GlyCosmos Portal

Table Filtering

Gene ID

Gene Name

Gene Symbol

Organism

Taxonomy ID

Disease Ontology

Disease Ontology ID

Gene Ontology

Gene Ontology ID

Display
results per page.

Clear

Submissions

GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	July 8, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **551 - 575** of **662** in total

« First

‹ Prev

…

19

20

21

22

23

24

25

26

27

Next ›

Last »
Gene ID	Gene Name	Gene Symbol	Organism ▼	Disease Ontology
244416	protein phosphatase 1, regulatory subunit 3B	Ppp1r3b	Mus musculus (house mouse)	alcohol use disorder
226041	phosphoglucomutase 5	Pgm5	Mus musculus (house mouse)
18538	proliferating cell nuclear antigen	Pcna	Mus musculus (house mouse)	Lewy body dementia ataxia-telangiectasia-like disorder-2 brain ischemia hepatocellular carcinoma hypothyroidism invasive ductal carcinoma leiomyoma liver cancer mucositis nephroblastoma obstructive jaundice osteoporosis renal cell carcinoma sciatic neuropathy seminoma stomach cancer transient cerebral ischemia
230101	glucosidase beta 2	Gba2	Mus musculus (house mouse)	hereditary spastic paraplegia 46
22228	uncoupling protein 2 (mitochondrial, proton carrier)	Ucp2	Mus musculus (house mouse)	Huntington's disease carotid artery disease congestive heart failure diabetic neuropathy end stage renal disease hypertension hypothyroidism metabolic dysfunction-associated steatotic liver disease obesity obstructive jaundice polycystic liver disease steatotic liver disease transient cerebral ischemia type 2 diabetes mellitus
18598	pyruvate dehydrogenase E1 alpha 2	Pdha2	Mus musculus (house mouse)	disease of metabolism pyruvate decarboxylase deficiency retinal degeneration spermatogenic failure
71103	glycosyltransferase 6 domain containing 1	Glt6d1	Mus musculus (house mouse)
330671	beta-1,4-N-acetyl-galactosaminyl transferase 4	B4galnt4	Mus musculus (house mouse)
278279	transmembrane and tetratricopeptide repeat containing 2	Tmtc2	Mus musculus (house mouse)
70893	galactosidase, beta 1 like 3	Glb1l3	Mus musculus (house mouse)
105887	UDP glycosyltransferases 3 family, polypeptide A1	Ugt3a1	Mus musculus (house mouse)
30924	angiopoietin-like 3	Angptl3	Mus musculus (house mouse)	alcohol use disorder familial hypobetalipoproteinemia 2
22239	UDP galactosyltransferase 8A	Ugt8a	Mus musculus (house mouse)
74343	CREB regulated transcription coactivator 2	Crtc2	Mus musculus (house mouse)	type 2 diabetes mellitus
83921	cell migration inducing hyaluronidase 2	Cemip2	Mus musculus (house mouse)
16795	LARGE xylosyl- and glucuronyltransferase 1	Large1	Mus musculus (house mouse)	congenital muscular dystrophy-dystroglycanopathy type A6 facioscapulohumeral muscular dystrophy muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B6
11676	aldolase C, fructose-bisphosphate	Aldoc	Mus musculus (house mouse)	autoimmune disease of the nervous system borna disease hepatocellular carcinoma
27376	solute carrier family 25 (mitochondrial carrier, dicarboxylate transporter), member 10	Slc25a10	Mus musculus (house mouse)	mitochondrial DNA depletion syndrome 19 mitochondrial DNA depletion syndrome mitochondrial complex I deficiency myoclonic-atonic epilepsy
21926	tumor necrosis factor	Tnf	Mus musculus (house mouse)	Alzheimer's disease Behcet's disease COVID-19 Cor pulmonale Crohn's disease Fanconi anemia Gaucher's disease Graves ophthalmopathy Graves' disease IgA glomerulonephritis Kawasaki disease Mycobacterium avium complex disease Mycoplasma pneumoniae pneumonia Plasmodium falciparum malaria Sjogren's syndrome Stevens-Johnson syndrome Vogt-Koyanagi-Harada disease Weill-Marchesani syndrome acne acquired immunodeficiency syndrome acute myocardial infarction adult respiratory distress syndrome alcoholic hepatitis amyloidosis anemia anogenital venereal wart anterior uveitis anti-basement membrane glomerulonephritis aortic valve stenosis aplastic anemia aspiration pneumonia asthma atopic dermatitis atrial fibrillation autistic disorder autoimmune hepatitis bacterial pneumonia beta thalassemia brain infarction breast adenocarcinoma breast cancer bronchiectasis bronchopulmonary dysplasia cardiac arrest cardiomyopathy cerebral infarction cervical cancer cholesteatoma of middle ear chorioamnionitis chronic obstructive pulmonary disease cicatricial pemphigoid cochlear disease congenital diaphragmatic hernia congestive heart failure corneal ulcer coronary artery disease coronary restenosis cryoglobulinemia cystic fibrosis cystitis dermatitis herpetiformis dermatitis diabetic angiopathy diabetic neuropathy diabetic retinopathy dilated cardiomyopathy 1H dilated cardiomyopathy disseminated intravascular coagulation encephalitis end stage renal disease endometriosis endophthalmitis epididymitis epilepsy erythema nodosum esophagitis extrinsic allergic alveolitis eye disease farmer's lung gastritis glaucoma heart valve disease hemochromatosis hepatitis A hepatitis B hepatocellular carcinoma hepatopulmonary syndrome hepatorenal syndrome hereditary hemorrhagic telangiectasia herpes zoster hidradenitis suppurativa high grade glioma human immunodeficiency virus infectious disease hypertension hypochromic microcytic anemia impotence inclusion body myopathy with Paget disease of bone and frontotemporal dementia inflammatory bowel disease intermediate uveitis intracranial aneurysm iron deficiency anemia keratoconjunctivitis sicca kidney disease leprosy liver cirrhosis liver disease low tension glaucoma lung disease lung non-small cell carcinoma lupus nephritis lymphopenia malaria metabolic dysfunction-associated steatohepatitis metabolic dysfunction-associated steatotic liver disease mevalonic aciduria middle cerebral artery infarction migraine without aura migraine mixed connective tissue disease mucocutaneous leishmaniasis mucopolysaccharidosis VI multiple myeloma multiple sclerosis muscular dystrophy myelodysplastic syndrome myocardial infarction myositis neutropenia obesity obstructive sleep apnea open-angle glaucoma oral squamous cell carcinoma otitis media ovarian cancer paracoccidioidomycosis peptic esophagitis perinatal necrotizing enterocolitis periodontitis peritonitis periventricular leukomalacia pleurisy portal hypertension pre-eclampsia primary biliary cholangitis primary open angle glaucoma primary sclerosing cholangitis prostate cancer psoriasis psoriatic arthritis pulmonary edema pulmonary fibrosis pulmonary hypertension pulmonary sarcoidosis pulmonary tuberculosis pustulosis of palm and sole radiculopathy renal cell carcinoma renal hypertension retinal detachment rheumatoid arthritis rhinitis root resorption schizophrenia sciatic neuropathy scleritis sensorineural hearing loss severe acute respiratory syndrome sickle cell anemia silicosis skin disease small cell carcinoma spondyloarthropathy status epilepticus systemic lupus erythematosus thalassemia thrombocytopenia toxic shock syndrome trachoma transient cerebral ischemia tuberculosis type 1 diabetes mellitus type 2 diabetes mellitus typhoid fever ulcerative colitis ureteral obstruction uveitis vascular dementia visceral leishmaniasis visual epilepsy vitiligo
107227	mono-ADP ribosylhydrolase 1	Macrod1	Mus musculus (house mouse)
17448	malate dehydrogenase 2, NAD (mitochondrial)	Mdh2	Mus musculus (house mouse)	brain ischemia congestive heart failure developmental and epileptic encephalopathy 51 myocardial infarction
68292	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	Stt3b	Mus musculus (house mouse)	congenital disorder of glycosylation Iw congenital disorder of glycosylation Ix
14343	fucosyltransferase 1	Fut1	Mus musculus (house mouse)
74241	chondroitin polymerizing factor	Chpf	Mus musculus (house mouse)
16177	interleukin 1 receptor, type I	Il1r1	Mus musculus (house mouse)	COVID-19 cholesteatoma of middle ear chronic recurrent multifocal osteomyelitis pulpitis severe acute respiratory syndrome systemic scleroderma type 1 diabetes mellitus

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements