Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "M"

271 to 280 of 893 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
271	51102	MECR	Mitochondrial trans-2-enoyl-CoA reductase	CGI-63, DYTOABG, ETR1, FASN2B, NRBF1, OPA16	Optic atrophy, Childhood-onset dystonia, Childhood-onset dystonia with optic atrophy and basal ganglia abnormalities, Leigh syndrome, Mitochondrial disease, Schizophrenia
272	5469	MED1	Mediator complex subunit 1	CRSP1, CRSP200, DRIP205, DRIP230, PBP, PPARBP, PPARGBP, RB18A, TRAP220, TRIP2	Asthma, Hepatocellular carcinoma, Endometriosis, Systemic lupus erythematosus, Diabetes mellitus type 2
273	84246	MED10	Mediator complex subunit 10	L6, NUT2, TRG20	Colorectal cancer
274	400569	MED11	Mediator complex subunit 11	HSPC296, NDDRSB	Neurodevelopmental disorder
275	9968	MED12	Mediator complex subunit 12	ARC240, CAGH45, FGS1, HDKR, HOPA, Kto, MED12S, OHDOX, OKS, OPA1, TNRC11, TRAP230	Imperforate anus, Blepharophimosis syndrome, Blepharophimosis-intellectual disability syndrome, Breast neoplasms, Dilated cardiomyopathy, Cholestasis-pigmentary retinopathy-cleft palate syndrome, Major depressive disorder, Ehlers-danlos syndrome, Thoracic aortic aneurysm and aortic dissection, Global developmental delay, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Non-organic psychosis, Prostatic neoplasms, Psychotic disorders View all (4 more)
276	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 disorder, Non-specific syndromic intellectual disability, Parkinson disease, Thrombocytopenia
277	9969	MED13	Mediator complex subunit 13	ARC250, DRIP250, HSPC221, MRD61, THRAP1, TRAP240	Alzheimer disease, Autism, Neurodevelopmental disorder, Cortical dysplasia with other brain malformations, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Parkinson disease
278	23389	MED13L	Mediator complex subunit 13L	MRFACD, PROSIT240, THRAP2, TRAP240L	Autism, Breast cancer, Cardiac anomalies - developmental delay - facial dysmorphism syndrome, Central nervous system cancer, Congenital camptodactyly, Congenital heart disease, Corneal astigmatism, Crohn disease, Melanoma, Developmental delay, Developmental delay with facial dysmorphism syndrome, Discordant ventriculoarterial connection, Glioblastoma, Glioma, Global developmental delay View all (9 more)
279	9282	MED14	Mediator complex subunit 14	CRSP150, CRSP2, CSRP, CXorf4, DRIP150, EXLM1, RGR1, TRAP170	Endometriosis, Neurodevelopmental disorder
280	51586	MED15	Mediator complex subunit 15	ARC105, CAG7A, CTG7A, PCQAP, TIG-1, TIG1, TNRC7	Hirschsprung disease, Psoriasis, Schizoaffective disorder, Schizophrenia, Hypertension

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