3381
|
|
|
Mitochondrial ribosomal protein S7 |
COXPD34, MRP-S, MRP-S7, RP-S7, RPMS7, S7mt, bMRP27a, uS7m |
Curated: Breast neoplasms, Combined oxidative phosphorylation deficiency, Nonalcoholic fatty liver disease, Hearing loss, mitochondrial disease
Unreviewed: Addison`s Disease, Breast Cancer, Breast Carcinoma, Breast neoplasm, Combined Oxidative Phosphorylation Deficiency, Congenital Sensorineural Hearing Loss, Fatty Liver, Hepatocellular carcinoma, Hypoglycemia, Hypogonadism, Ischemic stroke, Kidney Failure, Liver failure, Mammary Neoplasms, Marfan Syndrome, Melas syndrome, Osteosarcoma, Pancytopenia, Syndromic Sensorineural Deafness
|
3382
|
|
|
Mitochondrial ribosomal protein S7 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
3383
|
|
|
Mitochondrial ribosomal protein S7 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
3384
|
|
|
Mitochondrial ribosomal protein S9 |
MRP-S9, RPMS9, S9mt, uS9m |
Curated: N/A
Unreviewed: Colorectal neoplasm, Ischemic stroke, Renal cell carcinoma
|
3385
|
|
|
MRPS9 antisense RNA 1 |
UTAT33 |
Curated: N/A
Unreviewed: N/A
|
3386
|
|
|
MRPS9 antisense RNA 2 |
- |
Curated: N/A
Unreviewed: N/A
|
3387
|
|
|
Mitochondrial ribosome recycling factor |
MRFF, MTRRF, RRF |
Curated: N/A
Unreviewed: Cytochrome-C Oxidase Deficiency, Mitochondrial disease, Mitochondrial trifunctional protein deficiency, Myopathy
|
3388
|
|
|
Mitochondrial ribosome recycling factor pseudogene 1 |
MRRFP |
Curated: N/A
Unreviewed: N/A
|
3389
|
|
|
Magnesium transporter MRS2 |
HPT, MRS2L |
Curated: N/A
Unreviewed: Adenoma, Atherosclerosis, Benign Neoplasm, beta Thalassemia, Bipolar Disorder, Bone Disease, Breast neoplasm, CADASIL Syndrome, Carcinogenesis, Cerebral Infarction, Charcot-Marie-Tooth Disease, Corticobasal degeneration, Dental Enamel Hypoplasia, Deuteranomaly, Diabetes Mellitus, Diabetes mellitus, type 2, Diabetic Nephropathy, Dysphagia, Facial dysmorphism, Glomerulonephritis, Hearing Loss, Hereditary cancer, Humoral Hypercalcemia Of Malignancy, Hypercalcemia, Hyperparathyroidism, Hyperparathyroidism-Jaw Tumor Syndrome, Hyperphosphatemia, Hypertension, Hypocalciuric Hypercalcemia, Hypoparathyroidism, Hypoparathyroidism-deafness-renal disease syndrome, Hypothyroidism, Idiopathic pulmonary fibrosis, Ischemic Stroke, Isolated Somatotropin Deficiency, Kenny-Caffey Syndrome, Kidney Disease, Mental Depression, Multiple Endocrine Neoplasia, Multiple Sclerosis, Neoplasms, Pancreatitis, Paraganglioma, Parathyroid Gland Adenocarcinoma, Parathyroid Neoplasms, Polyglandular autoimmune syndrome, Polyposis Syndrome, Pseudohypoparathyroidism, Renal dysplasia, Sarcopenia, Skin Erosion, Somatotropin Deficiency, Stroke, Subarachnoid hemorrhage, Thyroid cancer, Thyroid Carcinoma, Thyroid Neoplasm, Uremia, Von Hippel-Lindau Syndrome
|
3390
|
|
|
MRS2 pseudogene 1 |
MRS2LP1 |
Curated: N/A
Unreviewed: N/A
|