Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
8261 to 8270 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

8261
Myeloid derived growth factor
C19orf10, EUROIMAGE1875335, IL25, IL27, IL27w, R33729_1, SF20
Alzheimer disease

8262
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)

8263
Myogenic factor 5
EORVA, bHLHc2
Scoliosis

8264
Myogenic factor 6
CNM3, MRF4, bHLHc4, myf-6
Centronuclear myopathy, Congenital structural myopathy

8265
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

8266
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)

8267
Myosin heavy chain 13
MyHC-IIL, MyHC-eo
Coronary artery disease, Major depressive disorder, Neuroblastoma, Open angle glaucoma, Osteoarthritis, Periodontitis

8268
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

8269
Myosin heavy chain 15
-
Anxiety disorder, Bipolar disorder, Hypothyroidism, Insomnia, Major depressive disorder, Metabolic syndrome, Microcephaly, Diabetes mellitus type 2

8270
Myosin heavy chain 16
MHC20, MYH16P, MYH5
Leukemia