Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "M"
811 to 820 of 898 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

811
MYCL proto-oncogene, bHLH transcription factor
L-Myc, LMYC, MYCL1, bHLHe38
Medulloblastoma, Metabolic syndrome, Prostatic neoplasm, Small cell lung carcinoma, Diabetes mellitus, type 2

812
MYCN proto-oncogene, bHLH transcription factor
FGLDS1, MODED, MPAPA, MYCNsORF, MYCNsPEP, N-myc, NMYC, ODED, bHLHe37
Adenoid cystic carcinoma, Basal cell carcinoma, Desbuquois syndrome, Double outlet right ventricle, Feingold syndrome, Gallbladder agenesis, Hyperplasia, Medulloblastoma, Necrosis, Neuroblastoma, Ventricular septal defect, Wilms tumor

813
MYC target 1
MTLC
Uterine fibroid

814
MYD88 innate immune signal transduction adaptor
IMD68, MYD88D, WM1
Cholelithiasis, Depression, Eosinophilia, Hypertension, Immunodeficiency, Lymphoma, Diffuse large b-cell lymphoma, Waldenstrom macroglobulinemia

815
Myeloid derived growth factor
C19orf10, EUROIMAGE1875335, IL25, IL27, IL27w, R33729_1, SF20
Alzheimer disease

816
Myeloma overexpressed
OCIM
Androgenetic alopecia, Aortic stenosis, Aortic valve disease, Atrial fibrillation, Brain aneurysm, Breast cancer, Cancer, Cardiovascular disease, Cataract, Clear cell renal cell carcinoma, Colorectal cancer, Estrogen-receptor negative breast cancer, Hearing loss, Kidney cancer, Lung cancer
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817
Myogenic factor 5
EORVA, bHLHc2
Scoliosis

818
Myogenic factor 6
CNM3, MRF4, bHLHc4, myf-6
Centronuclear myopathy, Congenital structural myopathy

819
Myosin heavy chain 10
NMMHC-IIB, NMMHCB
Autism, Coloboma, Neurodevelopmental disorder, Congenital fibrosis of extraocular muscles, Congenital ocular coloboma, Congenital ptosis, Focal glomerulosclerosis, Major depressive disorder, Diabetes mellitus, type 2, Visual disorder

820
Myosin heavy chain 11
AAT4, FAA4, SMHC, SMMHC, SMMS-1, VSCM2
Aortic aneurysm, Atrial fibrillation, Bicuspid aortic valve, Intestinal pseudo-obstruction, Congenital aneurysm of ascending aorta, Congenital heart disease, Connective tissue disease, Coronary artery disease, Ehlers-danlos syndrome, Thoracic aortic aneurysm and aortic dissection, Heart failure, Hemorrhoid, Left ventricular disease, Myeloid leukemia, Lissencephaly
View all (12 more)