|
181
|
|
|
Checkpoint kinase 2 |
CDS1, CHK2, HuCds1, LFS2, PP1425, RAD53, TPDS4, hCds1 |
B lymphoblastic leukemia/lymphoma, Breast adenocarcinoma, Breast cancer, Breast carcinoma, male, Neoplasm of male breast, Mammary neoplasms, Breast carcinoma, Hereditary cancer syndrome, Neoplasm, Carcinoma, Colitis, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Diffuse intrinsic pontine glioma, Diffuse lymphoma, Endometrial carcinoma, Esophagus neoplasm, Fibrofolliculoma, Gastric cancer, Glaucoma, Glioma, Hereditary breast and ovarian cancer syndrome, Hereditary nonpolyposis colorectal cancer, Leiomyosarcoma, Li-fraumeni syndrome, Lung neoplasms, Lung cancer, Lung carcinoma, Lymphoma, Non-hodgkin lymphoma, High grade lymphoma, Intermediate grade lymphoma, Low grade lymphoma, Marfan syndrome, Melanoma, Meningioma, Multiple congenital anomalies, Multiple myeloma, Myeloid leukemia, Nervous system neoplasms, Nephroblastoma, Neuroblastoma, Neuroendocrine tumors, Osteosarcoma, Ovarian neoplasm, Ovarian cancer, Ovarian epithelial carcinoma, Pancreatic neoplasm, Papillary renal carcinoma, Parathyroid adenoma, Peritoneal carcinoma, Polyp of large intestine, Prostate adenocarcinoma, Prostatic neoplasms, Prostate cancer, Prostate cancer, hereditary, Renal carcinoma, Reticulosarcoma, Retinoblastoma, Sarcoma, Skin neoplasms, Stomach neoplasms, Stomach carcinoma, Thymus neoplasms, Thyroid carcinoma, Tumors of adrenal cortexView all (52 more) |
|
182
|
|
|
CHM Rab escort protein |
DXS540, GGTA, HSD-32, REP-1, TCD |
|
|
183
|
|
|
Chimerin 1 |
ARHGAP2, CHN, DURS2, NC, RHOGAP2 |
Aniridia, Arachnodactyly, Blepharophimosis, Blepharospasm, Brachydactyly, Congenital camptodactyly, Congenital clubfoot, Congenital coloboma of iris, Congenital hypoplasia of radius, Dandy-walker syndrome, Developmental delay, Diaphragmatic eventration, Duane retraction syndrome, Duane syndrome, Duane-radial ray syndrome, Dysphagia, Ectopic kidney, Fundus coloboma, Hearing loss, Hydronephrosis, Hypoplasia of optic disc, Laryngomalacia, Microcephaly, Microcornea, Microglossia, Micrognathism, Neck webbing, Nyctalopia, Nystagmus, Oculomotor nerve palsy, Plagiocephaly, Polydactyly, Ptosis, Retinal coloboma, Spina bifida occulta, Stenosis of external auditory canal, Strabismus, UranostaphyloschisisView all (23 more) |
|
184
|
|
|
Chimerin 2 |
ARHGAP3, BCH, CHN2-3, RHOGAP3 |
|
|
185
|
|
|
Calcineurin like EF-hand protein 1 |
CHP, SLC9A1BP, SPAX9, Sid470p, p22, p24 |
|
|
186
|
|
|
CKLF like MARVEL transmembrane domain containing 7 |
CKLFSF7 |
|
|
187
|
|
|
Cholinergic receptor muscarinic 1 |
HM1, M1, M1R |
|
|
188
|
|
|
Cholinergic receptor muscarinic 2 |
HM2 |
Asymmetric diabetic proximal motor neuropathy, Autoimmune diabetes, Bipolar disorder, Diabetes mellitus, Brittle diabetes mellitus, Diabetic amyotrophy, Diabetic asymmetric polyneuropathy, Diabetic autonomic neuropathy, Diabetic mononeuropathy, Diabetic nephropathy, Diabetic neuralgia, Diabetic polyneuropathy, Epilepsy, Esophagus neoplasm, Mental depression, Mood disorder, Neurogenic urinary bladder, Schizophrenia, Symmetric diabetic proximal motor neuropathyView all (4 more) |
|
189
|
|
|
Cholinergic receptor muscarinic 3 |
EGBRS, HM3, PBS, m3AChR |
Abnormal spinal segmentation, Atrial septal defect, Chronic obstructive pulmonary disease, Congenital clubfoot, Developmental dysplasia of the hip, Congenital heart defects, Congenital malrotation of intestine, Congenital pectus carinatum, Congenital pectus excavatum, Congenital posterior urethral valves, Cryptorchidism, Epilepsy, Hydronephrosis, Impaired cognition, Imperforate anus, Intestinal atresia, Intestinal volvulus, Liver cirrhosis, Liver fibrosis, Mental depression, Multicystic renal dysplasia, Patent ductus arteriosus, Prune belly syndrome, Renal insufficiency, Scoliosis, Tetralogy of fallot, Urethral obstruction, Urinary bladder diseases, Uterine anomalies, Ventricular septal defect, Vesicoureteral refluxView all (16 more) |
|
190
|
|
|
Cell division cycle associated 5 |
SORORIN |
|
