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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

Displaying entries **101 - 125** of **362** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▼
855928	phosphatidylinositol N-acetylglucosaminyltransferase SPT14	SPT14	Saccharomyces cerevisiae S288C	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
855009	lactoylglutathione lyase GLO1	GLO1	Saccharomyces cerevisiae S288C	autistic disorder diabetic retinopathy end stage renal disease type 2 diabetes mellitus vascular disease
850979	protein phosphatase regulator PIG1	PIG1	Saccharomyces cerevisiae S288C	alcohol use disorder type 2 diabetes mellitus
856781	Gip2p	GIP2	Saccharomyces cerevisiae S288C	alcohol use disorder hypoglycemia type 2 diabetes mellitus
854350	protein phosphatase regulator GAC1	GAC1	Saccharomyces cerevisiae S288C	alcohol use disorder hypoglycemia type 2 diabetes mellitus
852051	adenine phosphoribosyltransferase APT2	APT2	Saccharomyces cerevisiae S288C	adenine phosphoribosyltransferase deficiency hepatocellular carcinoma
854986	adenine phosphoribosyltransferase APT1	APT1	Saccharomyces cerevisiae S288C	adenine phosphoribosyltransferase deficiency hepatocellular carcinoma
856294	Rho family GTPase RHO1	RHO1	Saccharomyces cerevisiae S288C	acute myocardial infarction asthma breast cancer breast carcinoma colorectal cancer fetal alcohol syndrome hypertension melanoma membranous glomerulonephritis multiple sclerosis neurodegenerative disease obesity ovarian carcinoma peroxisomal biogenesis disorder pulmonary hypertension ulcerative colitis urinary bladder cancer
851977	putative chitinase	CTS2	Saccharomyces cerevisiae S288C	acute myeloid leukemia arteriosclerosis asthma bacterial meningitis breast cancer bronchopulmonary dysplasia chondrosarcoma chronic obstructive pulmonary disease colorectal carcinoma congestive heart failure coronary artery disease cryptococcosis endometrial cancer glioblastoma hypertension lung non-small cell carcinoma melanoma multiple myeloma myocardial infarction ovarian cancer pre-eclampsia prostate carcinoma pulmonary fibrosis pulmonary sarcoidosis rheumatoid arthritis schizophrenia silicosis sinusitis small cell carcinoma systemic scleroderma temporal arteritis type 1 diabetes mellitus type 2 diabetes mellitus
852546	glutathione peroxidase GPX2	GPX2	Saccharomyces cerevisiae S288C	acute kidney failure colon cancer colorectal adenocarcinoma colorectal cancer gastric adenocarcinoma nephrotic syndrome pre-eclampsia spondylometaphyseal dysplasia Sedaghatian type
853842	glutathione peroxidase GPX1	GPX1	Saccharomyces cerevisiae S288C	acute kidney failure colon cancer colorectal adenocarcinoma colorectal cancer gastric adenocarcinoma nephrotic syndrome pre-eclampsia spondylometaphyseal dysplasia Sedaghatian type
854252	dolichyl-diphosphooligosaccharide--protein glycotransferase OST3	OST3	Saccharomyces cerevisiae S288C	X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia autosomal recessive intellectual developmental disorder 7 bacterial infectious disease congenital disorder of glycosylation Icc primary immunodeficiency disease prostate cancer
854499	dolichyl-phosphate-mannose-protein mannosyltransferase PMT3	PMT3	Saccharomyces cerevisiae S288C	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy congenital muscular dystrophy-dystroglycanopathy type A2 lissencephaly muscular dystrophy-dystroglycanopathy type B2 muscular dystrophy-dystroglycanopathy muscular dystrophy
851210	dolichyl-phosphate-mannose-protein mannosyltransferase PMT2	PMT2	Saccharomyces cerevisiae S288C	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy congenital muscular dystrophy-dystroglycanopathy type A2 lissencephaly muscular dystrophy-dystroglycanopathy type B2 muscular dystrophy-dystroglycanopathy muscular dystrophy
853113	dolichyl-phosphate-mannose-protein mannosyltransferase PMT6	PMT6	Saccharomyces cerevisiae S288C	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy congenital muscular dystrophy-dystroglycanopathy type A2 lissencephaly muscular dystrophy-dystroglycanopathy type B2 muscular dystrophy-dystroglycanopathy muscular dystrophy
853608	dolichyl-phosphate-mannose-protein mannosyltransferase	PMT4	Saccharomyces cerevisiae S288C	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2K cardiomyopathy cleft lip congenital muscular dystrophy-dystroglycanopathy type A1 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy muscular dystrophy
856220	Golgi transport complex subunit COG4	COG4	Saccharomyces cerevisiae S288C	Saul-Wilson syndrome congenital disorder of glycosylation type IIj
853595	mannosyl-oligosaccharide 1,2-alpha-mannosidase	MNS1	Saccharomyces cerevisiae S288C	Rafiq syndrome
855480	glucose-6-phosphate dehydrogenase	ZWF1	Saccharomyces cerevisiae S288C	Plasmodium falciparum malaria anemia cataract cerebrovascular disease cholestasis congenital hypothyroidism congenital nonspherocytic hemolytic anemia diabetes mellitus favism hemolytic anemia hepatic encephalopathy hepatocellular carcinoma hyperhomocysteinemia kidney disease malaria metabolic dysfunction-associated steatotic liver disease myocardial infarction neonatal jaundice obesity phenylketonuria renovascular hypertension transient cerebral ischemia type 1 diabetes mellitus type 2 diabetes mellitus
851013	aconitate hydratase ACO1	ACO1	Saccharomyces cerevisiae S288C	Parkinson's disease central nervous system disease infantile cerebellar-retinal degeneration neurodegenerative disease optic atrophy 9 optic nerve disease
850370	phosphoglycerate kinase	PGK1	Saccharomyces cerevisiae S288C	Parkinson's disease cancer hemolytic anemia phosphoglycerate kinase 1 deficiency
852495	glucose-6-phosphate isomerase	PGI1	Saccharomyces cerevisiae S288C	Parkinson's disease acute lymphoblastic leukemia acute myeloid leukemia congenital hemolytic anemia congenital nonspherocytic hemolytic anemia heart disease intellectual disability neuromuscular disease
856870	type 1 serine/threonine-protein phosphatase catalytic subunit GLC7	GLC7	Saccharomyces cerevisiae S288C	Noonan syndrome-like disorder with loose anagen hair 2 cancer congestive heart failure type 2 diabetes mellitus
850962	glycogen (starch) synthase GSY2	GSY2	Saccharomyces cerevisiae S288C	Lafora disease cardiovascular system disease glycogen storage disease
850569	glycogen (starch) synthase GSY1	GSY1	Saccharomyces cerevisiae S288C	Lafora disease cardiovascular system disease glycogen storage disease

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