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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

Search results for "pentosyltransferase activity"

Displaying entries **76 - 100** of **9011** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
72962	thymidine phosphorylase	Tymp	Mus musculus (house mouse)	cervical squamous cell carcinoma common bile duct neoplasm ductal carcinoma in situ endometrial cancer gallbladder carcinoma lung non-small cell carcinoma mitochondrial DNA depletion syndrome 1 mitochondrial encephalomyopathy ovarian cancer pancreatic cancer pancreatic ductal carcinoma renal cell carcinoma seminoma teratoma transitional cell carcinoma urinary bladder cancer
74493	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase 2	Tnks2	Mus musculus (house mouse)
75387	sirtuin 4	Sirt4	Mus musculus (house mouse)	metabolic dysfunction-associated steatotic liver disease
76654	uridine phosphorylase 2	Upp2	Mus musculus (house mouse)
78781	zinc finger CCCH type, antiviral 1	Zc3hav1	Mus musculus (house mouse)
79070	protein O-glucosyltransferase 2	POGLUT2 Aliases: EP58 MGC5302	Homo sapiens (human)	bipolar disorder
79120	ADP-ribosylation factor 4	Arf4	Rattus norvegicus (Norway rat)
79668	poly(ADP-ribose) polymerase family member 8	PARP8 Aliases: ARTD16 FLJ21308 pART16	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer
79691	queuine tRNA-ribosyltransferase accessory subunit 2	QTRT2 Aliases: FLJ12960	Homo sapiens (human)
80285	poly (ADP-ribose) polymerase family, member 9	Parp9	Mus musculus (house mouse)
80351	tankyrase 2	TNKS2 Aliases: ARTD6 PARP-5b PARP-5c PARP5B PARP5C TANK2 TNKL TRF1-interacting ankyrin-related ADP-ribose polymerase 2 pART6	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adenocarcinoma adenoma basal cell carcinoma bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer childhood osteosarcoma cleft lip cribriform carcinoma depressive disorder diabetes mellitus endometrial cancer endometrial carcinoma granular cell carcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder melancholic depression neurotic disorder obsolete melancholia osteosarcoma skin benign neoplasm skin cancer squamous cell carcinoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus uterine corpus cancer
81890	queuine tRNA-ribosyltransferase catalytic subunit 1	QTRT1 Aliases: TGT tRNA-guanine transglycosylase	Homo sapiens (human)	IgA glomerulonephritis acute pancreatitis breast cancer bronchus cancer bronchus carcinoma cancer carcinoma cerebral infarction cerebrovascular disease essential thrombocythemia functionless pituitary adenoma hepatocellular carcinoma liver angiosarcoma liver cancer lung benign neoplasm lung cancer lung carcinoma multiple sclerosis myotonic dystrophy type 2 pancreatitis parapsoriasis parietal foramina prolactinoma psoriasis pulmonary embolism pustulosis of palm and sole sarcomatoid carcinoma split hand-foot malformation 1 split hand-foot malformation 2 split hand-foot malformation 3 split hand-foot malformation 4 split hand-foot malformation 5 split hand-foot malformation 6 split hand-foot malformation
83666	poly(ADP-ribose) polymerase family member 9	PARP9 Aliases: ARTD9 BAL BAL1	Homo sapiens (human)	B-cell lymphoma Bloch-Sulzberger syndrome Gilles de la Tourette syndrome Goodpasture syndrome Loeffler syndrome Richter's syndrome Takayasu's arteritis X-linked chronic granulomatous disease acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia adult acute lymphocytic leukemia adult lymphoma adult respiratory distress syndrome agranulocytosis alcohol dependence alcohol use disorder allergic asthma anorexia nervosa asthma autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bacterial infectious disease bipolar disorder brain disease breast cancer breast carcinoma bronchiectasis cancer central nervous system lymphoma childhood acute lymphocytic leukemia childhood lymphoma chronic granulomatous disease chronic lymphocytic leukemia chronic obstructive pulmonary disease complement deficiency cutaneous porphyria cystic fibrosis diffuse large B-cell lymphoma embryoma eosinophilic pneumonia epithelioid sarcoma erythropoietic protoporphyria extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue extrinsic allergic alveolitis farmer's lung gastric lymphoma giardiasis granulomatosis with polyangiitis hepatitis hepatocellular carcinoma heroin dependence hypereosinophilic syndrome hypomelanosis of Ito idiopathic interstitial pneumonia idiopathic pulmonary fibrosis influenza interstitial lung disease intrinsic asthma leukopenia liver cancer lung disease lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 morphine dependence neutropenia newborn respiratory distress syndrome obesity obsolete ymphosarcoma opiate dependence pneumocystosis pneumonia polyarteritis nodosa postinflammatory pulmonary fibrosis primary ciliary dyskinesia 1 primary ciliary dyskinesia prostate cancer prostate carcinoma pulmonary alveolar proteinosis pulmonary eosinophilia pulmonary fibrosis pulmonary sarcoidosis pulmonary tuberculosis red-green color blindness rheumatoid arthritis sarcoidosis sarcoma schizophrenia scleroderma severe congenital neutropenia spindle cell sarcoma substance abuse substance-related disorder systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic scleroderma tuberculosis tuberculous pneumothorax uveoparotid fever
84875	poly(ADP-ribose) polymerase family member 10	PARP10 Aliases: ARTD10 FLJ14464	Homo sapiens (human)	ataxia telangiectasia bipolar I disorder bipolar disorder hepatocellular carcinoma liver cancer neurodegenerative disease pancreatic cancer pancreatic carcinoma
99929	TCDD-inducible poly(ADP-ribose) polymerase	Tiparp	Mus musculus (house mouse)
101187	poly (ADP-ribose) polymerase family, member 11	Parp11	Mus musculus (house mouse)
106248	queuine tRNA-ribosyltransferase accessory subunit 2	Qtrt2	Mus musculus (house mouse)
109978	ADP-ribosyltransferase 4	Art4	Mus musculus (house mouse)
109979	ADP-ribosyltransferase 3	Art3	Mus musculus (house mouse)
116969	ADP-ribosyltransferase 5	ART5 Aliases: ARTC5	Homo sapiens (human)	cholera
117544	phosphoribosyl pyrophosphate amidotransferase	Ppat	Rattus norvegicus (Norway rat)	hepatocellular carcinoma renal cell carcinoma
120071	LARGE xylosyl- and glucuronyltransferase 2	LARGE2 Aliases: FLJ35207 PP5656	Homo sapiens (human)	Duchenne muscular dystrophy acute myocardial infarction autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy cancer congenital muscular dystrophy coronary thrombosis distal myopathy embryoma facioscapulohumeral muscular dystrophy limb-girdle muscular dystrophy muscular dystrophy myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy prostate cancer prostate carcinoma rippling muscle disease 2 silent myocardial infarction transitional cell carcinoma
143888	protein O-glucosyltransferase 3	POGLUT3 Aliases: MGC33424	Homo sapiens (human)	chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma myofibroma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma uterine fibroid
144811	laccase domain containing 1	LACC1 Aliases: FAMIN FLJ38725 fatty acid metabolism–immunity nexus	Homo sapiens (human)	Crohn's colitis Crohn's disease anterior uveitis arthritis arthropathy exanthem inflammatory bowel disease 1 inflammatory bowel disease juvenile rheumatoid arthritis pericarditis ulcerative colitis
151531	uridine phosphorylase 2	UPP2 Aliases: UDRPASE2 UP2 UPASE2	Homo sapiens (human)	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

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