241
|
|
|
Minichromosome maintenance complex binding protein |
C10orf119, MCM-BP |
|
242
|
|
|
Minichromosome maintenance domain containing 2 |
C8orf45 |
|
243
|
|
|
Mucolipin TRP cation channel 1 |
LECD, MG-2, ML1, ML4, MLIV, MST080, MSTP080, TRP-ML1, TRPM-L1, TRPML1 |
|
244
|
|
|
Microcephalin 1 |
BRIT1, MCT |
Atherosclerosis, Primary microcephaly, Color vision deficiency, Congenital microcephaly, Congenital neurologic anomalies, Dental caries, Global developmental delay, Hereditary breast cancer, Intellectual developmental disorder, Kidney cancer, Lymphatic malformation, Microcephaly, Open angle glaucoma |
245
|
|
|
MAPK regulated corepressor interacting protein 1 |
FAM195B, GRAN2, MCRIP |
|
246
|
|
|
MAPK regulated corepressor interacting protein 2 |
C16orf14, FAM195A, c349E10.1 |
|
247
|
|
|
Microspherule protein 1 |
ICP22BP, INO80Q, MCRS2, MSP58, P78 |
|
248
|
|
|
Multiple C2 and transmembrane domain containing 1 |
- |
Anorexia nervosa, Attention deficit hyperactivity disorder, Bipolar disorder, Breast cancer, Eating disorder, Head and neck neoplasm, Hypertrophic cardiomyopathy, Keratoconus, Metabolic syndrome, Multiple sclerosis, Enterocolitis, Neuromuscular disease, Peripheral arterial disease, Substance abuse, Diabetes mellitus type 2 |
249
|
|
|
Multiple C2 and transmembrane domain containing 2 |
- |
Alzheimer disease, Attention deficit hyperactivity disorder, Congenital heart disease, Coronary artery disease, Dementia, Chromosome 15q deletion syndrome, Major depressive disorder, Nephrolithiasis, Parkinson disease, Schizophrenia, Tetralogy of fallot, Depression |
250
|
|
|
MCTS1 re-initiation and release factor |
IMD118, MCT-1, MCT1 |
|
