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"
331 to 340 of 898 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

331
Meteorin, glial cell differentiation regulator
C16orf23, c380A1.2
Ankylosing spondylitis, Atrial fibrillation, Insomnia

332
Meteorin like, glial cell differentiation regulator
-
Neoplasms, Breast cancer, Cataract, Colorectal adenoma, Colorectal cancer, Diabetes mellitus type 2, Liver cirrhosis, Migraine

333
Methyltransferase 1, tRNA methylguanosine
C12orf1, TRM8, TRMT8, YDL201w
Cortical development malformation, Multiple sclerosis

334
Methyltransferase 13, eEF1A N-terminus and K55
5630401D24Rik, CGI-01, DFNB26, DFNB26M, DFNM1, EEF1AKNMT, KIAA0859, feat
Astrocytoma, Attention deficit hyperactivity disorder, Autism, Deafness, Parkinson disease

335
Methyltransferase 14, N6-adenosine-methyltransferase non-catalytic subunit
hMETTL14
Cardiomyopathy, Edema, Diabetes mellitus type 2, Multiple myeloma, Necrosis, Ventricular dysfunction

336
Methyltransferase 15, mitochondrial 12S rRNA N4-cytidine
METT5D1
Anxiety disorder, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Cannabis abuse, Lymphocytic leukemia, Major depressive disorder, Neurotic disorder, Obesity, Obsessive-compulsive disorder, Obstructive sleep apnea syndrome, Open angle glaucoma, Osteoarthritis, Post-traumatic stress disorder, Psychiatric disorders
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337
Methyltransferase 16, RNA N6-adenosine
METT10D
Central nervous system cancer, Glioblastoma, Glioma, Insomnia, Diabetes mellitus type 2

338
Methyltransferase 21A, HSPA lysine
FAM119A, HCA557b, HSPA-KMT
Schizophrenia, Amyotrophic lateral sclerosis

339
Methyltransferase 21C, AARS1 lysine
C13orf39
Color vision deficiency

340
Methyltransferase 22, Kin17 lysine
C16orf68
Systemic scleroderma