|
151
|
|
|
Mitochondrial transcription termination factor 4 |
MTERFD2 |
|
|
152
|
|
|
Methyltransferase 6, tRNA N3-cytidine |
hMETTL6 |
|
|
153
|
|
|
Mitogen-activated protein kinase kinase kinase 8 |
AURA2, COT, EST, ESTF, MEKK8, TPL2, Tpl-2, c-COT |
|
|
154
|
|
|
Mucin like 3 |
C6orf37, DPCR1, PBLT |
Attention deficit hyperactivity disorder, Bipolar disorder, Coronary heart disease, Development disorder, Diabetes mellitus, Diffuse panbronchiolitis, Lung adenocarcinoma, Lung cancer, Lupus erythematosus, Membranous glomerulonephritis, Mental depression, Myasthenia gravis, Rheumatoid arthritis, Schizophrenia, Vitiligo |
|
155
|
|
|
M-phase specific PLK1 interacting protein |
ABHS, C7orf11, ORF20, TTD4 |
Amish brittle hair brain syndrome, Anemia, Astigmatism, Breast cancer, Bronchospasm, Carcinoma, Cardiomyopathy, Cerebral cortical atrophy, Clastothrix, Congenital epicanthus, Congenital exfoliative erythroderma, Congenital exomphalos, Craniosynostosis, Cryptorchidism, Dental enamel hypoplasia, Developmental delay, Dysarthria, Ectropion, Eczema, Esotropia, Gonadal dysgenesis, Hypoplasia of mandible relative to maxilla, Ichthyosis, Impaired social reciprocity, Keratoconjunctivitis sicca, Macrotia, Age-related macular degeneration, Mental retardation, Microcephaly, Microcornea, Microphthalmos, Myopia, Nervous system diseases, Neutropenia, Nystagmus, Osteopenia, Osteosclerosis, Paraplegia, Partial agenesis of corpus callosum, Periventricular leukomalacia, Seizure, Sensorineural hearing loss, Trichorrhexis nodosa syndrome, Trichothiodystrophy, Ventricular septal defectView all (30 more) |
|
156
|
|
|
MAGE family member C3 |
CT7.2, HCA2, MAGE-C3, MAGEC4 |
|
|
157
|
|
|
Myosin IIIB |
- |
|
|
158
|
|
|
Mono-ADP ribosylhydrolase 2 |
C20orf133, C2orf133 |
|
|
159
|
|
|
MIB E3 ubiquitin protein ligase 2 |
ZZANK1, ZZZ5 |
|
|
160
|
|
|
MAGUK p55 scaffold protein 7 |
- |
|
