Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "M"

511 to 520 of 971 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
511	4327	MMP19	Matrix metallopeptidase 19	CODA, MMP18, RASI-1	Cavitary optic disc anomalies, Miscarriage
512	4330	MN1	MN1 proto-oncogene, transcriptional regulator	CEBALID, MGCR, MGCR1, MGCR1-PEN, dJ353E16.2	Breast carcinoma, Chordoma, Craniosynostosis, Developmental delay, Dysmorphic features, Leukemia, Meningioma, Mental retardation, Multiple congenital anomalies, Multiple meningioma, Myeloid leukemia, Polymicrogyria
513	4335	MNT	MAX network transcriptional repressor	MAD6, MXD6, ROX, bHLHd3, lncRNA-HAL	Lissencephaly, Lissencephaly, x-linked, Classical lissencephalies and subcortical band heterotopias, Miller dieker syndrome, Subcortical band heterotopia
514	4336	MOBP	Myelin associated oligodendrocyte basic protein	-	Alzheimer disease, Amyotrophic lateral sclerosis, Amyotrophic lateral sclerosis with dementia, Attention deficit hyperactivity disorder, Corticobasal degeneration, Lateral sclerosis, Non-obstructive azoospermia, Progressive supranuclear ophthalmoplegia, Progressive supranuclear palsy, Supranuclear palsy
515	4337	MOCS1	Molybdenum cofactor synthesis 1	MIG11, MOCOD, MOCS1A, MOCS1B	Cerebral atrophy, Combined molybdoflavoprotein enzyme deficiency, Deficiency of aldehyde oxidase, Frontal bossing, Hypoplasia of corpus callosum, Macrocephaly, Mental retardation, Microcephaly, Molybdenum cofactor deficiency, Nystagmus, Spastic quadriplegia, Spastic tetraparesis, Sulfite oxidase deficiency, Xanthinuria
516	4338	MOCS2	Molybdenum cofactor synthesis 2	MCBPE, MOCO1, MOCODB, MPTS	Cerebral atrophy, Combined molybdoflavoprotein enzyme deficiency, Ectopia lentis, Frontal bossing, Hypoplasia of corpus callosum, Macrocephaly, Microcephaly, Molybdenum cofactor deficiency, Nystagmus, Spastic quadriplegia, Sulfite oxidase deficiency, Xanthinuria
517	4340	MOG	Myelin oligodendrocyte glycoprotein	BTN6, BTNL11, MOGIG2, NRCLP7	Amnesia, Cataplexy, Demyelinating diseases, Diabetes mellitus, Graves disease, Hallucinations, Narcolepsy, Narcolepsy-cataplexy syndrome, Obesity, Schizophrenia
518	4342	MOS	MOS proto-oncogene, serine/threonine kinase	MSV, OZEMA20	Lung adenocarcinoma
519	4343	MOV10	Mov10 RNA helicase	fSAP113, gb110	Hypertension
520	4351	MPI	Mannose phosphate isomerase	CDG1B, PMI, PMI1	Antithrombin deficiency, Cirrhosis, Congenital disorder of glycosylation, Congenital hepatic fibrosis, Hyperinsulinemic hypoglycemia, Hypoalbuminemia, Hypoglycemia, Liver failure, Liver fibrosis, Malabsorption syndrome, Protein-losing enteropathy

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