Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "M"
241 to 250 of 971 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

241
MORC family CW-type zinc finger 1
CT33, MORC, ZCW6
Alzheimer disease, Attention deficit hyperactivity disorder, Colorectal cancer, Major depressive disorder, Substance abuse, Depression

242
Metabolism of cobalamin associated D
C2orf25, CL25022, HMAD, MACD, MAHCD, cblD
Acute lymphoblastic leukemia, Cobalamin c disease, Homocystinuria with megaloblastic anemia, Methylmalonic acidemia, Vitamin d deficiency

243
Malonyl-CoA-acyl carrier protein transacylase
FASN2C, MCT, MCT1, MT, NET62, OPA15, fabD
Optic atrophy, Schizophrenia

244
Myosin IH
CCHS2
Bipolar disorder, Haddad syndrome, Central hypoventilation syndrome, Color vision deficiency, Congenital central hypoventilation syndrome, Insomnia, Major depressive disorder, Migraine, Mood disorder, Neurotic disorder, Schizophrenia

245
Mucin 19, oligomeric (gene/pseudogene)
MUC-19
Alzheimer disease, Astrocytoma, Central nervous system cancer, Crohn disease, Glioma, Inflammatory bowel disease, Obesity, Parkinson disease, Sclerosing cholangitis, Ulcerative colitis

246
MEF2 activating motif and SAP domain containing transcriptional regulator
MASTR
Alzheimer disease, Breast cancer, Cholecystolithiasis, Rhinosinusitis, Colorectal cancer, Crohn disease, Dental caries, Hyperlipidemia, Gastroesophageal reflux disease, Inflammatory bowel disease, Multiple sclerosis, Nasal disorder, Osteoarthritis, Sinusitis, Ulcerative colitis
View all (2 more)

247
Melanin concentrating hormone receptor 1
GPR24, MCH-1R, MCH1R, SLC-1, SLC1
Bipolar disorder, Colorectal cancer, Major depressive disorder, Insomnia, Large artery stroke, Depression, Mood disorder, Obesity, Neurotic disorder, Schizophrenia

248
MIR646 host gene
C20orf197, LINC02910

249
Mitochondrial ribosomal protein S28
COXPD47, HSPC007, MRP-S28, MRP-S35, MRPS35
Breast neoplasm, Combined oxidative phosphorylation deficiency, Mitochondrial disease

250
Mitochondrial ribosomal protein S18B
C6orf14, HSPC183, HumanS18a, MRP-S18-2, MRPS18-2, PTD017, S18amt, mS40
Neuroblastoma, Psoriatic arthritis, Stomach neoplasms