GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (9988) Glycans (5831) Glycoproteins (15733) Lectins (298) Pathways (2074)

Displaying entries **3951 - 3975** of **9988** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
4326	matrix metallopeptidase 17	MMP17 MT4-MMP	adenocarcinoma adenoma aortic aneurysm arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis breast adenocarcinoma breast cancer breast carcinoma cancer coronary artery disease cribriform carcinoma embryoma granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma migraine osteoporosis rheumatoid arthritis tubular adenocarcinoma
4325	matrix metallopeptidase 16	MMP16
4324	matrix metallopeptidase 15	MMP15
4323	matrix metallopeptidase 14	MMP14
4322	matrix metallopeptidase 13	MMP13
4321	matrix metallopeptidase 12	MMP12
4312	matrix metallopeptidase 1	MMP1
56955	matrix extracellular phosphoglycoprotein	MEPE
9782	matrin 3	MATR3
8785	matrilin 4	MATN4
4148	matrilin 3	MATN3
4147	matrilin 2	MATN2
4146	matrilin 1	MATN1
9833	maternal embryonic leucine zipper kinase	MELK
55534	mastermind like transcriptional coactivator 3	MAML3
84441	mastermind like transcriptional coactivator 2	MAML2
9794	mastermind like transcriptional coactivator 1	MAML1
10046	mastermind like domain containing 1	MAMLD1
284021	mast cell immunoglobulin like receptor 1	MILR1
199675	mast cell expressed membrane protein 1	MCEMP1
4288	marker of proliferation Ki-67	MKI67
7841	mannosyl-oligosaccharide glucosidase	MOGS CWH41 DER7 GCS1 glucosidase I processing A-glucosidase I	Japanese encephalitis Turner syndrome Zika fever acquired hyperkeratosis actinic keratosis acute lymphoblastic leukemia acute myeloid leukemia adamantinoma agammaglobulinemia ameloblastoma blepharophimosis bronchus cancer bronchus carcinoma cancer cerebral degeneration chronic monocytic leukemia chronic myelomonocytic leukemia congenital disorder of glycosylation In congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital disorder of glycosylation type II congenital disorder of glycosylation type IIb congenital disorder of glycosylation cystic fibrosis dengue disease epilepsy gonadal dysgenesis holoprosencephaly 1 holoprosencephaly juvenile myelomonocytic leukemia keratoacanthoma lung benign neoplasm lung cancer lung carcinoma lymphoblastic lymphoma malaria melanoma obesity optic atrophy pleomorphic xanthoastrocytoma sensorineural hearing loss skin melanoma viral infectious disease visual epilepsy yellow fever
149175	mannosidase endo-alpha like	MANEAL FLJ31434	alternating hemiplegia of childhood autonomic neuropathy central nervous system disease nervous system disease neurodegenerative disease
79694	mannosidase endo-alpha	MANEA FLJ12838 endomannosidase glycoprotein endo-alpha-1,2-mannosidase mandaselin	anxiety disorder autoimmune disease autoimmune lymphoproliferative syndrome breast cancer cancer cocaine abuse cocaine dependence delusional disorder disease of mental health embryoma endocarditis immune system disease infective endocarditis morphine dependence panic disorder paranoid schizophrenia phobic disorder polycystic ovary syndrome psychotic disorder social phobia subacute bacterial endocarditis
4126	mannosidase beta	MANBA beta-mannosidase A	Fabry disease allergic asthma allergic disease alternating hemiplegia of childhood angiokeratoma ascending cholangitis asthma attention deficit hyperactivity disorder autonomic neuropathy beta-mannosidosis central nervous system disease cholangitis chronic kidney disease chylomicron retention disease colorectal cancer colorectal carcinoma complement deficiency congenital nystagmus dissociated nystagmus epilepsy intellectual disability intrinsic asthma large intestine cancer learning disability lipid storage disease lysosomal storage disease multiple sclerosis nervous system disease obsolete constipation pathologic nystagmus primary biliary cholangitis primary sclerosing cholangitis sarcoidosis sclerosing cholangitis sensorineural hearing loss speech disorder spontaneous ocular nystagmus suppurative cholangitis uveoparotid fever visual epilepsy

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