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"
351 to 360 of 898 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

351
Methyltransferase 9, His-X-His N1(pi)-histidine
CGI-81, DREV, DREV1, PAP1, hMETTL9
Androgenetic alopecia, Bipolar disorder, Major depressive disorder, Schizophrenia, Scoliosis

352
Mex-3 RNA binding family member A
MEX-3A, RKHD4, RNF162
Basal cell carcinoma

353
Mex-3 RNA binding family member B
MEX-3B, RKHD3, RNF195
Otosclerosis, Sensory peripheral neuropathy

354
Mex-3 RNA binding family member C
BM-013, MEX-3C, RKHD2, RNF194
Juvenile arthritis, Atrial fibrillation, Cardiovascular disease, Hypertension, Insomnia, Juvenile idiopathic arthritis, Oligoarticular juvenile idiopathic arthritis

355
Microfibril associated protein 2
MAGP, MAGP-1, MAGP1
Obstructive pulmonary disease, Gastroesophageal reflux disease, Ovarian cysts

356
Microfibril associated protein 3
-
Metabolic syndrome, Obesity, Schizophrenia, Diabetes mellitus type 2

357
Microfibril associated protein 3 like
NYD-sp9
Anxiety disorder, Dementia, Major depressive disorder

358
Microfibril associated protein 4
-
Liver cirrhosis

359
Microfibril associated protein 5
AAT9, MAGP-2, MAGP2, MFAP-5, MP25
Aortic aneurysm, Cataract, Congenital contractural arachnodactyly, Connective tissue disease, Thoracic aortic aneurysm and aortic dissection, Hypertension, Marfan syndrome, Migraine, Diabetes mellitus type 2

360
Mitochondrial fission factor
C2orf33, EMPF2, GL004
Exostoses, Global developmental delay, Leigh syndrome, Mitochondrial encephalomyopathy, Myocardial infarction, Ventricular dysfunction