GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **276 - 300** of **1582** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▼
64850	ethanolamine-phosphate phospho-lyase	ETNPPL	bipolar disorder borderline personality disorder cancer hepatocellular carcinoma intermittent explosive disorder liver cancer schizophrenia steatotic liver disease
65258	metallophosphoesterase 1	MPPE1 Cdc1 PGAP5 post-GPI attachment to proteins 5	bipolar disorder borderline personality disorder cancer cerebral malaria chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma embryoma hepatitis B hepatitis influenza intermittent explosive disorder malaria melanoma papillary renal cell carcinoma pneumonia renal cell carcinoma sarcomatoid renal cell carcinoma skin melanoma
3613	inositol monophosphatase 2	IMPA2 myo-inositol monophosphatase 2	bipolar disorder borderline personality disorder cancer cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma depressive disorder dysthymic disorder embryoma endometriosis of ovary endometriosis of uterus endometriosis intermittent explosive disorder major depressive disorder melancholic depression mood disorder neurotic disorder nonpapillary renal cell carcinoma obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia
83857	transmembrane O-mannosyltransferase targeting cadherins 1	TMTC1 ARG99 FLJ31400 FLJ41625 OLF	bipolar disorder bone marrow disease colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma disease of mental health endometrial cancer endometrial carcinoma large intestine cancer psychotic disorder schizophrenia spinal cord disease syringomyelia
5467	peroxisome proliferator activated receptor delta	PPARD	biliary tract cancer pancreatic cancer type 2 diabetes mellitus
84869	carbonyl reductase 4	CBR4 FLJ14431 SDR45C1 short chain dehydrogenase/reductase family 45C, member 1	biliary atresia pancreatic cancer tuberculosis
9653	heparan sulfate 2-O-sulfotransferase 1	HS2ST1 KIAA0448	benign mastocytoma extracutaneous mastocytoma hypereosinophilic syndrome indolent systemic mastocytosis mast cell neoplasm mastocytosis melanoma skin melanoma
8372	hyaluronidase 3	HYAL3 LUCA-3 LUCA14 Minna14	basal cell carcinoma cancer carcinoma central nervous system cancer embryoma endometrial cancer endometrial carcinoma glaucoma gliosarcoma high grade glioma lung squamous cell carcinoma mixed glioma sarcomatoid carcinoma uterine corpus cancer
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
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
283417	dpy-19 like 2	DPY19L2 FLJ32949 SPATA34 spermatogenesis associated 34	azoospermia spermatogenic failure 9
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
419	ADP-ribosyltransferase 3 (inactive)	ART3 ARTC3	azoospermia cancer melanoma patent ductus arteriosus skin melanoma steatotic liver disease
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
284541	cytochrome P450 family 4 subfamily A member 22	CYP4A22	autosomal recessive polycystic kidney disease hepatocellular carcinoma hypertension liver cancer polycystic kidney disease 4
84899	transmembrane O-mannosyltransferase targeting cadherins 4	TMTC4 FLJ14624 FLJ22153	autosomal recessive nonsyndromic deafness breast cancer idiopathic scoliosis
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
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
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
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
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
26290	polypeptide N-acetylgalactosaminyltransferase 8	GALNT8 GALNAC-T8 polypeptide GalNAc transferase 8	autosomal dominant hypophosphatemic rickets disease of metabolism hepatitis C
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
54414	sialic acid acetylesterase	SIAE	autoimmune disease
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

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