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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 **1676 - 1700** of **393515** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▼
180533	Beta-hexosaminidase A	hex-1	Caenorhabditis elegans	Sandhoff disease Tay-Sachs disease lysosomal storage disease spinal muscular atrophy
250735	fused lobes	fdl	Drosophila melanogaster (fruit fly)	Sandhoff disease Tay-Sachs disease lysosomal storage disease spinal muscular atrophy
388512	C-type lectin domain containing 17A	CLEC17A Aliases: FLJ45910 prolectin	Homo sapiens (human)	Richter's syndrome chronic lymphocytic leukemia
946	sialic acid binding Ig like lectin 6	SIGLEC6 Aliases: CD327 OB-BP1 SIGLEC-6	Homo sapiens (human)	Richter's syndrome chronic lymphocytic leukemia colorectal cancer colorectal carcinoma large intestine cancer subacute bacterial endocarditis systemic lupus erythematosus
63917	polypeptide N-acetylgalactosaminyltransferase 11	GALNT11 Aliases: GalNAc-T11 polypeptide GalNAc transferase 11	Homo sapiens (human)	Richter's syndrome cancer chronic lymphocytic leukemia colorectal cancer colorectal carcinoma embryoma idiopathic scoliosis large intestine cancer
3029	hydroxyacylglutathione hydrolase	HAGH Aliases: GLO2 GLXII HAGH1	Homo sapiens (human)	Rett syndrome autism spectrum disorder autistic disorder autosomal dominant polycystic kidney disease cancer carcinoma clear cell adenocarcinoma inflammatory breast carcinoma kidney failure lung cancer lung non-small cell carcinoma polycystic kidney disease 1 prostate cancer prostate carcinoma rheumatoid arthritis sarcomatoid carcinoma schizophrenia uremia
22854	netrin G1	NTNG1 Aliases: KIAA0976 Lmnt1 Netrin-G1 netrin G1f	Homo sapiens (human)	Rett syndrome anorexia nervosa autistic disorder bipolar disorder brain disease cancer cerebral infarction cerebrovascular disease cocaine abuse cocaine dependence colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma epilepsy esophagitis gastroesophageal reflux disease head and neck squamous cell carcinoma hydrocephalus intellectual disability large intestine cancer learning disability lingual-facial-buccal dyskinesia microcephaly morphine dependence movement disease nephrolithiasis neuroendocrine carcinoma neuroendocrine tumor neuropathy patent ductus arteriosus peptic esophagitis peripheral nervous system disease polyneuropathy schizophrenia sensorineural hearing loss uric acid nephrolithiasis visual epilepsy
8789	fructose-bisphosphatase 2	FBP2	Homo sapiens (human)	Rett syndrome X-linked ichthyosis cancer epithelioid sarcoma sarcoma spindle cell sarcoma stomach cancer stomach carcinoma
43436	alpha-Mannosidase class I b	alpha-Man-Ib	Drosophila melanogaster (fruit fly)	Rafiq syndrome
227619	mannosidase, alpha, class 1B, member 1	Man1b1	Mus musculus (house mouse)	Rafiq syndrome
499751	mannosidase, alpha, class 1B, member 1	Man1b1	Rattus norvegicus (Norway rat)	Rafiq syndrome
853595	mannosyl-oligosaccharide 1,2-alpha-mannosidase	MNS1	Saccharomyces cerevisiae S288C	Rafiq syndrome
51738	ghrelin and obestatin prepropeptide	GHRL	Homo sapiens (human)	Prader-Willi syndrome cardiovascular system disease diabetic neuropathy end stage renal disease esophagus adenocarcinoma middle cerebral artery infarction morbid obesity multiple endocrine neoplasia obesity obstructive sleep apnea type 2 diabetes mellitus
14380	glucose-6-phosphate dehydrogenase 2	G6pd2	Mus musculus (house mouse)	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
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
178046	Glucose-6-phosphate 1-dehydrogenase	gspd-1	Caenorhabditis elegans	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
14381	glucose-6-phosphate dehydrogenase X-linked	G6pdx	Mus musculus (house mouse)	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
32974	Zwischenferment	Zw	Drosophila melanogaster (fruit fly)	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
24377	glucose-6-phosphate dehydrogenase	G6pd	Rattus norvegicus (Norway rat)	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
7991	tumor suppressor candidate 3	TUSC3 Aliases: MGC13453 MRT7 MagT2 Magnesium uptake/transporter TUSC3 N33 OST3A SLC58A2 oligosaccharyltransferase 3 homolog A (S. cerevisiae)	Homo sapiens (human)	Peutz-Jeghers syndrome agnosia autosomal recessive intellectual developmental disorder 7 autosomal recessive intellectual developmental disorder bacterial infectious disease bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral degeneration childhood osteosarcoma chondrosarcoma choreatic disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation depressive disorder developmental coordination disorder dysthymic disorder dystonia embryoma epilepsy esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma focal epilepsy giant cell glioblastoma glioblastoma gliosarcoma hemochromatosis type 1 hemochromatosis hepatocellular carcinoma high grade glioma inflammatory bowel disease 1 inflammatory bowel disease intellectual disability large intestine cancer learning disability lingual-facial-buccal dyskinesia liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder melancholic depression microcephaly mixed glioma neurotic disorder nonpapillary renal cell carcinoma obsolete infantile epileptic encephalopathy obsolete melancholia osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma partial motor epilepsy prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia squamous cell carcinoma stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 tongue squamous cell carcinoma ulcerative colitis visual epilepsy von Hippel-Lindau disease
799443	beta 3-glucosyltransferase a	b3glcta	Danio rerio (zebrafish)	Peters plus syndrome
33844	uncharacterized protein	CG9109	Drosophila melanogaster (fruit fly)	Peters plus syndrome
108709947	beta 3-glucosyltransferase S homeolog	b3glct.S	Xenopus laevis (African clawed frog)	Peters plus syndrome
100127336	beta 3-glucosyltransferase L homeolog	b3glct.L	Xenopus laevis (African clawed frog)	Peters plus syndrome
178968	N-acetylgalactosaminide beta-1,3-galactosyltransferase	ZC250.2	Caenorhabditis elegans	Peters plus syndrome

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