|
271
|
|
|
Stabilin 1 |
CLEVER-1, FEEL-1, FEEL1, FELE-1, FEX1, HRFT, SCARH2, STAB-1 |
Juvenile arthritis, Bipolar disorder, Kidney disease, Gout, Hodgkin lymphoma, Hyperferritinemia, Juvenile idiopathic arthritis, Kidney failure, Major depressive disorder, Nephrolithiasis, Neurotic disorder, Oligoarticular juvenile idiopathic arthritis |
|
272
|
|
|
Solute carrier family 35 member D1 |
SHNKND, UGTREL7 |
|
|
273
|
|
|
Septin 8 |
SEP2, SEPT8, Septin-8 |
|
|
274
|
|
|
Synaptotagmin 11 |
SYT12, sytXI |
|
|
275
|
|
|
Sulfatase 1 |
SULF-1 |
|
|
276
|
|
|
Spectrin repeat containing nuclear envelope protein 2 |
EDMD5, KASH2, NUA, NUANCE, Nesp2, Nesprin-2, SYNE-2, TROPH |
Anorexia nervosa, Atrial fibrillation, Atrial flutter, Attention deficit hyperactivity disorder, Autism, Emery-dreifuss muscular dystrophy, Bipolar disorder, Renal cell carcinoma, Cardiac arrhythmia, Cardioembolic stroke, Cardiomyopathy, Cerebral palsy, Melanoma, Left ventricular disease, Long qt syndrome, Major depressive disorder, Obsessive-compulsive disorder, Prostate cancer, Psoriasis, Restrictive cardiomyopathy, Schizophrenia, Spastic ataxia, Tourette syndromeView all (8 more) |
|
277
|
|
|
Salt inducible kinase 2 |
LOH11CR1I, QIK, SIK-2, SNF1LK2 |
|
|
278
|
|
|
Sec1 family domain containing 1 |
C14orf163, RA410, SLY1, SLY1P, STXBP1L2 |
|
|
279
|
|
|
SMG6 nonsense mediated mRNA decay factor |
C17orf31, EST1A, SMG-6, hEST1A, hSMG5/7a |
Androgenetic alopecia, Atrial fibrillation, Attention deficit hyperactivity disorder, Bone fracture, Breast cancer, Obstructive pulmonary disease, Coronary artery disease, Diverticular disease, Esophageal cancer, Gastroesophageal reflux disease, Glaucoma, Heart failure, Hypertension, Irritable bowel syndrome, Metabolic syndrome, Migraine, Mitral valve prolapse, Multiple sclerosis, Myocardial infarction, Nonalcoholic fatty liver disease, Obesity, Open angle glaucoma, Osteoarthritis, Schizophrenia, Squamous cell carcinoma, Substance abuse, Diabetes mellitus, type 2, Venous thromboembolismView all (13 more) |
|
280
|
|
|
SATB homeobox 2 |
C2DELq32q33, DEL2Q32Q33, GLSS |
Autism, Cancer, Cerebellar ataxia, Chromosome 2q32-q33 deletion syndrome, Colorectal cancer, Colorectal neoplasm, Craniofacial abnormalities, Desbuquois syndrome, Developmental disability, Dyslexia, Gastroesophageal reflux disease, Glass syndrome, Global developmental delay, Intellectual developmental disorder, Micrognathism, Neurodevelopmental disorders, Oropharyngeal cancer, Satb2 associated syndrome, Schizophrenia, Small cell lung carcinoma, Ulcerative colitis, Uranostaphyloschisis, Uterine fibroidView all (8 more) |