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"
881 to 890 of 898 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

881
Myomesin 2
TTNAP
Ankylosing spondylitis, Bipolar disorder, Cervical cancer, Major depressive disorder, Pelvic organ prolapse, Schizophrenia, Amyotrophic lateral sclerosis, Diabetes mellitus type 2

882
Myomesin 3
-
Bipolar disorder, Diabetes mellitus type 2

883
Myogenesis regulating glycosidase
IBGC7, KIAA1161, NET37
Idiopathic basal ganglia calcification, Primary familial brain calcification, Diabetic retinopathy, Dysarthria, Fahr's disease, Gout

884
Myotilin
LGMD1, LGMD1A, MFM3, TTID, TTOD
Atrial fibrillation, Cardiomyopathy, Distal amyotrophy, Distal myotilinopathy, Muscular dystrophy, Myofibrillar myopathy, Non-neoplastic peripheral nervous system disease, Peripheral nervous system disease, Peripheral neuropathy

885
Myozenin 1
CS-2, FATZ, MYOZ
Atrial fibrillation

886
Myozenin 2
C4orf5, CMH16, CS-1, FATZ-2
Alzheimer disease, Attention deficit hyperactivity disorder, Cardiomyopathy, Hypertrophic cardiomyopathy, Diabetes mellitus type 2

887
Myopalladin
CMD1DD, CMH22, CMYO24, CMYP24, MYOP, NEM11, RCM4
Alzheimer disease, Atrial fibrillation, Cap myopathy, Cardiomyopathy, Dilated cardiomyopathy, Nemaline myopathy, Kidney disease, Obstructive pulmonary disease, Congenital myopathy, Restrictive cardiomyopathy, Gastroesophageal reflux disease, Hypertrophic cardiomyopathy, Inflammatory bowel disease, Left ventricular disease, Left ventricular noncompaction cardiomyopathy
View all (1 more)

888
Myb related transcription factor, partner of profilin
P42pop
Neurotic disorder, Osteoarthritis, Diabetes mellitus type 2

889
Myelin regulatory factor
11orf9, C11orf9, CUGS, MMERV, MRF, NNO1, Ndt80, pqn-47
Ankylosing spondylitis, Aortic stenosis, Asthma, Eczema, Neoplasms, Bipolar disorder, Cardiac-urogenital syndrome, Ischemic stroke, Colorectal adenoma, Colorectal cancer, Congenital diaphragmatic hernia, Congenital heart defects, Coronary artery disease, Crohn disease, Developmental disability
View all (20 more)

890
Myelin regulatory factor like
C12orf15, C12orf28, bcm1377
Attention deficit hyperactivity disorder, Conduct disorder, Osteoarthritis