1201
|
|
|
Solute carrier family 25 member 1 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
1202
|
|
|
Solute carrier family 25 member 1 pseudogene 3 |
- |
Curated: N/A
Unreviewed: N/A
|
1203
|
|
|
Solute carrier family 25 member 1 pseudogene 4 |
- |
Curated: N/A
Unreviewed: N/A
|
1204
|
|
|
Solute carrier family 25 member 1 pseudogene 5 |
- |
Curated: N/A
Unreviewed: N/A
|
1205
|
|
|
Solute carrier family 25 member 2 |
ORC2, ORNT2 |
Curated: Obesity
Unreviewed: Carcinogenesis, Hyperammonemia, Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome, Liver failure, Osteosarcoma, Renal Carcinoma
|
1206
|
|
|
Solute carrier family 25 member 20 |
CAC, CACT |
Curated: Autism, Carnitine acetyltransferase deficiency, Insomnia
Unreviewed: Acyl CoA Dehydrogenase Deficiency, Adrenal Gland Pheochromocytoma, Arteriosclerosis, Asthma, Atherosclerosis, Atrial Fibrillation, Atrioventricular block, Behavioral Variant Of Frontotemporal Dementia, beta Thalassemia, Brain disease, Breast Cancer, Breast Carcinoma, Burkitt`s Lymphoma, Carcinogenesis, Cardiomyopathy, Cardiovascular Diseases, Carnitine palmitoyl transferase deficiency, Carnitine palmitoyltransferase deficiency, Carnitine-Acylcarnitine Translocase Deficiency, Cervical Intraepithelial Neoplasia, Cervix carcinoma, Chronic Obstructive Pulmonary Disease, Cognitive disorder, Colitis, Colonic Neoplasms, Colorectal Cancer, Colorectal neoplasm, Coronary Arteriosclerosis, Coronary artery disease, Coronary Heart Disease, Crohn Disease, Cytochrome-C Oxidase Deficiency, Developmental Delay, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 2, Epileptic encephalopathy, Esophagus Neoplasm, Frontotemporal dementia, Gestational diabetes, Glycogen Storage Disease, Hepatocellular carcinoma, Hermansky-Pudlak Syndrome, Hyperparathyroidism, Hypertension, Hypoglycemia, Inborn Errors Of Metabolism, Inflammatory Bowel Disease, Leukemia, Liver carcinoma, Liver failure, Liver neoplasm, Malignant Neoplasm, Mental Depression, Microcephaly, Mitochondrial Diseases, Mitochondrial trifunctional protein deficiency, Multiple Acyl-CoA Dehydrogenase Deficiency, Multiple Sclerosis, Myelofibrosis, Myocardial Infarction, Neoplasms, Nystagmus, Osteoporosis, Parkinson disease, Phobic Anxiety Disorder, Prostate cancer, Psoriasis, Rheumatic Heart Disease, Schizophrenia, Sleep Apnea, ST Segment Elevation Myocardial Infarction, Sudden episodic apnea, Tarsal-Carpal Coalition Syndrome, Ulcerative colitis, Urinary bladder neoplasms, Ventricular hypertrophy, Ventricular tachycardia, Wiskott-Aldrich Syndrome, Zellweger Syndrome
|
1207
|
|
|
Solute carrier family 25 member 20 pseudogene 1 |
CACTP, SLC25A20P |
Curated: N/A
Unreviewed: N/A
|
1208
|
|
|
Solute carrier family 25 member 21 |
MTDPS18, ODC, ODC1 |
Curated: Barrett esophagus, Breast cancer, Colorectal cancer, Coronary artery disease, Esophageal adenocarcinoma, Estrogen-receptor negative breast cancer, Migraine, Mitochondrial dna depletion syndrome, Ovarian cancer, Prostate cancer
Unreviewed: Adenocarcinoma, Adenoma, Alopecia, Alzheimer disease, Angiolymphoid Hyperplasia, Anxiety disorder, Arthritis, Asthma, Atrial fibrillation, Benign Prostatic Hyperplasia, Bicuspid aortic valve, Bipolar disorder, Brain disease, Breast Cancer, Breast Carcinoma, Breast neoplasm, Brooke-Spiegler Syndrome, Cap myopathy, Carcinogenesis, Carcinoma, Carcinoma Of The Head And Neck, Cardiovascular disease, Cerebral Infarction, Colitis, Coloboma of optic disc, Colon Carcinoma, Colonic disease, Colonic neoplasm, Colonic Neoplasms, Colorectal adenoma, Colorectal Cancer, Colorectal neoplasm, Colorectal Neoplasms, Crohn Disease, Developmental Delay, Developmental disability, Diabetes Mellitus, Dwarfism, Ectodermal Dysplasia, Endocarditis, Endometrial Cancer, Endometrial carcinoma, Epilepsy, Epithelioma, Esophageal Cancer, Esophageal Carcinoma, Esophageal squamous cell carcinoma, Esophagus Neoplasm, Fibrosarcoma, Gastritis, Gastrointestinal disease, Glioblastoma, Glioma, Global Developmental Delay-Alopecia-Macrocephaly-Facial Dysmorphism-Structural Brain Anomalies Syndrome, Headache, Hepatocellular carcinoma, Hyperammonemia, Hypersensitivity, Hypertension, Inclusion body myopathy, Inflammatory Bowel Disease, Intellectual developmental disorder, Kidney Cancer, Kidney Failure, Leukemia, Lichen amyloidosis, Liver Cancer, Liver carcinoma, Liver neoplasms, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Lung disease, Lung Neoplasms, Lymphocytic Leukemia, Lymphoid leukemia, Lymphoma, Macrocephaly, Malignant gastrointestinal tract tumors, Malignant Neoplasm, Mammary Neoplasms, Megalencephalic Leukoencephalopathy With Subcortical Cysts, Memory disorders, Meningioma, Mental retardation, Miscarriage, Mitochondrial disease, Mitochondrial myopathy, Mood disorder, Multiple myeloma, Multiple polyposis syndrome, Myeloid Leukemia, Myeloproliferative disorder, Myotonic dystrophy, Nasopharyngeal Carcinoma, Neoplasms, Neuroblastoma, Neurodevelopmental Disorders, Neuroendocrine Tumors, Osteosarcoma, Otitis media, Ovarian neoplasm, Overactive bladder, Pancreatic adenocarcinoma, Pancreatic cancer, Pancreatic carcinoma, Pancreatic Neoplasm, Papilloma, Papillomatosis, Peutz-Jeghers Syndrome, Polyp, Promyelocytic Leukemia, Prostatic neoplasm, Prostatic Neoplasms, Renal Carcinoma, Renal cell carcinoma, Retinoblastoma, Rhabdomyosarcoma, Rheumatoid arthritis, Schizophrenia, SEBASTIAN SYNDROME, Seizures, Skin cancer, Skin carcinoma, Skin Neoplasms, Small cell lung carcinoma, Spinal Muscular Atrophy, Squamous cell carcinoma, Stomach Carcinoma, Stomach disease, Stomach Diseases, Stomach Neoplasms, Stroke, Sveinsson Chorioretinal Atrophy, Triple negative breast cancer, Ulcerative colitis, Urinary bladder neoplasms, Xeroderma Pigmentosum
|
1209
|
|
|
SLC25A21 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
1210
|
|
|
SLC25A21 antisense RNA 2 |
- |
Curated: N/A
Unreviewed: N/A
|