Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "M"

141 to 150 of 971 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
141	116931	MED12L	Mediator complex subunit 12L	NIZIDS, NOPAR, TNRC11L, TRALP, TRALPUSH	Alzheimer disease, Nonsyndromic intellectual disability, Platelet-type bleeding disorder, Developmental disability, Digestive system disease, Diverticular disease, Insomnia, Intellectual developmental disorder, Irritable bowel syndrome, Neurodevelopmental disorders, Non-specific syndromic intellectual disability, Parkinson disease
142	118490	MSS51	MSS51 mitochondrial translational activator	ZMYND17	Schizophrenia
143	118856	MMP21	Matrix metallopeptidase 21	HTX7, MMP-21	Dermatologic disorder, Heterotaxy syndrome, Situs ambiguus , Situs inversus, Skin disease
144	123263	MTFMT	Mitochondrial methionyl-tRNA formyltransferase	COXPD15, FMT1, MC1DN27	Combined oxidative phosphorylation deficiency, Leigh syndrome, Mitochondrial complex deficiency, Waardenburg syndrome
145	124512	METTL23	Methyltransferase 23, arginine	C17orf95, MRT44	Osteopetrosis, Intellectual developmental disorder
146	124540	MSI2	Musashi RNA binding protein 2	MSI2H	Androgenetic alopecia, Cannabis abuse, Clonal hematopoiesis, Color vision deficiency, Keratitis, Ovarian epithelial cancer, Metabolic syndrome, Open angle glaucoma, Ovarian cancer, Schizophrenia, Diabetes mellitus, type 2
147	125988	MICOS13	Mitochondrial contact site and cristae organizing system subunit 13	C19orf70, MIC12, MIC13, P117, QIL1	3-methylglutaconic aciduria, Combined oxidative phosphorylation deficiency, Mitochondrial disease
148	125997	MBD3L2	Methyl-CpG binding domain protein 3 like 2	-	Stomach neoplasms
149	128826	MIR1-1HG	MIR1-1 host gene	C20orf166, MIR133A2HG
150	129531	MITD1	Microtubule interacting and trafficking domain containing 1	-	Hearing impairment, Lipoyltransferase deficiency

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