Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "M"
811 to 820 of 893 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

811
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
View all (5 more)

812
Myogenic factor 5
EORVA, bHLHc2
Scoliosis

813
Myogenic factor 6
CNM3, MRF4, bHLHc4, myf-6
Centronuclear myopathy, Congenital structural myopathy

814
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

815
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)

816
Myosin heavy chain 13
MyHC-IIL, MyHC-eo
Coronary artery disease, Major depressive disorder, Neuroblastoma, Open angle glaucoma, Osteoarthritis, Periodontitis

817
Myosin heavy chain 14
DFNA4, DFNA4A, FP17425, MHC16, MYH17, NMHC II-C, NMHC-II-C, PNMHH, myosin
Isolated sensorineural deafness, Nonsyndromic hearing loss, Dilated cardiomyopathy, Charcot-marie-tooth disease, Deafness, Dental enamel hypoplasia, Hearing impairment, Hereditary hearing loss, Meniere disease, Peripheral neuropathy myopathy hoarseness hearing loss syndrome, Peripheral neuropathy, Peripheral neuropathy, myopathy, hoarseness, and hearing, Prostatic neoplasms, Hearing loss

818
Myosin heavy chain 15
-
Anxiety disorder, Bipolar disorder, Hypothyroidism, Insomnia, Major depressive disorder, Metabolic syndrome, Microcephaly, Diabetes mellitus type 2

819
Myosin heavy chain 16
MHC20, MYH16P, MYH5
Leukemia

820
Myosin heavy chain 2
CMYO6, CMYP6, IBM3, MYH2A, MYHSA2, MYHas8, MYPOP, MyHC-2A, MyHC-IIa
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia, Congenital myopathy, Muscular dystrophy, Myopathy, Myositis