|
291
|
|
|
Sirtuin 1 |
SIR2, SIR2L1, SIR2alpha |
Atherosclerosis, Atrial fibrillation, Autoimmune diseases, Bipolar disorder, Brain neoplasms, Brain infarction, Breast cancer, Mammary neoplasms, Breast carcinoma, Intracranial neoplasm, Cirrhosis, Colitis, Congestive heart failure, Degenerative diseases, central nervous system, Demyelinating diseases, Diabetes mellitus, Diabetic retinopathy, Fatty liver, Heart diseases, Heart failure, Kidney failure, Marfan syndrome, Metabolic syndrome, Mood disorder, Myocardial infarction, Neurodegenerative disorders, Neuronal ceroid lipofuscinosis, Non-alcoholic fatty liver disease, Obesity, Osteosarcoma, Paroxysmal atrial fibrillation, Prostatic neoplasms, Prostate cancer, Acute kidney insufficiency, Retinal diseases, Schizophrenia, SclerodermaView all (22 more) |
|
292
|
|
|
Solute carrier family 7 member 8 |
LAT2, LPI-PC1 |
|
|
293
|
|
|
Solute carrier family 35 member A3 |
AMRS |
Arthrogryposis multiplex congenita, Arthrogryposis, mental retardation, and seizures, Autism spectrum disorder-epilepsy-arthrogryposis syndrome, Autism, Central nervous system neoplasms, Developmental delay, Glioma, Mental retardation, Microcephaly, Scoliosis |
|
294
|
|
|
Splicing factor 3b subunit 1 |
Hsh155, MDS, PRP10, PRPF10, SAP155, SF3b155 |
Adenocarcinoma, Agranulocytosis, Anemia, Anemia with ringed sideroblasts, Mammary neoplasms, Cataract, Choroidal melanoma, Congenital cataract, Congestive heart failure, Dysplastic granulopoesis, Hypochromic anemia, Inferior lens subluxation, Inflammatory abnormality of the eye, Iris melanoma, Lymphocytic leukemia, Leukemia, Liver carcinoma, Ciliary body melanoma, Malignant mesothelioma, Malignant neoplasm, Melanoma, Myelodysplasia, Myelodysplastic syndrome, Neutropenia, Ocular hypertension, Pancytopenia, Prostatic neoplasms, Prostate cancer, Renal carcinoma, Retinal detachment, Schizophrenia, Thrombocytosis, Bladder carcinoma, Uveal melanomaView all (19 more) |
|
295
|
|
|
SEC11 homolog A, signal peptidase complex subunit |
1810012E07Rik, SEC11L1, SPC18, SPCS4A, sid2895 |
|
|
296
|
|
|
SUZ12 polycomb repressive complex 2 subunit |
CHET9, IMMAS, JJAZ1 |
Adenoma, Congenital clubfoot, Congenital hypoplasia of penis, Cryptorchidism, Developmental delay, Endometrial neoplasms, Endometrial carcinoma, Endometrial stromal sarcoma, Giant cell glioblastoma, Glioblastoma, Glioma, Macrocephaly, Macrotia, Malignant neoplasm, Melanocytic nevus, Melanoma, Mental retardation, Micrognathism, Nerve sheath tumors, Neurilemmoma, Neurofibroma, Peripheral nerve sheath neoplasm, Papillary adenoma, Perineurioma, Schwannomatosis, Scoliosis, Syndactyly of fingers, Talipes transversoplanus, Urogenital abnormalities, Weaver syndromeView all (15 more) |
|
297
|
|
|
Scaffold protein involved in DNA repair |
KIAA0146, ODG9 |
46, xx gonadal dysgenesis, 46,xx gonadal dysgenesis, Arachnodactyly, Dwarfism, Gonadal dysgenesis, Microcephaly, Osteopenia, Osteoporosis of vertebrae, Physiologic amenorrhea, Premature menopause, Pulmonary fibrosis, Secondary physiologic amenorrhea, Streak ovary |
|
298
|
|
|
Solute carrier family 39 member 14 |
HCIN, HMNDYT2, LZT-Hs4, NET34, ZIP14, cig19 |
Cerebellar atrophy, Cerebral atrophy, Developmental delay, Developmental regression, Dyskinetic syndrome, Dystonia-parkinsonism-hypermanganesemia syndrome, Facial paralysis, Hearing loss, Hypermanganesemia with dystonia, Mental retardation, Optic atrophy, Parkinson disease, Scoliosis |
|
299
|
|
|
Solute carrier family 16 member 8 |
MCT3, REMP |
|
|
300
|
|
|
Seizure related 6 homolog like |
SEZ6L1 |
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