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"
871 to 880 of 893 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

871
Myocilin opposite strand
-
Alzheimer disease, Atrial fibrillation, Glaucoma, Open angle glaucoma

872
Myogenic differentiation 1
CMYO17, CMYP17, MYF3, MYOD, MYODRIF, PUM, bHLHc1
Arthrogryposis multiplex congenita, Congenital myopathy, Fetal akinesia deformation sequence, Hodgkin lymphoma, Pena-shokeir syndrome , Rhabdomyosarcoma

873
Myoferlin
FER1L3, HAE7
Angioedema, Hereditary angioedema

874
Myogenin
MYF4, bHLHc3, myf-4
Asthma

875
Myomesin 1
SKELEMIN
Arrhythmogenic right ventricular cardiomyopathy, Cardiac arrest, Cardiomyopathy, Dilated cardiomyopathy, Non-immune hydrops fetalis, Hypertrophic cardiomyopathy, Hypoglycemia, Scoliosis

876
Myomesin 2
TTNAP
Ankylosing spondylitis, Bipolar disorder, Cervical cancer, Major depressive disorder, Pelvic organ prolapse, Schizophrenia, Amyotrophic lateral sclerosis, Diabetes mellitus type 2

877
Myomesin 3
-
Bipolar disorder, Diabetes mellitus type 2

878
Myogenesis regulating glycosidase
IBGC7, KIAA1161, NET37
Idiopathic basal ganglia calcification, Primary familial brain calcification, Diabetic retinopathy, Dysarthria, Fahr's disease, Gout

879
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

880
Myozenin 1
CS-2, FATZ, MYOZ
Atrial fibrillation