GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **3901 - 3925** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
54414	sialic acid acetylesterase	SIAE	autoimmune disease
54413	neuroligin 3	NLGN3
54407	solute carrier family 38 member 2	SLC38A2
54386	TERF2 interacting protein	TERF2IP
54363	hydroxyacid oxidase 1	HAO1 GOX glycolate oxidase 1	familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 hyperinsulinemic hypoglycemia inherited metabolic disorder nephrolithiasis primary hyperoxaluria prostate cancer prostate carcinoma uric acid nephrolithiasis
54361	Wnt family member 4	WNT4
54346	unc-93 homolog A	UNC93A
54344	dolichyl-phosphate mannosyltransferase subunit 3, regulatory	DPM3 DPM synthase complex subunit MGC125904 MGC125905 MGC34275	Duchenne muscular dystrophy autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy cardiomyopathy clubfoot congenital disorder of glycosylation type I congenital muscular dystrophy distal myopathy endomyocardial fibrosis facioscapulohumeral muscular dystrophy hypertrophic cardiomyopathy isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy muscular dystrophy-dystroglycanopathy type B15 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy rippling muscle disease 2
54329	G protein-coupled receptor 85	GPR85
54328	G protein-coupled receptor 173	GPR173
54221	syntrophin gamma 2	SNTG2
54210	triggering receptor expressed on myeloid cells 1	TREM1
54209	triggering receptor expressed on myeloid cells 2	TREM2
54207	potassium two pore domain channel subfamily K member 10	KCNK10
54206	ERBB receptor feedback inhibitor 1	ERRFI1	endometrial cancer osteoarthritis
54187	N-acetylneuraminate synthase	NANS	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 acute myocardial infarction anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation attention deficit hyperactivity disorder bone cancer bone osteosarcoma breast cancer breast carcinoma cancer central nervous system cancer cerebral degeneration cerebral infarction cerebrovascular disease childhood osteosarcoma communicating hydrocephalus congenital central hypoventilation syndrome congenital nystagmus congestive heart failure connective tissue benign neoplasm coronary artery disease coronary thrombosis craniosynostosis depressive disorder diabetes mellitus dissociated nystagmus dysthymic disorder embryoma epilepsy epithelioid sarcoma esophageal cancer esophageal carcinoma essential thrombocythemia generalized anxiety disorder gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma head and neck cancer head and neck squamous cell carcinoma hepatitis B hepatocellular carcinoma high grade glioma hydrocephalus hypertrichosis inflammatory liposarcoma intellectual disability learning disability liposarcoma liver cancer liver cirrhosis major depressive disorder malignant fibrous histiocytoma melancholic depression microcephaly mixed glioma mixed sleep apnea mucopolysaccharidosis IV multiple epiphyseal dysplasia myelodysplastic syndrome myocardial infarction neuroblastoma neurotic disorder obesity obsolete melancholia obstructive hydrocephalus obstructive sleep apnea osteochondrodysplasia osteomyelitis osteosarcoma parapsoriasis pathologic nystagmus peripheral osteosarcoma phobic disorder pleomorphic adenoma pleomorphic liposarcoma polycystic ovary syndrome premenstrual tension prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole restless legs syndrome rhabdomyosarcoma sarcoma sclerosing liposarcoma silent myocardial infarction skin disease sleep apnea social phobia spindle cell sarcoma spondyloepimetaphyseal dysplasia, Genevieve-type spontaneous ocular nystagmus squamous cell carcinoma stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 synovial sarcoma tongue cancer tongue squamous cell carcinoma type 2 diabetes mellitus well-differentiated liposarcoma
54112	G protein-coupled receptor 88	GPR88
54107	DNA polymerase epsilon 3, accessory subunit	POLE3
54106	toll like receptor 9	TLR9
54097	FAM3 metabolism regulating signaling molecule B	FAM3B
54084	thrombospondin type laminin G domain and EAR repeats	TSPEAR
54069	MIS18 kinetochore protein A	MIS18A
54020	solute carrier family 37 member 1	SLC37A1
54014	bromodomain and WD repeat domain containing 1	BRWD1
53981	cleavage and polyadenylation specific factor 2	CPSF2

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