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 **9101 - 9125** of **9988** in total

« First

‹ Prev

…

361

362

363

364

365

366

367

368

369

…

Next ›

Last »
Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
9794	mastermind like transcriptional coactivator 1	MAML1	Homo sapiens (human)
2542	solute carrier family 37 member 4	SLC37A4 Aliases: G6PT GSD1b GSD1c GSD1d Glucose-6-phosphate exchanger SLC37A4 SPX4 glucose-6-phosphatase transporter sugar-phosphate exchange protein 4	Homo sapiens (human)	Gerstmann-Straussler-Scheinker syndrome Gorham's disease Laron syndrome achondroplasia acute pancreatitis agranulocytosis aphthous stomatitis autoimmune disease autoimmune lymphoproliferative syndrome brain cancer cancer central nervous system cancer congenital disorder of glycosylation type II cystinuria diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma essential hypertension eyelid disease familial hyperlipidemia focal segmental glomerulosclerosis galactosemia giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis 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 Ib glycogen storage disease Ic glycogen storage disease gout hepatoblastoma hepatocellular carcinoma high grade glioma hypertension hyperuricemia hypoglycemia immune system disease inherited metabolic disorder kidney disease kidney failure kwashiorkor lactic acidosis leukopenia liver cancer marasmus mixed glioma nephritis nephrolithiasis nephrosis neutropenia nutrition disease obesity obsolete type 1 diabetes mellitus 9 osteoporosis pancreatitis polycystic ovary syndrome primary pulmonary hypertension protein-energy malnutrition proteinuria pyoureter severe congenital neutropenia sudden infant death syndrome 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 uric acid nephrolithiasis xanthomatosis
4292	mutL homolog 1	MLH1	Homo sapiens (human)
200407	cellular repressor of E1A stimulated genes 2	CREG2	Homo sapiens (human)
55245	ubiquinol-cytochrome c reductase complex assembly factor 1	UQCC1	Homo sapiens (human)
5724	platelet activating factor receptor	PTAFR	Homo sapiens (human)
23248	regulation of nuclear pre-mRNA domain containing 2	RPRD2	Homo sapiens (human)
10482	nuclear RNA export factor 1	NXF1	Homo sapiens (human)
5212	vitrin	VIT	Homo sapiens (human)
340547	V-set and immunoglobulin domain containing 1	VSIG1	Homo sapiens (human)
170692	ADAM metallopeptidase with thrombospondin type 1 motif 18	ADAMTS18	Homo sapiens (human)
30814	phospholipase A2 group IIE	PLA2G2E	Homo sapiens (human)	atopic dermatitis benign mastocytoma dermatitis extracutaneous mastocytoma indolent systemic mastocytosis mast cell neoplasm mastocytosis obesity
140467	zinc finger protein 358	ZNF358	Homo sapiens (human)
83642	selenoprotein O	SELENOO	Homo sapiens (human)
3155	3-hydroxy-3-methylglutaryl-CoA lyase	HMGCL Aliases: HL hydroxymethylglutaricaciduria hydroxymethylglutaryl-CoA lyase	Homo sapiens (human)	Unverricht-Lundborg syndrome X-linked dilated cardiomyopathy acute pancreatitis amino acid metabolic disorder anemia blepharospasm brain disease cancer cardiac arrest congestive heart failure diarrhea 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 early myoclonic encephalopathy epilepsy focal hand dystonia hyperlysinemia hyperuricemia hypoglycemia hypoglycemic coma intellectual disability lactic acidosis learning disability leukopenia macrocytic anemia melanoma microcephaly mitochondrial metabolism disease mitochondrial myopathy obsolete infantile epileptic encephalopathy pancreatitis skin melanoma syndromic X-linked intellectual disability 94 thrombocytosis urea cycle disorder visual epilepsy
1639	dynactin subunit 1	DCTN1	Homo sapiens (human)
4598	mevalonate kinase	MVK	Homo sapiens (human)
5315	pyruvate kinase M1/2	PKM Aliases: OIP3 PK3 THBP1	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 B-cell lymphoma Bloom syndrome Clostridium difficile colitis Cockayne syndrome Crohn's colitis Crohn's disease Gilles de la Tourette syndrome Klatskin's tumor Li-Fraumeni syndrome 1 Li-Fraumeni syndrome Pick's disease Reye syndrome Van der Woude syndrome abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adult medulloblastoma amnestic disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bacterial sepsis bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bone osteosarcoma brain cancer brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood leukemia childhood medulloblastoma childhood osteosarcoma childhood type dermatomyositis cholangiocarcinoma choriocarcinoma chromophobe renal cell carcinoma chronic cholangitis chronic fatigue syndrome chronic myeloid leukemia clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis cribriform carcinoma cutaneous fibrous histiocytoma cystic fibrosis dermatomyositis disease of metabolism distal arthrogryposis embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma endometrial hyperplasia enterocele esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension gallbladder cancer gallbladder carcinoma gallbladder disease gastroenteritis gastrointestinal stromal tumor giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glucose intolerance goiter granular cell carcinoma granulosa cell tumor head and neck cancer head and neck squamous cell carcinoma hepatitis C hepatocellular carcinoma hidradenoma high grade glioma hyperglycemia hyperhomocysteinemia hypertension ileitis ileocolitis immune system disease in situ carcinoma inflammatory bowel disease 1 inflammatory bowel disease influenza intrahepatic cholangiocarcinoma irritable bowel syndrome kidney cancer large intestine cancer leukemia liver cancer liver carcinoma liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma microphthalmia mixed glioma multiple myeloma mycosis fungoides myelitis myeloproliferative disorder with eosinophilia myocardial infarction myositis nasopharynx carcinoma nephritis neurocirculatory asthenia nonpapillary renal cell carcinoma nontoxic goiter obesity obsolete Matthew-Wood syndrome obsolete hilar cholangiocellular carcinoma obsolete ymphosarcoma osteoarthritis osteoporosis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenocarcinoma papillary renal cell carcinoma papillary transitional carcinoma placenta cancer prediabetes syndrome primary cutaneous T-cell non-Hodgkin lymphoma primary cutaneous amyloidosis primary pulmonary hypertension prostate cancer prostate carcinoma psoriatic arthritis reflex sympathetic dystrophy renal carcinoma renal cell carcinoma renal infectious disease retrograde amnesia sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin benign neoplasm skin cancer skin melanoma skin papilloma skin tag squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma syringoma systemic Epstein-Barr virus positive T-cell lymphoma of childhood thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland disease thyroid gland papillary carcinoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis urinary bladder cancer uterine corpus cancer viral infectious disease
71	actin gamma 1	ACTG1	Homo sapiens (human)
8527	diacylglycerol kinase delta	DGKD Aliases: DGKdelta KIAA0145 diglyceride kinase	Homo sapiens (human)	Lennox-Gastaut syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease cancer diabetes mellitus embryoma epilepsy hyperglycemia nephrolithiasis obsessive-compulsive disorder open-angle glaucoma primary open angle glaucoma type 2 diabetes mellitus uric acid nephrolithiasis visual epilepsy
128367	olfactory receptor family 10 subfamily X member 1	OR10X1	Homo sapiens (human)
51649	mitochondrial ribosomal protein S23	MRPS23	Homo sapiens (human)
2645	glucokinase	GCK Aliases: HK4 hexokinase 4	Homo sapiens (human)	Chagas disease Fanconi anemia complementation group C Fanconi anemia Laron syndrome Marfan syndrome Werner syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acute chest syndrome adult-onset Still's disease agnosia apraxia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome bronchus cancer bronchus carcinoma cancer cardiovascular system disease chronic fatigue syndrome congenital heart disease congenital ptosis coronary artery disease diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy disease of metabolism embryoma encephalitis encephalomyelitis endocrine pancreas disease epilepsy essential hypertension familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 familial hyperinsulinemic hypoglycemia 3 generalized anxiety disorder gestational diabetes glomerulonephritis glucose intolerance glucose metabolism disease heart disease hepatocellular carcinoma hyperglycemia hyperinsulinemic hypoglycemia hyperinsulinism hypertension hypoglycemia hypoglycemic coma immune system disease insulinoma intellectual disability kidney disease learning disability leishmaniasis liver cancer liver carcinoma liver cirrhosis lung benign neoplasm lung cancer lung carcinoma maturity-onset diabetes of the young type 2 maturity-onset diabetes of the young type 3 maturity-onset diabetes of the young myelitis myotonic dystrophy type 1 myotonic dystrophy type 2 neonatal diabetes nephritis nephrosis neuropathy nutmeg liver obesity obsolete infantile epileptic encephalopathy obsolete type 1 diabetes mellitus 9 osteoarthritis pancreatic cancer pancreatic carcinoma peripheral nervous system disease permanent neonatal diabetes mellitus placental insufficiency polyneuropathy prediabetes syndrome progeria prostate cancer prostate carcinoma ptosis pyoureter retinal disease retinitis rheumatoid arthritis sensorineural hearing loss situs inversus steatotic liver disease syndromic X-linked intellectual disability 94 systemic lupus erythematosus transient neonatal diabetes mellitus trypanosomiasis 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 urea cycle disorder visceral leishmaniasis visual epilepsy
284004	hexosaminidase D	HEXD Aliases: FLJ23825 hexosaminidase D, cytosolic	Homo sapiens (human)	GM2 gangliosidosis Gilles de la Tourette syndrome Marfan syndrome Sandhoff disease Tay-Sachs disease Timothy syndrome dystonia lingual-facial-buccal dyskinesia long QT syndrome 8 situs inversus tricuspid valve stenosis tuberous sclerosis 1 tuberous sclerosis
10057	ATP binding cassette subfamily C member 5	ABCC5	Homo sapiens (human)

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