GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **6051 - 6075** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
53829	purinergic receptor P2Y13	P2RY13
53831	G protein-coupled receptor 84	GPR84
53832	interleukin 20 receptor subunit alpha	IL20RA
53833	interleukin 20 receptor subunit beta	IL20RB
53834	fibroblast growth factor receptor like 1	FGFRL1
53836	G protein-coupled receptor 87	GPR87
53838	chromosome 11 open reading frame 24	C11orf24
53841	cadherin related family member 5	CDHR5
53905	dual oxidase 1	DUOX1
53918	pelota mRNA surveillance and ribosome rescue factor	PELO
53919	solute carrier organic anion transporter family member 1C1	SLCO1C1
53942	contactin 5	CNTN5 NB-2 hNB-2	Behcet's disease Hirschsprung's disease Parkinson's disease 2 anorexia nervosa atrial fibrillation attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bipolar disorder communicating hydrocephalus congestive heart failure depressive disorder differentiated thyroid gland carcinoma essential hypertension gout hydrocephalus hypertension major depressive disorder melancholic depression neurotic disorder obsolete melancholia obstructive hydrocephalus primary biliary cholangitis schizophrenia senile degeneration of brain
53947	alpha 1,4-galactosyltransferase (P1PK blood group)	A4GALT A14GALT CD77 synthase Gb3 synthase Gb3S P(k) globotriaosylceramide synthase lactosylceramide 4-alpha-galactosyltransferase	Burkitt lymphoma Caffey disease acute megakaryocytic leukemia adenocarcinoma adenoma cancer cribriform carcinoma embryoma gastric adenocarcinoma granular cell carcinoma hematologic cancer hemolytic-uremic syndrome kidney failure leukemia teratocarcinoma thrombophilia tubular adenocarcinoma
53981	cleavage and polyadenylation specific factor 2	CPSF2
54014	bromodomain and WD repeat domain containing 1	BRWD1
54020	solute carrier family 37 member 1	SLC37A1
54069	MIS18 kinetochore protein A	MIS18A
54084	thrombospondin type laminin G domain and EAR repeats	TSPEAR
54097	FAM3 metabolism regulating signaling molecule B	FAM3B
54106	toll like receptor 9	TLR9
54107	DNA polymerase epsilon 3, accessory subunit	POLE3
54112	G protein-coupled receptor 88	GPR88
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
54206	ERBB receptor feedback inhibitor 1	ERRFI1	endometrial cancer osteoarthritis
54207	potassium two pore domain channel subfamily K member 10	KCNK10

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