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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 **417976 - 418000** of **422592** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
10767	HBS1 like translational GTPase	HBS1L Aliases: DKFZp434g247 EF-1a ERFS HBS1 HSPC276 KIAA1038 eRF3 family member eRF3c	Homo sapiens (human)
10766	transducer of ERBB2, 2	TOB2	Homo sapiens (human)
10765	lysine demethylase 5B	KDM5B	Homo sapiens (human)
10763	nestin	NES	Homo sapiens (human)
10762	nucleoporin 50	NUP50	Homo sapiens (human)
10758	TRAF3 interacting protein 2	TRAF3IP2	Homo sapiens (human)
10752	cell adhesion molecule L1 like	CHL1	Homo sapiens (human)
10749	kinesin family member 1C	KIF1C	Homo sapiens (human)
10747	MBL associated serine protease 2	MASP2 Aliases: MAP-2 Map19 mannose-binding lectin associated protein 19 mannose-binding lectin-associated serine protease 2 sMAP	Homo sapiens (human)	B-cell lymphoma Burkitt lymphoma Chagas disease Crohn's colitis Crohn's disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Kuhnt-Junius degeneration Langerhans-cell histiocytosis Stevens-Johnson syndrome Streptococcus pneumonia angioedema autoimmune disease autoimmune lymphoproliferative syndrome bacterial sepsis cancer cardiac arrest cardiomyopathy cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ chronic fatigue syndrome colorectal cancer colorectal carcinoma complement component 2 deficiency complement component 4a deficiency complement component 4b deficiency complement component 6 deficiency complement component 7 deficiency complement component 9 deficiency complement deficiency cystic fibrosis diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma embryoma encephalomyelitis endomyocardial fibrosis erythema multiforme esophagus squamous cell carcinoma follicular lymphoma frontotemporal dementia glomerulonephritis hepatitis C hepatocellular carcinoma hereditary angioedema hypersensitivity reaction type III disease hypertrophic cardiomyopathy immune system disease inflammatory bowel disease 1 inflammatory bowel disease kidney disease large intestine cancer lepromatous leprosy leprosy liver cancer lymphoma malaria multiple sclerosis nephritis nephrosis non-Hodgkin lymphoma obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma ovarian cancer ovarian carcinoma parapsoriasis pneumonia psoriasis pustulosis of palm and sole pyoureter reticulosarcoma rheumatic fever rheumatoid arthritis sarcoidosis severe acute respiratory syndrome sporotrichosis systemic lupus erythematosus trypanosomiasis tuberculosis 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 type I complement component 8 deficiency type II complement component 8 deficiency ulcerative colitis urinary schistosomiasis viral infectious disease
10745	putative homeodomain transcription factor 1	PHTF1	Homo sapiens (human)
10743	retinoic acid induced 1	RAI1	Homo sapiens (human)
10734	STAG3 cohesin complex component	STAG3	Homo sapiens (human)
10730	YME1 like 1 ATPase	YME1L1	Homo sapiens (human)
10728	prostaglandin E synthase 3	PTGES3 Aliases: TEBP cPGES p23	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 Lyme disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome acute monocytic leukemia acute myeloid leukemia adenocarcinoma adenoma adult fibrosarcoma alexia aortic valve insufficiency atherosclerosis autism spectrum disorder autistic disorder bone osteosarcoma breast cancer breast carcinoma cancer carcinoma cerebral degeneration childhood acute lymphocytic leukemia childhood osteosarcoma cribriform carcinoma cryptosporidiosis cystic fibrosis diarrhea dyslexia embryoma esophageal cancer esophageal carcinoma familial retinoblastoma fibrosarcoma granular cell carcinoma hepatitis C intrahepatic cholestasis of pregnancy lung adenocarcinoma lung cancer lung non-small cell carcinoma neurodegenerative disease oligodendroglioma osteosarcoma papillary adenocarcinoma papillary renal cell carcinoma periodontitis prostate cancer prostate carcinoma retinoblastoma sarcomatoid carcinoma schizophrenia thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma toxic encephalopathy trilateral retinoblastoma tubular adenocarcinoma
10725	nuclear factor of activated T cells 5	NFAT5	Homo sapiens (human)
10724	O-GlcNAcase	OGA Aliases: MEA5 NCOAT nuclear cytoplasmic O-GlcNAcase and acetyltransferase	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 Fabry disease GM1 gangliosidosis GM2 gangliosidosis, AB variant GM2 gangliosidosis Gaucher's disease Gilles de la Tourette syndrome Lewy body dementia Marfan syndrome Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Sandhoff disease Tay-Sachs disease Timothy syndrome abdominal obesity-metabolic syndrome 1 acoustic neuroma acute myocardial infarction alternating hemiplegia of childhood amnestic disorder amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis angiomatous meningioma anterior horn cell disease aortic valve disease 2 aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis autonomic neuropathy autosomal dominant cerebellar ataxia autosomal recessive distal hereditary motor neuronopathy 1 benign meningioma beta thalassemia breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease central nervous system disease cerebral convexity meningioma cerebral degeneration chronic kidney disease chylomicron retention disease clear cell meningioma colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ia congenital disorder of glycosylation type I congestive heart failure connective tissue benign neoplasm coronary artery disease coronary thrombosis cystitis dermatitis diabetes mellitus diabetic ketoacidosis dystonia embryoma encephalitis encephalomyelitis epilepsy epithelioid sarcoma essential hypertension fibrous meningioma gangliosidosis gastroenteritis gastrointestinal system disease gestational diabetes giant cell glioblastoma gingivitis glioblastoma glomerulonephritis glucose intolerance glycoproteinosis heart disease hepatocellular carcinoma hydronephrosis hypertension ileitis ileocolitis intestinal disease intraorbital meningioma intraventricular meningioma kidney disease kidney failure kwashiorkor large intestine cancer lateral sclerosis lingual-facial-buccal dyskinesia lipid storage disease lipoid nephrosis liver cancer liver cirrhosis long QT syndrome 8 lung cancer lung carcinoma lymphoplasmacyte-rich meningioma lysosomal storage disease marasmus membranous glomerulonephritis meningioma meningothelial meningioma microcystic meningioma microphthalmia motor neuron disease mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IVB mucopolysaccharidosis multiple acyl-CoA dehydrogenase deficiency multiple myeloma myelitis myocardial infarction nephritis nephrosis nervous system disease neurodegenerative disease nutrition disease obesity obsolete Matthew-Wood syndrome obsolete type 1 diabetes mellitus 9 olfactory groove meningioma ovarian cancer ovarian carcinoma panic disorder parasagittal meningioma pituitary adenoma prediabetes syndrome progressive familial intrahepatic cholestasis 1 progressive muscular atrophy progressive supranuclear palsy protein-energy malnutrition psammomatous meningioma pyoureter renal osteodystrophy retrograde amnesia sarcoma secondary Parkinson disease secretory meningioma silent myocardial infarction situs inversus sphingolipidosis spinal meningioma spindle cell sarcoma tauopathy thalassemia transitional meningioma tricuspid valve stenosis trigonitis tuberous sclerosis 1 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 visual epilepsy
10723	solute carrier family 12 member 7	SLC12A7	Homo sapiens (human)
10721	DNA polymerase theta	POLQ	Homo sapiens (human)
10720	UDP glucuronosyltransferase family 2 member B11	UGT2B11	Homo sapiens (human)	cholangiocarcinoma intrahepatic cholangiocarcinoma prostate cancer prostate carcinoma
10718	neuregulin 3	NRG3	Homo sapiens (human)
10716	T-box brain transcription factor 1	TBR1	Homo sapiens (human)
10715	ceramide synthase 1	CERS1 Aliases: LAG1 UOG1	Homo sapiens (human)	Alzheimer's disease Crohn's colitis Crohn's disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Japanese encephalitis Unverricht-Lundborg syndrome arteriosclerotic cardiovascular disease atherosclerosis blepharospasm cancer central nervous system cancer congestive heart failure coronary artery disease dementia dengue disease dentatorubral-pallidoluysian atrophy double outlet right ventricle early myoclonic encephalopathy embryoma focal hand dystonia gliosarcoma hand, foot and mouth disease head and neck squamous cell carcinoma high grade glioma inflammatory bowel disease 1 inflammatory bowel disease intellectual disability learning disability malaria mixed glioma multiple types of congenital heart defects 6 neuroblastoma papillary adenocarcinoma papillary renal cell carcinoma primary spontaneous pneumothorax progressive myoclonus epilepsy 4 progressive myoclonus epilepsy 8 progressive myoclonus epilepsy steatotic liver disease tetralogy of Fallot thyroid gland papillary carcinoma ulcerative colitis viral infectious disease visceral heterotaxy visual epilepsy yellow fever
10714	DNA polymerase delta 3, accessory subunit	POLD3	Homo sapiens (human)
10713	ubiquitin specific peptidase 39	USP39	Homo sapiens (human)
10712	endosomal transmembrane epsin interactor 3	ENTREP3	Homo sapiens (human)

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