Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "M"

661 to 670 of 893 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
661	245802	MS4A6E	Membrane spanning 4-domains A6E	-	Alzheimer disease, Hypertrophic cardiomyopathy
662	345222	MSANTD1	Myb/SANT DNA binding domain containing 1	C4orf44	Alzheimer disease, Myocardial infarction, Schizophrenia
663	100526694	MSANTD3-TMEFF1	MSANTD3-TMEFF1 readthrough	C9orf2, C9orf3-TMEFF1, C9orf30-TMEFF1, H7365, TMEFF1, TR-1	Peripheral arterial disease, Squamous cell carcinoma
664	9242	MSC	Musculin	ABF-1, ABF1, MYOR, bHLHa22	Kidney failure
665	343930	MSGN1	Mesogenin 1	MSOG, pMsgn1	Benign prostatic hyperplasia, Renal cell carcinoma, Colorectal adenoma, Schizophrenia, Skeletal dysplasia
666	4436	MSH2	MutS homolog 2	COCA1, FCC1, HNPCC, HNPCC1, LCFS2, LYNCH1, MMRCS2, MSH-2, hMSH2	Alzheimer disease, Lynch syndrome, Colorectal neoplasms, Congenital adrenal hyperplasia, Constitutional mismatch repair deficiency syndrome, Diverticular disease, Hereditary breast cancer, Hypertension, Pancreatic neoplasms, Constitutional mismatch repair deficiency, Muir-torre syndrome, Ovarian cancer, Ovarian cysts, Ovarian neoplasms, Prostate cancer View all (3 more)
667	4437	MSH3	MutS homolog 3	DUP, FAP4, MRP1	Central nervous system cancer, Endometrial cancer, Endometrial neoplasms, Adenomatous polyposis, Glioblastoma, Glioma, Huntington disease, Lynch syndrome, Prostatic neoplasms
668	4438	MSH4	MutS homolog 4	ASG, POF20, SPGF2	Gonadal dysgenesis, Premature ovarian failure, Spermatogenic failure, Testicular azoospermia
669	4439	MSH5	MutS homolog 5	G7, MUTSH5, NG23, POF13, SPGF74	Anxiety disorder, Autism, Azoospermia, Breast cancer, Hepatocellular carcinoma, Common variable immunodeficiency, Head and neck cancer, Hypothyroidism, Irritable bowel syndrome, Lung cancer, Major depressive disorder, Male infertility single gene azoospermia, Mastocytosis, Neurotic disorder, Non-small cell lung carcinoma View all (11 more)
670	2956	MSH6	MutS homolog 6	GTBP, GTMBP, HNPCC5, HSAP, LYNCH5, MMRCS3, MSH-6, p160	Alzheimer disease, Attention deficit hyperactivity disorder, Breast cancer, Color vision deficiency, Lynch syndrome, Colorectal neoplasms, Constitutional mismatch repair deficiency syndrome, Endometrial cancer, Endometrial neoplasms, Gaucher disease, Genetic predisposition to disease, Hereditary breast cancer, Hoarding disorder, Intellectual developmental disorder dysmorphic behavioral, Intracranial hemorrhage View all (10 more)

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