Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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7961 to 7970 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7961
MAX network transcriptional repressor
MAD6, MXD6, ROX, bHLHd3, lncRNA-HAL
Lissencephaly, Cleft palate, Craniofacial abnormalities, Insomnia, Diabetes mellitus type 2

7962
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

7963
Modulator of apoptosis 1
MAP-1, PNMA4
Endometriosis, Gout

7964
MOB kinase activator 1A
C2orf6, MABKL1B, MATS1, MOB1, MOBK1B, MOBKL1B, Mob4B
Alzheimer disease

7965
MOB kinase activator 1B
MATS2, MOB4A, MOBKL1A
Alzheimer disease, Atrial fibrillation, Kidney disease, Diabetes mellitus, Kidney failure, Diabetes mellitus type 2

7966
MOB kinase activator 2
HCCA2
Diverticular disease, Prostate cancer

7967
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

7968
MOB kinase activator 3C
MOB1E, MOBKL2C
Kidney disease, Hypertension, Sinusitis

7969
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

7970
Myelin associated oligodendrocyte basic protein
-
Alzheimer disease, Amyotrophic lateral sclerosis, Attention deficit hyperactivity disorder, Corticobasal degeneration, Frontotemporal dementia, Progressive supranuclear palsy, Schizophrenia