651
|
|
|
MicroRNA 425 |
MIRN425, hsa-mir-425, mir-425 |
|
652
|
|
|
Misshapen like kinase 1 |
B55, MAP4K6, MEKKK 6, MINK, YSK2, ZC3 |
|
653
|
|
|
Myelin expression factor 2 |
HsT18564, MEF-2, MST156, MSTP156, myEF-2 |
|
654
|
|
|
- |
MYMY |
|
655
|
|
|
Mitochondrial ribosomal protein S16 |
CGI-132, COXPD2, MRP-S16, RPMS16, S16mt, bS16m |
|
656
|
|
|
Mitochondrial ribosomal protein S18C |
CGI-134, MRP-S18-1, MRP-S18-c, MRPS18-1, S18mt-c, bS18m, mrps18-c |
|
657
|
|
|
Mediator of cell motility 1 |
C2orf4, CGI-27, MEMO, NS5ATP7 |
|
658
|
|
|
Mitochondrial ribosomal protein S7 |
COXPD34, MRP-S, MRP-S7, RP-S7, RPMS7, S7mt, bMRP27a, uS7m |
Addison`s disease, Breast cancer, Mammary neoplasms, Breast carcinoma, Combined oxidative phosphorylation deficiency, Fatty liver, Hypoglycemia, Hypogonadism, Liver failure, Marfan syndrome, Pancytopenia, Syndromic sensorineural deafness |
659
|
|
|
MLX interacting protein like |
CHREBP, MIO, MLX, MONDOB, WBSCR14, WS-bHLH, bHLHd14 |
Acquired kyphoscoliosis, Anxiety disorder, Attention deficit hyperactivity disorder, Bicuspid aortic valve, Bladder diverticulum, Blepharophimosis, Congenital epicanthus, Congenital kyphoscoliosis, Coronary stenosis, Cutis laxa, Diabetes mellitus, Dwarfism, Food intolerance, Gastroesophageal reflux disease, Gout, Gouty arthritis, Hearing loss, Hypertension, Hypodontia, Kidney failure, Liver carcinoma, Mental retardation, Metabolic syndrome, Microdontia, Obesity, Osteopenia, Osteoporosis, Otitis media, Pelvic kidney, Peripheral pulmonary artery stenosis, Pulmonary stenosis, Rectal prolapse, Renal hypoplasia, Renal insufficiency, Strabismus, Supravalvar aortic stenosis, Vesicoureteral reflux, Williams syndromeView all (23 more) |
660
|
|
|
Mitochondrial trans-2-enoyl-CoA reductase |
CGI-63, DYTOABG, ETR1, FASN2B, NRBF1, OPA16 |
Cerebral palsy, Craniofacial dystonia, Developmental delay, Dysarthria, Dyskinetic syndrome, Dysphagia, Dystonia, Dystonia with optic atrophy and basal ganglia abnormalities, Mepan syndrome, Nystagmus, Optic atrophy |