|
831
|
|
|
Centrosomal protein 55 |
C10orf3, CT111, MARCH, URCC6 |
|
|
832
|
|
|
CWF19 like cell cycle control factor 1 |
C19L1, SCAR17, hDrn1 |
|
|
833
|
|
|
Coiled-coil domain containing 91 |
HSD8, p56 |
Alzheimer disease, Androgenetic alopecia, Asthma, Attention deficit hyperactivity disorder, Autism, Breast cancer, Breast disease, Cancer, Obstructive pulmonary disease, Colorectal cancer, Dementia, Essential tremor, Estrogen-receptor negative breast cancer, Gastroesophageal reflux disease, Iga nephropathy, Laryngeal disease, Lung cancer, Myopathy, Obesity, Open angle glaucoma, Osteoarthritis, Ovarian cancer, Ovarian serous carcinoma, Parkinson disease, Polycystic ovary syndrome, Prostate cancer, Scoliosis, Seasonal allergic rhinitis, Squamous cell carcinoma, Stroke, Hypertension, Triple-negative breast cancerView all (17 more) |
|
834
|
|
|
Choline dehydrogenase |
- |
|
|
835
|
|
|
Chondroitin sulfate N-acetylgalactosaminyltransferase 2 |
CHGN2, ChGn-2, GALNACT-2, GALNACT2, PRO0082, beta4GalNAcT |
|
|
836
|
|
|
Cell division cycle associated 7 like |
JPO2, R1, RAM2 |
Breast cancer, Ciliary dyskinesia, Color vision deficiency, Connective tissue disease, Melanoma, Dementia, Alzheimer disease, Major depressive disorder, Neurotic disorder, Oligodendroglioma, Situs inversus, Squamous cell carcinoma |
|
837
|
|
|
CDC42 binding protein kinase gamma |
DMPK2, HSMDPKIN, KAPPA-200, MRCKG, MRCKgamma |
|
|
838
|
|
|
Capping protein regulator and myosin 1 linker 1 |
CARMIL, CARMIL1a, LRRC16, LRRC16A, dJ501N12.1, dJ501N12.5 |
Anorexia nervosa, Autism, Bipolar disorder, Color vision deficiency, Coronary artery disease, Crohn disease, Dental caries, Digestive system disease, Gastroesophageal reflux disease, Gout, Heart valve disease, Inflammatory bowel disease, Insomnia, Iron metabolism disorder, Irritable bowel syndrome, Juvenile idiopathic arthritis, Lung cancer, Major depressive disorder, Metabolic syndrome, Kawasaki disease, Neurotic disorder, Obsessive-compulsive disorder, Oligodendroglioma, Psoriasis, Rheumatoid arthritis, Schizophrenia, Hearing loss, Squamous cell carcinoma, Systemic lupus erythematosus, Diabetes mellitus, type 1, Ulcerative colitis, Upper aerodigestive tract neoplasm, Venous thromboembolismView all (18 more) |
|
839
|
|
|
Chromodomain helicase DNA binding protein 7 |
CRG, HH5, IS3, KAL5 |
Angioedema, Atrial septal defect, Atrioventricular septal defect, Attention deficit hyperactivity disorder, Cardiomyopathy, Charge syndrome, Choanal atresia syndrome, Coloboma, Congenital pulmonary artery atresia, Craniofacial ulnar renal syndrome, Developmental disability, Hearing impairment, Hyperopia, Hypogonadotropic hypogonadism, Hypopituitarism, Hypothyroidism, Growth hormone deficiency, Insomnia, Kallmann syndrome, Major depressive disorder, Male infertility spermatogenesis disorder, Myopia, Neurodevelopmental disorders, Omenn syndrome, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature, Pituitary stalk interruption syndrome, Prostate cancer, Prostatic neoplasm, Scoliosis, Sheehan syndrome, Substance abuse, Systemic sclerosis, Wiedemann-steiner syndromeView all (20 more) |
|
840
|
|
|
Cell division cycle 37 like 1, HSP90 cochaperone |
CDC37B, HARC |
|
