791
|
|
|
MAX interactor 1, dimerization protein |
MAD2, MXD2, MXI, bHLHc11 |
|
792
|
|
|
Matrix remodeling associated 5 |
- |
|
793
|
|
|
Matrix remodeling associated 8 |
ASP3 |
|
794
|
|
|
Myeloid associated differentiation marker |
SB135 |
|
795
|
|
|
MYB proto-oncogene, transcription factor |
Cmyb, c-myb, c-myb_CDS, efg |
Androgenetic alopecia, Angiocentric glioma, Asthma, B-cell acute lymphoblastic leukemia, Adenoid cystic carcinoma, Cardiovascular disease, Deficiency anemia, Glioma, Hemoglobin e disease, Hyperlipidemia, Hypothyroidism, Metabolic syndrome, Multiple sclerosis, Myeloproliferative disorder, Neuroblastoma, ObesityView all (1 more) |
796
|
|
|
MYB binding protein 1a |
P160, PAP2, Pol5 |
|
797
|
|
|
MYB proto-oncogene like 1 |
A-MYB, AMYB |
|
798
|
|
|
MYB proto-oncogene like 2 |
B-MYB, BMYB |
|
799
|
|
|
Myosin binding protein C1 |
CMYO16, CMYP16, LCCS4, MYBPCC, MYBPCS, MYOTREM, ssMyBP-C |
|
800
|
|
|
Myosin binding protein C3 |
CMD1MM, CMH4, FHC, LVNC10, MYBP-C, cMyBP-C |
Arrhythmogenic right ventricular cardiomyopathy, Asymmetric septal hypertrophy, Atrial fibrillation, Brugada syndrome, Cardiomegaly, Cardiomyopathy, Dilated cardiomyopathy, Cardiovascular abnormalities, Cardiovascular disease, Concentric hypertrophic cardiomyopathy, Congenital heart disease, Hypertrophic cardiomyopathy, Hirschsprung disease, Hypertension, Intellectual developmental disorder, Left ventricular disease, Left ventricular noncompaction cardiomyopathy, Long qt syndrome, Multiple sclerosis, Paroxysmal atrial fibrillation, Peripheral neuropathy, Polymorphic catecholaminergic ventricular tachycardia, Schizophrenia, Catecholaminergic polymorphic ventricular tachycardia, Wolff-parkinson-white syndromeView all (10 more) |