GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (1582) Glycans (5831) Glycoproteins (18496) Lectins (298) Pathways (2090)

Displaying entries **1151 - 1175** of **1582** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▲
4122	mannosidase alpha class 2A member 2	MAN2A2 HsT19662 MANA2X	attention deficit hyperactivity disorder schizophrenia
9380	glyoxylate and hydroxypyruvate reductase	GRHPR PH2 primary hyperoxaluria type 2	atypical hemolytic-uremic syndrome calcinosis calcium metabolism disease chronic kidney disease hemolytic-uremic syndrome hypercalcemia kidney failure nephrocalcinosis nephrolithiasis phosphorus metabolism disease primary hyperoxaluria type 2 primary hyperoxaluria prostate cancer prostate carcinoma ureteral obstruction uric acid nephrolithiasis urinary tract obstruction
26280	interleukin 1 receptor accessory protein like 2	IL1RAPL2 IL-1R9 IL1R9 IL1RAPL-2 TIGIRR-1	autism spectrum disorder autistic disorder breast cancer childhood type dermatomyositis dermatomyositis hepatitis C myositis
151531	uridine phosphorylase 2	UPP2 UDRPASE2 UP2 UPASE2	autism spectrum disorder autistic disorder cancer depressive disorder diabetes mellitus major depressive disorder melancholic depression obsolete melancholia squamous cell carcinoma tarsal-carpal coalition syndrome tongue squamous cell carcinoma transitional cell carcinoma type 2 diabetes mellitus
8509	N-deacetylase and N-sulfotransferase 2	NDST2 HSST2 NST2	autism spectrum disorder azoospermia intellectual disability prostate cancer prostate carcinoma
5283	phosphatidylinositol glycan anchor biosynthesis class H	PIGH GPI-H phosphatidylinositol N-acetylglucosaminyltransferase subunit H	autistic disorder cancer embryoma epilepsy microcephaly visual epilepsy
230	aldolase, fructose-bisphosphate C	ALDOC	autoimmune disease of the nervous system borna disease hepatoblastoma hepatocellular carcinoma liver cancer neuroblastoma schizophrenia
4124	mannosidase alpha class 2A member 1	MAN2A1 GOLIM7 golgi integral membrane protein 7	autoimmune disease autoimmune lymphoproliferative syndrome cancer childhood acute lymphocytic leukemia congenital dyserythropoietic anemia type II congenital dyserythropoietic anemia diabetes mellitus embryoma giant cell glioblastoma glioblastoma hepatocellular carcinoma high grade glioma immune system disease liver cancer prostate cancer prostate carcinoma schizophrenia systemic lupus erythematosus type 2 diabetes mellitus
2519	alpha-L-fucosidase 2	FUCA2 MGC1314 a-L-fucosidase 2 dJ20N2.5 plasma fucosidase α-L-fucosidase 2	autoimmune disease autoimmune lymphoproliferative syndrome duodenal ulcer glycoproteinosis immune system disease schizophrenia sickle cell anemia
54414	sialic acid acetylesterase	SIAE	autoimmune disease
55304	serine palmitoyltransferase long chain base subunit 3	SPTLC3 FLJ11112 LCB2B hLCB2b	autosomal dominant cerebellar ataxia bacterial sepsis head and neck squamous cell carcinoma hereditary sensory and autonomic neuropathy type 1 neurodegenerative disease neuropathy peripheral nervous system disease polyneuropathy sensory peripheral neuropathy spinocerebellar ataxia type 7
26290	polypeptide N-acetylgalactosaminyltransferase 8	GALNT8 GALNAC-T8 polypeptide GalNAc transferase 8	autosomal dominant hypophosphatemic rickets disease of metabolism hepatitis C
2135	exostosin like glycosyltransferase 2	EXTL2 alpha-1,4-N-acteylhexosaminyltransferase	autosomal dominant osteopetrosis 2 autosomal recessive osteopetrosis 7 cancer chronic kidney disease hereditary multiple exostoses mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIC mucopolysaccharidosis osteopetrosis osteosclerosis
280	amylase alpha 2B	AMY2B	autosomal recessive congenital ichthyosis 1 ichthyosis keratosis follicularis lung benign neoplasm lung carcinoma mongolian spot obsolete congenital ichthyosiform erythroderma pseudoxanthoma elasticum
54936	ADP-ribosylserine hydrolase	ADPRS ADP-ribosylarginine hydrolase like 2 ARH3 FLJ20446	autosomal recessive hypercholesterolemia brain stem infarction breast cancer breast carcinoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease congenital nystagmus congenital ptosis dissociated nystagmus epilepsy hypertropia intellectual disability learning disability mechanical strabismus neurodegenerative disease ophthalmoplegia pathologic nystagmus ptosis spontaneous ocular nystagmus strabismus stress-induced childhood-onset neurodegeneration with variable ataxia and seizures visual epilepsy
141	ADP-ribosylarginine hydrolase	ADPRH ARH1 [Protein ADP-ribosylarginine] hydrolase	autosomal recessive hypercholesterolemia cancer cardiomyopathy cholera endomyocardial fibrosis familial hypercholesterolemia hypertrophic cardiomyopathy ovarian cancer ovarian carcinoma
83548	component of oligomeric golgi complex 3	COG3 SEC34	autosomal recessive limb-girdle muscular dystrophy type 2A breast cancer cancer congenital disorder of glycosylation type II
84899	transmembrane O-mannosyltransferase targeting cadherins 4	TMTC4 FLJ14624 FLJ22153	autosomal recessive nonsyndromic deafness breast cancer idiopathic scoliosis
284541	cytochrome P450 family 4 subfamily A member 22	CYP4A22	autosomal recessive polycystic kidney disease hepatocellular carcinoma hypertension liver cancer polycystic kidney disease 4
9488	phosphatidylinositol glycan anchor biosynthesis class B	PIGB GPI mannosyltransferase 3 GPI-MT-III PIG-B dol-P-Man dependent GPI mannosyltransferase III	axonal neuropathy developmental and epileptic encephalopathy 80 epilepsy intellectual disability learning disability sleeping sickness visual epilepsy
419	ADP-ribosyltransferase 3 (inactive)	ART3 ARTC3	azoospermia cancer melanoma patent ductus arteriosus skin melanoma steatotic liver disease
9651	phospholipase C eta 2	PLCH2 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-2 KIAA0450 PLC-eta2 PLCeta2 RP3-395M20.1	azoospermia intellectual disability learning disability schizophrenia
283417	dpy-19 like 2	DPY19L2 FLJ32949 SPATA34 spermatogenesis associated 34	azoospermia spermatogenic failure 9
730249	aconitate decarboxylase 1	ACOD1 CAD	bacterial sepsis central nervous system cancer gliosarcoma hepatitis B high grade glioma lung disease mixed glioma peripheral artery disease viral infectious disease
5016	oviductal glycoprotein 1	OVGP1 CHIT5 oviductin	bagassosis cancer centronuclear myopathy ciliary body disease colorectal cancer colorectal carcinoma congenital structural myopathy embryoma endometrial carcinoma endosalpingiosis iris disease large intestine cancer laryngitis ovarian cancer ovarian carcinoma panuveitis transient myeloproliferative syndrome tubular aggregate myopathy 1 uveitis

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