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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	October 29, 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 **8601 - 8625** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
134957	syntaxin binding protein 5	STXBP5	Homo sapiens (human)
29091	syntaxin binding protein 6	STXBP6	Homo sapiens (human)
10923	SUB1 regulator of transcription	SUB1	Homo sapiens (human)
8803	succinate-CoA ligase ADP-forming subunit beta	SUCLA2 Aliases: succinate--CoA ligase (ADP-forming)	Homo sapiens (human)	3-methylglutaconic aciduria type 4 Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 3 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Creutzfeldt-Jakob disease Crohn's colitis Crohn's disease Down syndrome Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Laron syndrome Leigh disease Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome achondroplasia age related macular degeneration alternating hemiplegia of childhood amnestic disorder amyloidosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autonomic neuropathy blindness central nervous system disease cerebral degeneration congenital ptosis congestive heart failure coronary artery disease cutaneous porphyria degeneration of macula and posterior pole dementia depressive disorder diabetes mellitus diabetic ketoacidosis dissociative amnesia dysthymic disorder dystonia enterocele epilepsy erythropoietic protoporphyria familial retinoblastoma focal hand dystonia frontotemporal dementia generalized dystonia herpes simplex hydrocephalus hypertropia inflammatory bowel disease 1 inflammatory bowel disease isolated elevated serum creatine phosphokinase levels lactic acidosis leukopenia lingual-facial-buccal dyskinesia macular degeneration major depressive disorder mechanical strabismus melancholic depression methylmalonic acidemia microcephaly mitochondrial DNA depletion syndrome 5 mitochondrial DNA depletion syndrome 9 mitochondrial DNA depletion syndrome mitochondrial encephalomyopathy movement disease nervous system disease neuroblastoma neurodegenerative disease neuropathy neurotic disorder obesity obsolete melancholia ophthalmoplegia parasitic helminthiasis infectious disease peripheral nervous system disease ptosis retinoblastoma retrocochlear disease retrograde amnesia sensorineural hearing loss sideroblastic anemia 1 strabismus trichohepatoenteric syndrome 1 trichohepatoenteric syndrome trilateral retinoblastoma tuberculosis type 2 diabetes mellitus ulcerative colitis vascular dementia visual epilepsy
8802	succinate-CoA ligase GDP/ADP-forming subunit alpha	SUCLG1	Homo sapiens (human)	Leigh disease McCune Albright syndrome brain disease cardiomyopathy central nervous system cancer cerebral degeneration endomyocardial fibrosis epilepsy familial hypertrophic cardiomyopathy giant cell glioblastoma glioblastoma gliosarcoma high grade glioma hypertrophic cardiomyopathy hypoglycemia hypophosphatemia intellectual disability lactic acidosis learning disability methylmalonic acidemia mitochondrial DNA depletion syndrome 5 mitochondrial DNA depletion syndrome 9 mitochondrial DNA depletion syndrome mitochondrial encephalomyopathy mixed glioma skin disease stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 visual epilepsy
8801	succinate-CoA ligase GDP-forming subunit beta	SUCLG2	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Pick's disease Reye syndrome cerebral degeneration endometriosis of ovary endometriosis methylmalonic acidemia prostate cancer prostate carcinoma
56670	succinate receptor 1	SUCNR1	Homo sapiens (human)
51430	SUN domain containing ossification factor	SUCO	Homo sapiens (human)
64426	SDS3 homolog, SIN3A corepressor complex component	SUDS3	Homo sapiens (human)
57794	SURP and G-patch domain containing 1	SUGP1	Homo sapiens (human)
10147	SURP and G-patch domain containing 2	SUGP2	Homo sapiens (human)
10910	SGT1 homolog, MIS12 kinetochore complex assembly cochaperone	SUGT1	Homo sapiens (human)
23213	sulfatase 1	SULF1 Aliases: Extracellular sulfatase Sulf-1 KIAA1077 SULF-1 hSulf-1	Homo sapiens (human)	Marinesco-Sjogren syndrome acute pancreatitis adult hepatocellular carcinoma anal carcinoma in situ arthritis arthropathy bacterial sepsis bladder urothelial carcinoma brain cancer breast cancer breast carcinoma breast ductal carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cervix uteri carcinoma in situ childhood hepatocellular carcinoma colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma degenerative disc disease disease of metabolism embryoma giant cell glioblastoma glioblastoma head and neck squamous cell carcinoma hepatitis hepatocellular carcinoma high grade glioma idiopathic interstitial pneumonia large intestine cancer liver cancer liver carcinoma liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma melanoma nodular prostate osteoarthritis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatitis pneumonia postinflammatory pulmonary fibrosis primary cerebellar degeneration prostatic adenoma pulmonary fibrosis seminoma skin melanoma steatotic liver disease stomach cancer stomach carcinoma testicular cancer testis seminoma transitional cell carcinoma
55959	sulfatase 2	SULF2 Aliases: HSULF-2 KIAA1247 SULF-2	Homo sapiens (human)	acute pancreatitis adenocarcinoma adenoma arthritis arthropathy brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma cribriform carcinoma diabetes mellitus dilated cardiomyopathy 1A dilated cardiomyopathy embryoma endometriosis of ovary endometriosis of uterus endometriosis essential hypertension giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hepatocellular carcinoma high grade glioma hyperlipoproteinemia type III hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis invasive ductal carcinoma large intestine cancer liver cancer liver carcinoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma mixed glioma neuroblastoma nonpapillary renal cell carcinoma obesity osteoarthritis pancreatic cancer pancreatic carcinoma pancreatitis papillary renal cell carcinoma parapsoriasis postinflammatory pulmonary fibrosis prostate cancer prostate carcinoma psoriasis pulmonary fibrosis pure red-cell aplasia pustulosis of palm and sole renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma seminoma skin benign neoplasm skin cancer squamous cell carcinoma stomach cancer stomach carcinoma testicular cancer testis seminoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus uveal melanoma
27284	sulfotransferase family 1B member 1	SULT1B1	Homo sapiens (human)
6819	sulfotransferase family 1C member 2	SULT1C2	Homo sapiens (human)
6783	sulfotransferase family 1E member 1	SULT1E1 Aliases: EST	Homo sapiens (human)	Alzheimer's disease Axenfeld-Rieger syndrome type 2 Creutzfeldt-Jakob disease DiGeorge syndrome Down syndrome Laron syndrome Marfan syndrome Richter's syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acute myocardial infarction acute myocarditis adult lymphoma adult medulloblastoma adult oligodendroglioma alcoholic hepatitis amyotrophic lateral sclerosis androgen insensitivity syndrome ankylosing spondylitis aortic disease arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation autosomal recessive limb-girdle muscular dystrophy type 2C bacterial sepsis bone osteosarcoma brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cannabis abuse cannabis dependence carcinoma cardiomyopathy cardiovascular system disease central nervous system lymphoma cerebral infarction cerebrovascular disease childhood T-cell acute lymphoblastic leukemia childhood lymphoma childhood medulloblastoma childhood oligodendroglioma childhood osteosarcoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chronic fatigue syndrome chronic lymphocytic leukemia colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary aneurysm coronary artery disease coronary stenosis coronary thrombosis craniosynostosis cystic fibrosis depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dysentery dysthymic disorder embryoma encephalomyelitis endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of uterus endometriosis endomyocardial fibrosis essential hypertension eye disease familial hypertrophic cardiomyopathy gallbladder disease gastric adenocarcinoma glomerulonephritis head and neck cancer head and neck squamous cell carcinoma heart disease hemochromatosis type 1 hemochromatosis hepatocellular carcinoma hereditary multiple exostoses hidradenitis suppurativa hidradenitis high grade glioma hyperglycemia hypertension hypertrophic cardiomyopathy inferior myocardial infarction inflammatory bowel disease 1 inflammatory bowel disease intellectual disability intermediate coronary syndrome kidney disease large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer learning disability liver cancer liver disease lung benign neoplasm lung cancer lung carcinoma lymphoma major depressive disorder medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma mitochondrial metabolism disease mitral valve stenosis mixed oligodendroglioma-astrocytoma multiple endocrine neoplasia type 1 myocardial infarction nephritis nephrosis neurotic disorder nodular prostate obesity obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oligodendroglioma osteosarcoma ovarian cancer ovarian carcinoma peripheral artery disease polycystic ovary syndrome pompholyx primary hyperoxaluria primary open angle glaucoma primary pulmonary hypertension progressive muscular atrophy proliferative type fibrocystic change of breast prostate cancer prostate carcinoma prostatic adenoma pyoureter retinal disease retinitis schizophrenia 1 schizophrenia scleroderma severe acute respiratory syndrome silent myocardial infarction situs inversus steatotic liver disease stomach cancer stomach carcinoma systemic scleroderma tetralogy of Fallot thymic carcinoma thymoma transient cerebral ischemia tuberous sclerosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis uterine corpus cancer velocardiofacial syndrome vertebrobasilar insufficiency
6822	sulfotransferase family 2A member 1	SULT2A1	Homo sapiens (human)
6820	sulfotransferase family 2B member 1	SULT2B1 Aliases: HSST2	Homo sapiens (human)	Laron syndrome Sjogren-Larsson syndrome achondroplasia acquired hyperkeratosis autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 14 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis bacterial sepsis cholestasis ectropion endometrial cancer endometrial carcinoma gallbladder cancer gallbladder carcinoma granuloma annulare hepatocellular carcinoma hypotrichosis ichthyosis keratosis follicularis kidney failure liver cancer mongolian spot obsolete congenital ichthyosiform erythroderma otitis media prostate cancer prostate carcinoma pseudoxanthoma elasticum uterine corpus cancer
285362	sulfatase modifying factor 1	SUMF1 Aliases: FGE UNQ3037	Homo sapiens (human)	Balo concentric sclerosis Laron syndrome X-linked chondrodysplasia punctata 1 X-linked ichthyosis achondroplasia adrenoleukodystrophy autosomal dominant cerebellar ataxia autosomal dominant chondrodysplasia punctata autosomal recessive spinocerebellar ataxia 16 blindness breast cancer breast carcinoma cancer cataract central nervous system disease cerebral degeneration chondrodysplasia punctata chronic obstructive pulmonary disease communicating hydrocephalus cystic fibrosis embryoma epilepsy hydrocephalus ichthyosis inherited metabolic disorder intellectual disability learning disability lysosomal storage disease metachromatic leukodystrophy microcephaly mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis mucosulfatidosis multiple sclerosis narcolepsy obstructive hydrocephalus optic atrophy recurrent corneal erosion retinal degeneration rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 schizophrenia senile degeneration of brain sensorineural hearing loss visual epilepsy
25870	sulfatase modifying factor 2	SUMF2	Homo sapiens (human)
7341	small ubiquitin like modifier 1	SUMO1	Homo sapiens (human)
23353	Sad1 and UNC84 domain containing 1	SUN1	Homo sapiens (human)
25777	Sad1 and UNC84 domain containing 2	SUN2	Homo sapiens (human)
11198	SPT16 homolog, facilitates chromatin remodeling subunit	SUPT16H	Homo sapiens (human)

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