Genes | GeDiPNet - Gene Disease Pathway & Associations

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All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

7691 to 7700 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
7691	79892	MCMBP	Minichromosome maintenance complex binding protein	C10orf119, MCM-BP	Major depressive disorder
7692	157777	MCMDC2	Minichromosome maintenance domain containing 2	C8orf45	Azoospermia, Male infertility single gene azoospermia
7693	57192	MCOLN1	Mucolipin TRP cation channel 1	LECD, MG-2, ML1, ML4, MLIV, MST080, MSTP080, TRP-ML1, TRPM-L1, TRPML1	Brainstem atrophy, Congenital neurologic anomalies, Corneal dystrophy, Intellectual developmental disorder, Kidney failure, Mucolipidosis, Spastic paraplegia
7694	79648	MCPH1	Microcephalin 1	BRIT1, MCT	Atherosclerosis, Primary microcephaly, Color vision deficiency, Congenital microcephaly, Congenital neurologic anomalies, Dental caries, Global developmental delay, Hereditary breast cancer, Intellectual developmental disorder, Kidney cancer, Lymphatic malformation, Microcephaly, Open angle glaucoma
7695	348262	MCRIP1	MAPK regulated corepressor interacting protein 1	FAM195B, GRAN2, MCRIP	Systemic lupus erythematosus
7696	84331	MCRIP2	MAPK regulated corepressor interacting protein 2	C16orf14, FAM195A, c349E10.1	Insomnia
7697	10445	MCRS1	Microspherule protein 1	ICP22BP, INO80Q, MCRS2, MSP58, P78	Schizophrenia
7698	79772	MCTP1	Multiple C2 and transmembrane domain containing 1	-	Anorexia nervosa, Attention deficit hyperactivity disorder, Bipolar disorder, Breast cancer, Eating disorder, Head and neck neoplasm, Hypertrophic cardiomyopathy, Keratoconus, Metabolic syndrome, Multiple sclerosis, Neuromuscular disease, Peripheral arterial disease, Substance abuse, Diabetes mellitus type 2
7699	55784	MCTP2	Multiple C2 and transmembrane domain containing 2	-	Alzheimer disease, Attention deficit hyperactivity disorder, Congenital heart disease, Coronary artery disease, Dementia, Chromosome 15q deletion syndrome, Major depressive disorder, Nephrolithiasis, Parkinson disease, Schizophrenia, Tetralogy of fallot, Depression
7700	28985	MCTS1	MCTS1 re-initiation and release factor	IMD118, MCT-1, MCT1	Immunodeficiency

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