GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **301 - 325** of **1582** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▼
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
230	aldolase, fructose-bisphosphate C	ALDOC	autoimmune disease of the nervous system borna disease hepatoblastoma hepatocellular carcinoma liver cancer neuroblastoma schizophrenia
5283	phosphatidylinositol glycan anchor biosynthesis class H	PIGH GPI-H phosphatidylinositol N-acetylglucosaminyltransferase subunit H	autistic disorder cancer embryoma epilepsy microcephaly visual epilepsy
8509	N-deacetylase and N-sulfotransferase 2	NDST2 HSST2 NST2	autism spectrum disorder azoospermia intellectual disability prostate cancer prostate carcinoma
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
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
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
4122	mannosidase alpha class 2A member 2	MAN2A2 HsT19662 MANA2X	attention deficit hyperactivity disorder schizophrenia
8704	beta-1,4-galactosyltransferase 2	B4GALT2 Beta-N-acetylglucosaminylglycopeptide beta-1,4-galactosyltransferase N-acetyllactosamine synthase beta4Gal-T2 lactose synthase A	attention deficit hyperactivity disorder cervical cancer colorectal cancer colorectal carcinoma diabetic cataract diabetic retinopathy large intestine cancer
55300	phosphatidylinositol 4-kinase type 2 beta	PI4K2B FLJ11105 PI4KIIB PIK42B	attention deficit hyperactivity disorder bipolar disorder childhood leukemia chronic myeloid leukemia disease of mental health leukemia psychotic disorder schizophrenia
79087	ALG12 alpha-1,6-mannosyltransferase	ALG12 CDG1G ECM39 dol-P-Man dependent alpha-1,6-mannosyltransferase dolichyl-P-Man:Man(7)GlcNAc(2)-PP-dolichol alpha-1,6-mannosyltransferase	atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect clubfoot cone-rod dystrophy congenital disorder of glycosylation Ie congenital disorder of glycosylation Ig congenital disorder of glycosylation type I congenital disorder of glycosylation congestive heart failure cryptorchidism developmental and epileptic encephalopathy 36 fundus albipunctatus hypercalcemia hypospadias nephrocalcinosis patent ductus arteriosus patent foramen ovale phosphorus metabolism disease placental insufficiency polyhydramnios retinal detachment retinitis pigmentosa sensorineural hearing loss
222553	solute carrier family 35 member F1	SLC35F1 dJ230I3.1	atrial fibrillation epilepsy giant cell glioblastoma glioblastoma high grade glioma
22796	component of oligomeric golgi complex 2	COG2	atrial fibrillation cardiovascular system disease congenital disorder of glycosylation type IIq congenital disorder of glycosylation coronary artery disease diabetes mellitus epilepsy familial hypercholesterolemia heart disease hypobetalipoproteinemia locked-in syndrome obsolete constipation quadriplegia rheumatoid arthritis stomach cancer stomach carcinoma type 2 diabetes mellitus visual epilepsy
152002	xyloside xylosyltransferase 1	XXYLT1 FLJ35155	atrial fibrillation bronchus cancer bronchus carcinoma cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma nicotine dependence obesity osteoporosis
283748	phospholipase A2 group IVD	PLA2G4D cPLA2delta	atopic dermatitis dermatitis hepatocellular carcinoma liver cancer mycosis fungoides schizophrenia
79603	ceramide synthase 4	CERS4 FLJ12089 Trh1	atopic dermatitis breast cancer breast carcinoma cancer chronic kidney disease colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma dermatitis embryoma hepatocellular carcinoma large intestine cancer liver cancer liver carcinoma rectal benign neoplasm rectum adenocarcinoma rectum cancer
30814	phospholipase A2 group IIE	PLA2G2E	atopic dermatitis benign mastocytoma dermatitis extracutaneous mastocytoma indolent systemic mastocytosis mast cell neoplasm mastocytosis obesity
165631	poly(ADP-ribose) polymerase family member 15	PARP15 ARTD7 BAL3 FLJ40597 pART7	atherosclerosis cancer depressive disorder embryoma major depressive disorder melancholic depression obsolete melancholia
84875	poly(ADP-ribose) polymerase family member 10	PARP10 ARTD10 FLJ14464	ataxia telangiectasia bipolar I disorder bipolar disorder hepatocellular carcinoma liver cancer neurodegenerative disease pancreatic cancer pancreatic carcinoma
81793	toll like receptor 10	TLR10	asthma
51267	C-type lectin domain family 1 member A	CLEC1A CLEC-1 CLEC1 MGC34328	aspergillosis black piedra coccidioidomycosis histoplasmosis sporotrichosis superficial mycosis white piedra
10333	toll like receptor 6	TLR6	aspergillosis asthma bacterial pneumonia infective endocarditis perinatal necrotizing enterocolitis rhinitis tuberculosis
255189	phospholipase A2 group IVF	PLA2G4F PLA2G4F/Z	arthritis arthropathy osteoarthritis
166012	carbohydrate sulfotransferase 13	CHST13 C4ST3 chondroitin 4-sulfotransferase 3	arthritis arthropathy osteoarthritis primary pulmonary hypertension
197021	lactase like	LCTL FLJ33279 KL lactase phlorizin hydrolase KLG KLPH gammaklotho klotho gamma	arthritis arthropathy kidney disease osteoarthritis

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