia diseases, Breast cancer, Mammary neoplasms, Breast carcinoma, Cryptogenic tonic-clonic epilepsy, Epilepsy, Extrapyramidal disease, Frigidity, Hypoactive sexual desire disorder, Kidney failure, Lenticulostriate disorders, Marfan syndrome, Mental depression, Mood disorder, Neoplasms, Nephritis, Orgasmic disorder, Parkinson disease, Psychosexual disorders, Acute kidney insufficiency, Schizophrenia, Senile dementia, Sexual arousal disorder, Tonic-clonic epilepsyView all (10 more) |
505
|
|
|
Cytochrome P450 family 2 subfamily E member 1 |
CPE1, CYP2E, P450-J, P450C2E |
Adenocarcinoma, Alcoholic fatty liver, Alcoholic liver cirrhosis, Carcinoma, Diffuse lymphoma, Fatty liver, Gout, Gouty arthritis, Lymphoblastic leukemia, Leukemia, Liver neoplasms, Liver cancer, Liver carcinoma, Lung carcinoma, Lung neoplasms, Lung cancer, Lymphoma, Non-hodgkin lymphoma, High grade lymphoma, Intermediate grade lymphoma, Low grade lymphoma, Non-alcoholic fatty liver disease, Obesity, Parkinson disease, Premature ovarian failure, Prostatic neoplasms, Prostate cancer, Reticulosarcoma, Schizophrenia, Spermatogenic failureView all (15 more) |
506
|
|
|
Cell division cycle associated 2 |
PPP1R81, Repo-Man |
|
507
|
|
|
Cytochrome P450 family 3 subfamily A member 4 |
CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4, HLP, NF-25, P450C3, P450PCN1, VDDR3 |
|
508
|
|
|
Cilia and flagella associated protein 418 |
BBS21, C8orf37, CORD16, FAP418, MOT25, RP64, smalltalk |
Anetoderma, Bardet-biedl syndrome, Cataract, Cone-rod dystrophy, Hypoplasia of the ovary, Congenital hypoplasia of penis, Cryptorchidism, Diabetes mellitus, Disorder of eye, Dwarfism, Glaucoma, Hearing loss, Horseshoe kidney, Hyperinsulinism, Hypertension, Hypodontia, Hypogonadism, Keratoconus, Liver fibrosis, Mental retardation, Multicystic renal dysplasia, Myopia, Nephrotic syndrome, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Retinitis pigmentosa, Rod-cone dystrophy, Speech disorders, Syndactyly of fingers, Postaxial hand polydactylyView all (17 more) |
509
|
|
|
Cytochrome P450 family 3 subfamily A member 5 |
CP35, CYPIIIA5, P450PCN3, PCN3 |
|
510
|
|
|
Cytochrome P450 family 3 subfamily A member 51, pseudogene |
CYP3A5-de13c, CYP3A5-de1b2b, CYP3A5P1, CYP3AP1 |
|