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	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 **6576 - 6600** of **9988** in total

« First

‹ Prev

…

260

261

262

263

264

265

266

267

268

…

Next ›

Last »
Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
8074	fibroblast growth factor 23	FGF23	Homo sapiens (human)
8065	cullin 5	CUL5	Homo sapiens (human)
8050	pyruvate dehydrogenase complex component X	PDHX Aliases: DLDBP E3BP OPDX PDX1 proX	Homo sapiens (human)	B-cell lymphoma Leigh disease MHC class II deficiency Zollinger-Ellison syndrome adenocarcinoma adenoma adenosine deaminase deficiency brain disease breast cancer breast carcinoma cancer colorectal cancer colorectal carcinoma craniosynostosis cribriform carcinoma diabetes mellitus diabetic ketoacidosis disease of metabolism dystonia embryoma endocrine pancreas disease epilepsy familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 granular cell carcinoma hyperglycemia hyperinsulinemic hypoglycemia hyperinsulinism in situ carcinoma insulinoma intellectual disability kidney cancer lactic acidosis large intestine cancer learning disability locked-in syndrome maturity-onset diabetes of the young type 4 maturity-onset diabetes of the young microcephaly microphthalmia neonatal diabetes obsolete Matthew-Wood syndrome obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma optic atrophy ovarian carcinoma ovarian mucinous neoplasm ovarian papillary neoplasm pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatic ductal carcinoma paraplegia patent ductus arteriosus placental insufficiency polycystic kidney disease 1 primary biliary cholangitis pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency quadriplegia sarcoma severe combined immunodeficiency systemic lupus erythematosus transient neonatal diabetes mellitus tubular adenocarcinoma 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 visual epilepsy
8038	ADAM metallopeptidase domain 12	ADAM12	Homo sapiens (human)
8036	SHOC2 leucine rich repeat scaffold protein	SHOC2	Homo sapiens (human)
8034	solute carrier family 25 member 16	SLC25A16	Homo sapiens (human)
8031	nuclear receptor coactivator 4	NCOA4	Homo sapiens (human)
8030	coiled-coil domain containing 6	CCDC6	Homo sapiens (human)
8029	cubilin	CUBN	Homo sapiens (human)
8028	MLLT10 histone lysine methyltransferase DOT1L cofactor	MLLT10	Homo sapiens (human)
8021	nucleoporin 214	NUP214	Homo sapiens (human)
8019	bromodomain containing 3	BRD3	Homo sapiens (human)
8013	nuclear receptor subfamily 4 group A member 3	NR4A3	Homo sapiens (human)
8001	glycine receptor alpha 3	GLRA3	Homo sapiens (human)
8000	prostate stem cell antigen	PSCA	Homo sapiens (human)
7994	lysine acetyltransferase 6A	KAT6A	Homo sapiens (human)
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
7984	Rho guanine nucleotide exchange factor 5	ARHGEF5	Homo sapiens (human)
7982	suppression of tumorigenicity 7	ST7	Homo sapiens (human)
7980	tissue factor pathway inhibitor 2	TFPI2	Homo sapiens (human)
7976	frizzled class receptor 3	FZD3	Homo sapiens (human)
7975	MAF bZIP transcription factor K	MAFK	Homo sapiens (human)
7957	EPM2A glucan phosphatase, laforin	EPM2A Aliases: LD LDE	Homo sapiens (human)	Alzheimer's disease Balo concentric sclerosis Dravet syndrome Lafora disease MERRF syndrome Rett syndrome Unverricht-Lundborg syndrome adrenoleukodystrophy adult lymphoma agnosia alexia apraxia benign epilepsy with centrotemporal spikes blepharospasm blindness cancer central nervous system disease central nervous system lymphoma cerebral degeneration childhood lymphoma cystinuria dementia dentatorubral-pallidoluysian atrophy depressive disorder dyslexia dysthymic disorder early myoclonic encephalopathy embryoma endometrial carcinoma epilepsy focal hand dystonia galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease intellectual disability learning disability lymphoma major depressive disorder melancholic depression narcolepsy neurodegenerative disease neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis neurotic disorder non-syndromic X-linked intellectual disability obsolete Dravet syndrome obsolete infantile epileptic encephalopathy obsolete melancholia obsolete ymphosarcoma photosensitive epilepsy photosensitivity disease progressive myoclonus epilepsy 1A progressive myoclonus epilepsy 4 progressive myoclonus epilepsy psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder status epilepticus
7942	transcription factor EB	TFEB	Homo sapiens (human)
7941	phospholipase A2 group VII	PLA2G7 Aliases: LDL-PLA2 PAFAH	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 IgA glomerulonephritis Kawasaki disease Norum disease Pick's disease Reye syndrome Tangier disease X-linked dilated cardiomyopathy abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 abetalipoproteinemia acoustic neuroma acquired immunodeficiency syndrome acute chest syndrome acute myocardial infarction acute pancreatitis adult respiratory distress syndrome allergic asthma allergic rhinitis amyloidosis angiomatous meningioma aortic valve disease 1 aortic valve disease aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atrial fibrillation background diabetic retinopathy bacterial sepsis benign meningioma bicuspid aortic valve disease blind loop syndrome brain stem infarction cancer cardiomyopathy cardiovascular system disease carotid artery disease carotid artery thrombosis carotid stenosis cerebral artery occlusion cerebral convexity meningioma cerebral degeneration cerebral infarction cerebrovascular disease choreaacanthocytosis clear cell meningioma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congestive heart failure coronary artery disease coronary artery vasospasm coronary thrombosis dementia depressive disorder dermatitis diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic macular edema diabetic retinopathy dilated cardiomyopathy 1A dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy distal arthrogryposis end stage renal disease endomyocardial fibrosis essential hypertension exudative vitreoretinopathy familial adenomatous polyposis 1 familial adenomatous polyposis familial hypercholesterolemia familial hyperlipidemia familial hypertrophic cardiomyopathy familial hypobetalipoproteinemia 1 familial nephrotic syndrome fibrous meningioma generalized atherosclerosis gestational diabetes glomerulonephritis glomerulosclerosis heart disease hemolytic-uremic syndrome human immunodeficiency virus infectious disease hypertension hypertrophic cardiomyopathy hyperuricemia hypobetalipoproteinemia hypolipoproteinemia inflammatory bowel disease 1 inflammatory bowel disease inherited metabolic disorder intraorbital meningioma intraventricular meningioma intrinsic asthma islet cell tumor kidney failure large intestine cancer lipoid nephrosis meningioma meningothelial meningioma metabolic dysfunction-associated steatotic liver disease microcystic meningioma multiple sclerosis myocardial infarction nasopharynx carcinoma nephrotic syndrome type 2 nephrotic syndrome newborn respiratory distress syndrome nutmeg liver obesity obsolete eye and adnexa disease obsolete melancholia obsolete type 1 diabetes mellitus 9 obstructive sleep apnea olfactory groove meningioma pancreatitis parapsoriasis parasagittal meningioma peripheral artery disease pituitary adenoma polycystic ovary syndrome primary pulmonary hypertension proliferative diabetic retinopathy prostate cancer prostate carcinoma proteinuria psammomatous meningioma psoriasis pulmonary hypertension pustulosis of palm and sole retinal disease retinitis rheumatoid arthritis schizophrenia secretory meningioma silent myocardial infarction spinal meningioma steatotic liver disease transient cerebral ischemia transitional meningioma 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 uremia vascular disease vasomotor rhinitis vertebrobasilar insufficiency

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

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements