GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **4826 - 4850** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
4314	matrix metallopeptidase 3	MMP3
79148	matrix metallopeptidase 28	MMP28
64066	matrix metallopeptidase 27	MMP27
56547	matrix metallopeptidase 26	MMP26
64386	matrix metallopeptidase 25	MMP25 MT6-MMP	X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 acoustic neuroma acute pericementitis adult fibrosarcoma aggressive periodontitis amelogenesis imperfecta hypomaturation type 2A2 amelogenesis imperfecta hypomaturation type 2A3 amelogenesis imperfecta hypomaturation type 2A4 amelogenesis imperfecta hypomaturation type 2A5 amelogenesis imperfecta type 1A amelogenesis imperfecta type 1B amelogenesis imperfecta type 1C amelogenesis imperfecta type 1E amelogenesis imperfecta type 1F amelogenesis imperfecta type 1G amelogenesis imperfecta type 1H amelogenesis imperfecta type 2A1 amelogenesis imperfecta type 3A amelogenesis imperfecta type 4 amelogenesis imperfecta anaplastic astrocytoma angiomatous meningioma arthritis arthropathy benign meningioma brain cancer breast cancer breast carcinoma cancer carcinoma cerebral convexity meningioma childhood cerebral astrocytoma clear cell meningioma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer dental fluorosis dentin dysplasia dentinogenesis imperfecta embryoma fibrillary astrocytoma fibrosarcoma fibrous meningioma gemistocytic astrocytoma giant cell glioblastoma glioblastoma in situ carcinoma intraorbital meningioma intraventricular meningioma juvenile pilocytic astrocytoma large intestine cancer laryngeal squamous cell carcinoma malignant astrocytoma melanoma meningioma meningothelial meningioma microcystic meningioma multiple myeloma multiple sclerosis olfactory groove meningioma osteoarthritis parasagittal meningioma periodontosis pilocytic astrocytoma pituitary adenoma protoplasmic astrocytoma psammomatous meningioma rheumatoid arthritis sarcomatoid carcinoma secretory meningioma skin melanoma spinal meningioma stomach cancer stomach carcinoma subependymal giant cell astrocytoma transitional meningioma
8510	matrix metallopeptidase 23B	MMP23B
118856	matrix metallopeptidase 21	MMP21
9313	matrix metallopeptidase 20	MMP20
4313	matrix metallopeptidase 2	MMP2
4327	matrix metallopeptidase 19	MMP19
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
93380	membrane magnesium transporter 1	MMGT1
79258	membrane metalloendopeptidase like 1	MMEL1
4311	membrane metalloendopeptidase	MME
326625	metabolism of cobalamin associated B	MMAB
23417	malonyl-CoA decarboxylase	MLYCD MCD hMCD	Castleman disease Kaposi's sarcoma Kimura disease Laron syndrome Marfan syndrome Meesmann corneal dystrophy Schmid metaphyseal chondrodysplasia Senior-Loken syndrome achondroplasia acquired immunodeficiency syndrome acute kidney tubular necrosis adult lymphoma autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome cancer cardiomyopathy central nervous system lymphoma childhood lymphoma choline deficiency disease diabetes mellitus diarrhea endomyocardial fibrosis epilepsy essential hypertension familial hypertrophic cardiomyopathy familial nephrotic syndrome focal segmental glomerulosclerosis glomerulonephritis human immunodeficiency virus infectious disease hypertension hypertrophic cardiomyopathy hypoglycemia inherited metabolic disorder kidney disease lactic acidosis lipoid nephrosis liver cirrhosis lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 macular corneal dystrophy membranous glomerulonephritis metabolic dysfunction-associated steatotic liver disease microphthalmia multicentric Castleman disease nasopharynx carcinoma nephritis nephronophthisis 1 nephronophthisis nephrosclerosis nephrosis nephrotic syndrome normal pressure hydrocephalus obesity obsolete Matthew-Wood syndrome obsolete constipation obsolete ymphosarcoma oral tuberculosis primary immunodeficiency disease pyoureter situs inversus steatotic liver disease systemic Epstein-Barr virus positive T-cell lymphoma of childhood tuberculosis tuberous sclerosis 1 tuberous sclerosis type 2 diabetes mellitus visual epilepsy
51085	MLX interacting protein like	MLXIPL
22877	MLX interacting protein	MLXIP
2862	motilin receptor	MLNR

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