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"
841 to 850 of 893 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

841
Myomaker, myoblast fusion factor
MYOMAKER, TMEM226, TMEM8C
Alzheimer disease, Aortic stenosis, Aortic valve disease, Carey-fineman-ziter syndrome, Major salivary gland carcinoma

842
Myomixer, myoblast fusion factor
CFZS2, MINION, hMINION
Carey-fineman-ziter syndrome

843
Myoneurin
OSZF, SBBIZ1, ZBTB31, ZNF902
Celiac disease, Central nervous system cancer, Lymphocytic leukemia, Osteomyelitis, Clear cell renal cell carcinoma, Colorectal cancer, Melanoma, Glioma, Kidney cancer, Leukemia, Lung cancer, Lymphoid leukemia, Multiple myeloma, Multiple sclerosis, Myeloproliferative disorder
View all (5 more)

844
Myosin X
MyoX
Major depressive disorder, Obesity, Polycystic ovary syndrome

845
Myosin XVA
DFNB3, MYO15
Alzheimer disease, Isolated sensorineural deafness, Nonsyndromic hearing loss, Basal cell carcinoma, Congenital ear anomaly, Congenital sensorineural hearing loss, Deafness, Hearing impairment, Hearing loss, Hemorrhoid, Hereditary hearing loss, Non-melanoma skin carcinoma, Obesity

846
Myosin XVB
MYO15BP
Color vision deficiency, Congenital myopathy

847
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
View all (2 more)

848
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

849
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

850
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