3161
|
|
|
Cullin 9 |
H7AP1, PARC |
Syndactyly of the toes, Imperforate anus, Arthritis, Atrial septal defect, Color vision deficiency, Coronary artery disease, Insomnia, Obesity, Peripheral pulmonary artery stenosis, Schizophrenia, Ventricular septal defect |
3162
|
|
|
CutA divalent cation tolerance homolog |
ACHAP, C6orf82 |
|
3163
|
|
|
CutC copper transporter |
CGI-32 |
|
3164
|
|
|
Cut like homeobox 1 |
CASP, CDP, CDP/Cut, CDP1, COY1, CUTL1, CUX, Clox, Cux/CDP, GDDI, GOLIM6, NEDDMS, Nbla10317, p100, p110, p200, p75 |
Alzheimer disease, Androgenetic alopecia, Angioedema, Atrial fibrillation, Attention deficit hyperactivity disorder, Nonsyndromic intellectual disability, Basal cell carcinoma, Breast cancer, Carcinogenesis, Central nervous system cancer, Primary adrenal insufficiency, Duane retraction syndrome, Glucocorticoid deficiency, Glioblastoma, Glioma, Global developmental delay, Intellectual developmental disorder, Keratinocyte carcinoma, Major depressive disorder, Metabolic syndrome, Migraine, Neurodevelopmental disorder, Non-melanoma skin carcinoma, Osteoarthritis, Schizophrenia, Skin cancer, Skin disease, Skin neoplasms, Substance abuse, DepressionView all (15 more) |
3165
|
|
|
Cut like homeobox 2 |
CDP2, CUTL2, DEE67, EIEE67 |
Alzheimer disease, Atrial fibrillation, Bipolar disorder, Breast cancer, Cardiac arrhythmia, Kidney disease, Color vision deficiency, Colorectal cancer, Coronary artery disease, Developmental and epileptic encephalopathy, Epilepsy, Esophageal cancer, Esophageal disease, Gastric cancer, Gastroesophageal reflux disease, Generalized epilepsy, Gout, Hypertension, Osteonecrosis of the femoral head, Kidney failure, Lennox-gastaut syndrome, Major depressive disorder, Myocardial infarction, Partial epilepsy, Polycystic ovary syndrome, Diabetes mellitus type 1, Diabetes mellitus type 2, Venous thromboembolismView all (13 more) |
3166
|
|
|
CUB and zona pellucida like domains 1 |
ERG-1, ERG1, ITMAP1, UO-44 |
|
3167
|
|
|
CWC15 spliceosome associated protein |
AD002, C11orf5, Cwf15, HSPC148, ORF5 |
|
3168
|
|
|
CWC22 spliceosome associated protein |
EIF4GL, NCM, fSAPb |
Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Colorectal cancer, Essential tremor, Female infertility, Gout, Major depressive disorder, Metabolic syndrome, Obesity, Ovarian cancer, Pelvic organ prolapse, Prostate cancer, Schizophrenia, Systemic lupus erythematosus, Diabetes mellitus type 2, Uterine cancerView all (3 more) |
3169
|
|
|
CWC25 spliceosome associated protein |
CCDC49 |
|
3170
|
|
|
CWC27 spliceosome associated cyclophilin |
NY-CO-10, RPSKA, SDCCAG-10, SDCCAG10 |
Brachydactyly-short stature-retinits pigmentosa syndrome, Central nervous system cancer, Color vision deficiency, Diverticular disease, Diverticulitis, Glioblastoma, Glioma, Heart failure, Metaphyseal chondrodysplasia with retinitis pigmentosa, Obesity, Optic atrophy, Osteoarthritis, Osteonecrosis, Retinitis pigmentosa, Retinitis pigmentosa with or without skeletal anomalies, Schizophrenia, Urinary bladder cancerView all (2 more) |
