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, Diverticular diseases, Mental retardation, Motor delay, Non-syndromic intellectual disability, Platelet-type bleeding disorder
142	118490	MSS51	MSS51 mitochondrial translational activator	ZMYND17	Schizophrenia
143	118856	MMP21	Matrix metallopeptidase 21	HTX7, MMP-21	Asplenia, Atrial isomerism, Atrial septal defect, Benign fibrous histiocytoma, Congenital atresia of pulmonary artery, Congenital malrotation of intestine, Dermatologic disorders, Fibrous histiocytoma, Heterotaxia, Heterotaxy, visceral, Interrupted aortic arch, Interrupted inferior vena cava with azygous continuation, Left atrial isomerism, Polysplenia, Pulmonary venous return anomaly View all (3 more)
144	123263	MTFMT	Mitochondrial methionyl-tRNA formyltransferase	COXPD15, FMT1, MC1DN27	Anemia, Attention deficit hyperactivity disorder, Cerebellar ataxia, Combined oxidative phosphorylation deficiency, Developmental delay, Dysarthria, Hypertrichosis, Hypertrophic cardiomyopathy, Impaired cognition, Mental retardation, Leigh syndrome, Leigh syndrome with leukodystrophy, Leukodystrophy, Mitochondrial complex deficiency, Mitochondrial encephalomyopathy View all (9 more)
145	124512	METTL23	Methyltransferase 23, arginine	C17orf95, MRT44	Absence of septum pellucidum, Autism, Central visual impairment, Cerebral atrophy, Cortical dysplasia, Developmental delay, Dyskinetic syndrome, Dysmorphic features, Dyssomnia, Hypoplasia of corpus callosum, Impaired cognition, Mental retardation, Mental depression, Microcephaly, Motor delay View all (7 more)
146	124540	MSI2	Musashi RNA binding protein 2	MSI2H	Schizophrenia
147	125988	MICOS13	Mitochondrial contact site and cristae organizing system subunit 13	C19orf70, MIC12, MIC13, P117, QIL1	Cerebellar atrophy, Choreoathetosis, Developmental delay, Dysarthria, Hearing loss, Hypoglycemia, Mental retardation, Nystagmus, Optic atrophy, Respiratory failure
148	125997	MBD3L2	Methyl-CpG binding domain protein 3 like 2	-	Gastric cancer, Stomach neoplasms
149	128826	MIR1-1HG	MIR1-1 host gene	C20orf166, MIR133A2HG	Atrial fibrillation, Paroxysmal atrial fibrillation
150	129531	MITD1	Microtubule interacting and trafficking domain containing 1	-	Lipoyltransferase deficiency

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