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	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 **801 - 825** of **1582** in total

« First

‹ Prev

…

29

30

31

32

33

34

35

36

37

…

Next ›

Last »
Gene ID	Gene Name ▲	Gene Symbol	Organism	Disease Ontology
2882	glutathione peroxidase 7	GPX7 Aliases: FLJ14777 GPX6 NPGPx	Homo sapiens (human)	Barrett's adenocarcinoma Barrett's esophagus Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease amyotrophic lateral sclerosis breast cancer breast carcinoma bronchiolo-alveolar adenocarcinoma cancer embryoma esophagus adenocarcinoma hyperhomocysteinemia lung cancer progressive muscular atrophy
493869	glutathione peroxidase 8 (putative)	GPX8 Aliases: EPLA847 UNQ847	Homo sapiens (human)
2597	glyceraldehyde-3-phosphate dehydrogenase	GAPDH	Homo sapiens (human)	ACTH-secreting pituitary adenoma 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 Burkitt lymphoma Cockayne syndrome Cornelia de Lange syndrome Crohn's colitis Crohn's disease Down syndrome Dubowitz syndrome Ewing sarcoma HELLP syndrome Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease IgA glomerulonephritis Japanese encephalitis Kawasaki disease Kennedy's disease Keshan disease Laron syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Prader-Willi syndrome Reye syndrome Robinow syndrome Seckel syndrome Sertoli cell-only syndrome Silver-Russell syndrome Turner syndrome X-linked Aarskog syndrome X-linked spermatogenic failure 1 Zika fever achondroplasia acidophil adenoma acoustic neuroma acute lymphoblastic leukemia acute megakaryocytic leukemia acute poststreptococcal glomerulonephritis adenosarcoma adrenal adenoma adrenal cortex cancer alcohol dependence alcohol use disorder alcoholic cardiomyopathy alcoholic hepatitis allergic asthma amyloidosis amyotrophic lateral sclerosis angioimmunoblastic T-cell lymphoma angiomatous meningioma aortic aneurysm aortic valve disease 1 aortic valve disease 2 aortic valve stenosis arthritis arthropathy asthma autoimmune disease autoimmune lymphoproliferative syndrome autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome bacterial sepsis basal cell carcinoma benign meningioma bicuspid aortic valve disease bladder carcinoma bone osteosarcoma brain glioma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy central nervous system cancer cerebral convexity meningioma cerebral degeneration cervical cancer cervix carcinoma childhood osteosarcoma chondrodysplasia-pseudohermaphroditism syndrome chromophobe renal cell carcinoma chronic fatigue syndrome clear cell meningioma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease dengue disease dentatorubral-pallidoluysian atrophy developmental and epileptic encephalopathy 2 diabetes mellitus diabetic cataract diabetic retinopathy diffuse large B-cell lymphoma dysplastic nevus syndrome early infantile epileptic encephalopathy embryoma encephalitis encephalomyelitis endocrine exophthalmos endomyocardial fibrosis epilepsy esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma familial hypertrophic cardiomyopathy fasciitis fibrous meningioma follicular lymphoma ganglioneuroblastoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis gonadal dysgenesis granuloma annulare hepatitis B hepatitis C hepatitis D hepatocellular carcinoma hereditary spherocytosis high grade glioma hypertrophic cardiomyopathy hypopharynx cancer immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza intestinal schistosomiasis intraorbital meningioma intraventricular meningioma intrinsic asthma kidney disease large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer late onset Parkinson's disease leishmaniasis liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphangioleiomyomatosis malaria melanoma membranous glomerulonephritis meningioma meningothelial meningioma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic meningioma microphthalmia middle cerebral artery infarction mixed glioma multiple endocrine neoplasia type 1 multiple myeloma multiple sclerosis myelitis nephritis nephroblastoma neuroblastoma neurodegenerative disease neuroectodermal tumor nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood syndrome obsolete infantile epileptic encephalopathy obsolete ymphosarcoma olfactory groove meningioma oral squamous cell carcinoma osteoarthritis osteoporosis osteosarcoma ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma parapsoriasis parasagittal meningioma pituitary adenoma placental insufficiency pre-eclampsia progressive muscular atrophy progressive myoclonus epilepsy prolactinoma prostate cancer prostate carcinoma psammomatous meningioma psoriasis pustulosis of palm and sole reflex sympathetic dystrophy renal carcinoma renal cell carcinoma rheumatic heart disease sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia secretory meningioma sickle cell anemia skin melanoma sleeping sickness spinal meningioma spinal muscular atrophy status epilepticus stomach cancer stomach carcinoma tarsal-carpal coalition syndrome thymic carcinoma thymoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma transitional meningioma trypanosomiasis tuberculosis type 2 diabetes mellitus ulcerative colitis urinary bladder cancer viral infectious disease visceral leishmaniasis yellow fever
26330	glyceraldehyde-3-phosphate dehydrogenase, spermatogenic	GAPDHS Aliases: GAPD2 GAPDH-2	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 Creutzfeldt-Jakob disease Pick's disease Reye syndrome cancer cerebral degeneration diabetes mellitus diabetic ketoacidosis embryoma melanoma skin melanoma
132158	glycerate kinase	GLYCTK Aliases: HBEBP2 HBEBP4	Homo sapiens (human)	D-glyceric aciduria Unverricht-Lundborg syndrome blepharospasm brain disease early myoclonic encephalopathy epilepsy focal hand dystonia glycine encephalopathy intellectual disability lactic acidosis learning disability locked-in syndrome microcephaly obsolete infantile epileptic encephalopathy primary hyperoxaluria quadriplegia schizophrenia visual epilepsy
2710	glycerol kinase	GK Aliases: GK1 GKD	Homo sapiens (human)	Aland Island eye disease Becker muscular dystrophy Duchenne muscular dystrophy Kallmann syndrome Klinefelter syndrome Laron syndrome Patau syndrome Sheehan syndrome X-linked adrenal hypoplasia congenita achondroplasia autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy chromosome Xp21 deletion syndrome cone-rod dystrophy congenital muscular dystrophy coronary artery disease diabetes mellitus distal myopathy endomyocardial fibrosis facioscapulohumeral muscular dystrophy familial hypercholesterolemia fundus albipunctatus galactokinase deficiency galactosemia glycerol kinase deficiency hypertropia hypoglycemia hypogonadism hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism intellectual disability isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency learning disability limb-girdle muscular dystrophy mechanical strabismus muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 obesity obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy ophthalmoplegia osteoporosis panhypopituitarism placental insufficiency retinitis pigmentosa rippling muscle disease 2 strabismus tuberculosis type 2 diabetes mellitus
2712	glycerol kinase 2	GK2 Aliases: GKTA	Homo sapiens (human)	glycerol kinase deficiency
256356	glycerol kinase 5	GK5	Homo sapiens (human)
150763	glycerol-3-phosphate acyltransferase 2, mitochondrial	GPAT2 Aliases: CT123 cancer/testis antigen 123	Homo sapiens (human)	adrenoleukodystrophy breast cancer breast carcinoma cancer melanoma skin melanoma
84803	glycerol-3-phosphate acyltransferase 3	GPAT3 Aliases: AGPAT10 HMFN0839 LPAAT-theta MAG1 MGC11324 lysophosphatidic acid acyltransferase, theta	Homo sapiens (human)	acquired immunodeficiency syndrome acute myeloid leukemia breast cancer cancer endometritis human immunodeficiency virus infectious disease leech infestation myiasis obesity toxoplasmosis
137964	glycerol-3-phosphate acyltransferase 4	GPAT4 Aliases: DKFZp586M1819 LPAAT-zeta TSARG7 lysophosphatidic acid acyltransferase, zeta	Homo sapiens (human)	diabetes mellitus type 2 diabetes mellitus
57678	glycerol-3-phosphate acyltransferase, mitochondrial	GPAM Aliases: GPAT1 KIAA1560 MGC26846 glycerol-3-phosphate acyltransferase 1, mitochondrial	Homo sapiens (human)	cancer embryoma familial nephrotic syndrome lipoid nephrosis melanoma metabolic dysfunction-associated steatotic liver disease nephrotic syndrome obesity overnutrition skin melanoma steatotic liver disease
2819	glycerol-3-phosphate dehydrogenase 1	GPD1	Homo sapiens (human)	Laron syndrome Refsum disease Zellweger syndrome achondroplasia breast cancer breast carcinoma cancer central nervous system cancer diabetes mellitus embryoma giant cell glioblastoma glioblastoma gliosarcoma hepatocellular carcinoma high grade glioma infantile Refsum disease inherited metabolic disorder liver cancer liver cirrhosis maturity-onset diabetes of the young mixed glioma obesity obstructive sleep apnea peroxisome biogenesis disorder 1A steatotic liver disease type 2 diabetes mellitus
23171	glycerol-3-phosphate dehydrogenase 1 like	GPD1L Aliases: KIAA0089	Homo sapiens (human)	Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrial fibrillation congestive heart failure coronary artery disease head and neck squamous cell carcinoma nutmeg liver osteoarthritis sick sinus syndrome steatotic liver disease sudden infant death syndrome
2820	glycerol-3-phosphate dehydrogenase 2	GPD2	Homo sapiens (human)	cancer central nervous system cancer citrullinemia communication disorder diabetes mellitus embryoma esophagus squamous cell carcinoma gliosarcoma high grade glioma insulinoma intellectual disability intrahepatic cholestasis language disorder learning disability mixed glioma motion sickness myopia osteoporosis reflex sympathetic dystrophy thyroid adenoma thyroid cancer thyroid gland carcinoma type 2 diabetes mellitus
8443	glyceronephosphate O-acyltransferase	GNPAT Aliases: DAP-AT DAPAT DHAPAT dihydroxyacetone phosphate acyltransferase glycerone-phosphate O-acyltransferase	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 Wilson disease X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 Zellweger syndrome attention deficit hyperactivity disorder autistic disorder autosomal dominant chondrodysplasia punctata cancer cataract cerebral degeneration chondrodysplasia punctata disease of mental health embryoma hemochromatosis type 1 hemochromatosis hepatocellular carcinoma intellectual disability iron metabolism disease learning disability liver cancer liver carcinoma liver cirrhosis microcephaly peroxisome biogenesis disorder 1A rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 rhizomelic chondrodysplasia punctata schizophrenia scoliosis
56261	glycerophosphocholine phosphodiesterase 1	GPCPD1 Aliases: GDE5 GDPD6 KIAA1434	Homo sapiens (human)	eating disorder endometrial cancer endometrial carcinoma obesity uterine corpus cancer
284161	glycerophosphodiester phosphodiesterase domain containing 1	GDPD1 Aliases: FLJ37451 GDE4	Homo sapiens (human)
79153	glycerophosphodiester phosphodiesterase domain containing 3	GDPD3 Aliases: MGC4171	Homo sapiens (human)	Fabry disease Wolman disease chylomicron retention disease lipid storage disease
81544	glycerophosphodiester phosphodiesterase domain containing 5	GDPD5 Aliases: GDE2 PP1665	Homo sapiens (human)	acute myeloid leukemia breast cancer breast carcinoma cancer colorectal cancer colorectal carcinoma embryoma large intestine cancer neuroblastoma neurodegenerative disease rheumatoid arthritis
27232	glycine N-methyltransferase	GNMT	Homo sapiens (human)	glycine N-methyltransferase deficiency hepatocellular carcinoma
2653	glycine cleavage system protein H	GCSH Aliases: lipoic acid-containing protein	Homo sapiens (human)	Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Unverricht-Lundborg syndrome X-linked Aarskog syndrome amino acid metabolic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome blepharospasm brain disease breast cancer breast carcinoma cancer central nervous system lymphoma chondrodysplasia-pseudohermaphroditism syndrome early myoclonic encephalopathy embryoma epilepsy focal hand dystonia glycine encephalopathy intellectual disability learning disability lymphoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II multiple mitochondrial dysfunctions syndrome obsolete ymphosarcoma schizophrenia urea cycle disorder visual epilepsy
2731	glycine decarboxylase	GLDC Aliases: GCSP NKH glycine cleavage system protein P glycine dehydrogenase nonketotic hyperglycinemia	Homo sapiens (human)	B-cell lymphoma Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Marfan syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Unverricht-Lundborg syndrome X-linked Aarskog syndrome allergic asthma asthma autistic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome basal ganglia disease blepharospasm bone osteosarcoma brain disease bronchus cancer bronchus carcinoma cancer central nervous system cancer chondrodysplasia-pseudohermaphroditism syndrome chromosome 9p deletion syndrome communicating hydrocephalus conduct disorder disease of metabolism early myoclonic encephalopathy embryoma epilepsy focal hand dystonia frontotemporal dementia gliosarcoma glycine encephalopathy hepatocellular carcinoma high grade glioma hydrocephalus hyperglycemia idiopathic generalized epilepsy influenza intellectual disability intrinsic asthma large cell carcinoma learning disability liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II mixed glioma neuroblastoma obesity obsolete ymphosarcoma obstructive hydrocephalus osteosarcoma progressive supranuclear palsy prostate cancer prostate carcinoma red-green color blindness schizophrenia senile degeneration of brain situs inversus stomach cancer stomach carcinoma tuberous sclerosis viral infectious disease visual epilepsy
5834	glycogen phosphorylase B	PYGB Aliases: glycogen phosphorylase, brain form	Homo sapiens (human)	acute myocardial infarction adenoid cystic carcinoma breast cancer cancer coronary artery disease coronary thrombosis diabetes mellitus embryoma lung cancer lung non-small cell carcinoma myocardial infarction salivary gland adenoid cystic carcinoma salivary gland cancer silent myocardial infarction type 2 diabetes mellitus
5836	glycogen phosphorylase L	PYGL Aliases: GSD6 Hers disease glycogen phosphorylase, liver form glycogen storage disease type VI	Homo sapiens (human)	Gerstmann-Straussler-Scheinker syndrome Gorham's disease Laron syndrome achondroplasia cystinuria galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease III glycogen storage disease IV glycogen storage disease Ia glycogen storage disease V glycogen storage disease VI glycogen storage disease VII glycogen storage disease hepatocellular carcinoma hypoglycemia lactic acidosis liver cancer

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

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements