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"
511 to 520 of 893 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

511
Motor neuron and pancreas homeobox 1
HB9, HLXB9, HOXHB9, SCRA1
Currarino syndrome, Desbuquois syndrome, Permanent neonatal diabetes mellitus, Gastroparesis, Neonatal diabetes mellitus, Scoliosis, Diabetes mellitus type 2

512
Modulator of apoptosis 1
MAP-1, PNMA4
Endometriosis, Gout

513
MOB kinase activator 1A
C2orf6, MABKL1B, MATS1, MOB1, MOBK1B, MOBKL1B, Mob4B
Alzheimer disease

514
MOB kinase activator 1B
MATS2, MOB4A, MOBKL1A
Alzheimer disease, Atrial fibrillation, Kidney disease, Diabetes mellitus, Kidney failure, Diabetes mellitus type 2

515
MOB kinase activator 2
HCCA2
Diverticular disease, Prostate cancer

516
MOB kinase activator 3B
C9orf35, MOB1D, MOBKL2B
Alzheimer disease, Amyotrophic lateral sclerosis, Asthma, Eye neoplasms, Dementia, Diverticular disease, Frontotemporal dementia, Hemolytic anemia, Major depressive disorder, Obesity, Osteoarthritis, Diabetes mellitus type 2

517
MOB kinase activator 3C
MOB1E, MOBKL2C
Kidney disease, Hypertension, Sinusitis

518
MOB family member 4, phocein
2C4D, CGI-95, MOB1, MOB3, MOBKL3, PHOCN, PREI3
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Insomnia, Major depressive disorder, Obsessive-compulsive disorder, Schizophrenia, Tourette syndrome

519
Myelin associated oligodendrocyte basic protein
-
Alzheimer disease, Amyotrophic lateral sclerosis, Attention deficit hyperactivity disorder, Corticobasal degeneration, Frontotemporal dementia, Progressive supranuclear palsy, Schizophrenia

520
Molybdenum cofactor sulfurase
HMCS, MCS, MOS
Autism, Bipolar disorder, Major depressive disorder, Pancytopenia, Hyperoxaluria, Schizophrenia, Vasculitis, Xanthinuria