GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **5126 - 5150** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
113230	MISP family member 3	MISP3
4286	melanocyte inducing transcription factor	MITF
4288	marker of proliferation Ki-67	MKI67
23608	makorin ring finger protein 1	MKRN1
23609	makorin ring finger protein 2	MKRN2
9761	malectin	MLEC oligosaccharyltransferase complex subunit (non-catalytic)
4292	mutL homolog 1	MLH1
90523	muscular LMNA interacting protein	MLIP
197259	mixed lineage kinase domain like pseudokinase	MLKL
4298	MLLT1 super elongation complex subunit	MLLT1
8028	MLLT10 histone lysine methyltransferase DOT1L cofactor	MLLT10
4300	MLLT3 super elongation complex subunit	MLLT3
4302	MLLT6, PHD finger containing	MLLT6
2862	motilin receptor	MLNR
22877	MLX interacting protein	MLXIP
51085	MLX interacting protein like	MLXIPL
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
326625	metabolism of cobalamin associated B	MMAB
4311	membrane metalloendopeptidase	MME
79258	membrane metalloendopeptidase like 1	MMEL1
93380	membrane magnesium transporter 1	MMGT1
4312	matrix metallopeptidase 1	MMP1
4321	matrix metallopeptidase 12	MMP12
4322	matrix metallopeptidase 13	MMP13
4323	matrix metallopeptidase 14	MMP14

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