Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "M"
851 to 860 of 898 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

851
Myosin XVB
MYO15BP
Color vision deficiency, Congenital myopathy

852
Myosin XVI
MYAP3, MYR8, Myo16b, NYAP3, PPP1R107
Alzheimer disease, Bipolar disorder, Colorectal cancer, Dementia, Dental caries, Glaucoma, Osteonecrosis of the femoral head, Insomnia, Metabolic syndrome, Obesity, Open angle glaucoma, Oropharyngeal cancer, Prostate cancer, Schizophrenia, Scoliosis
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853
Myosin XVIIIA
MAJN, MYSPDZ, SP-R210, SPR210, TIAF1
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Colorectal cancer, Contracture of multiple joints, Hydrops fetalis, Major depressive disorder, Obsessive-compulsive disorder, Schizophrenia, Tourette syndrome

854
Myosin XVIIIB
KFS4
Atrial fibrillation, Bipolar disorder, Brugada syndrome, Desbuquois syndrome, Fraser syndrome, Genetic predisposition to disease, Klippel-feil syndrome, Lung neoplasms, Major depressive disorder, Mesothelioma, Nemaline myopathy, Ovarian cancer, Ovarian serous carcinoma, Scoliosis, Uterine fibroid

855
Myosin XIX
MYOHD1
Anorexia nervosa, Attention deficit hyperactivity disorder, Bipolar disorder, Kidney disease, Global developmental delay, Glycosylphosphatidylinositol biosynthesis defect, Obesity, Schizophrenia, Tourette syndrome, Diabetes mellitus, type 2, Uranostaphyloschisis

856
Myosin IA
BBMI, DFNA48, DIAR15, MIHC, MYHL
Asthma, Nonsyndromic hearing loss, Congenital chloride diarrhea, Deafness, Hereditary hearing loss, Insomnia, Migraine, Hearing loss

857
Myosin IB
MMI-alpha, MMIa, MYH-1c, myr1
Esophageal squamous cell carcinoma, Hepatomegaly, Obesity, Oligodendroglioma, Open angle glaucoma, Pancreatic cancer, Scoliosis, Hypertension

858
Myosin IC
MMI-beta, MMIb, MyoIC, NMI, myr2
Alzheimer disease, Atrial fibrillation, Isolated sensorineural deafness, Nonsyndromic hearing loss, Heart failure, Liver cirrhosis, Meniere disease, Miller-dieker syndrome

859
Myosin ID
PPP1R108, myr4
Anorexia nervosa, Autism, Dupuytren contracture, Eating disorder, Hypertension, Metabolic syndrome, Pancreatic cancer

860
Myosin IE
FSGS6, HuncM-IC, MYO1C
Alzheimer disease, Anorexia nervosa, Attention deficit hyperactivity disorder, Dementia, Dupuytren contracture, Idiopathic steroid-resistant nephrotic syndrome, Focal glomerulosclerosis, Focal segmental glomerulosclerosis, Genetic steroid-resistant nephrotic syndrome, Hereditary steroid-resistant nephrotic syndrome, Major depressive disorder, Metabolic syndrome, Nephrotic syndrome, Nephrotic syndrome, focal segmental type, Schizophrenia
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