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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 **6701 - 6725** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
57007	atypical chemokine receptor 3	ACKR3	Homo sapiens (human)
57016	aldo-keto reductase family 1 member B10	AKR1B10 Aliases: AKR1B12 ALDRLn ARL-1 ARL1 HIS HSI aldo-keto reductase family 1, member B11 (aldose reductase-like) aldose reductase-like 1 aldose reductase-like peptide aldose reductase-related protein small intestine reductase	Homo sapiens (human)	Barrett's esophagus Burkitt lymphoma Schimke immuno-osseous dysplasia actinic keratosis acute pancreatitis adenocarcinoma adenoma adrenal cortex cancer adult respiratory distress syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bile duct adenocarcinoma bile duct carcinoma bladder carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ cholangiocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma contact dermatitis coronary artery disease cribriform carcinoma cystic fibrosis diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy embryoma endometrial cancer endometrial carcinoma esophageal cancer esophageal carcinoma esophagus adenocarcinoma esophagus squamous cell carcinoma follicular adenoma gallbladder disease gastrointestinal system cancer giant cell glioblastoma glioblastoma granular cell carcinoma hepatitis B hepatitis C hepatocellular carcinoma high grade glioma inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma large intestine cancer leprosy liver cancer liver carcinoma liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma melanoma microcystic adenoma microphthalmia nasopharynx carcinoma neurodegeneration with brain iron accumulation 2a neurodegeneration with brain iron accumulation 2b neurodegeneration with brain iron accumulation 3 neurodegeneration with brain iron accumulation 4 neurodegeneration with brain iron accumulation 5 neurodegeneration with brain iron accumulation 6 neurodegeneration with brain iron accumulation newborn respiratory distress syndrome nicotine dependence nodular prostate obsolete Matthew-Wood syndrome occupational dermatitis pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatitis pantothenate kinase-associated neurodegeneration papillary adenoma parapsoriasis primary immunodeficiency disease prostate cancer prostate carcinoma prostatic adenoma psoriasis pustulosis of palm and sole sarcomatoid carcinoma seborrheic keratosis skin disease skin melanoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis urinary bladder cancer uterine corpus cancer varicose veins
57017	coenzyme Q9	COQ9	Homo sapiens (human)
57018	cyclin L1	CCNL1	Homo sapiens (human)
57020	VPS35 endosomal protein sorting factor like	VPS35L	Homo sapiens (human)
57038	arginyl-tRNA synthetase 2, mitochondrial	RARS2	Homo sapiens (human)
57045	twisted gastrulation BMP signaling modulator 1	TWSG1	Homo sapiens (human)
57053	cholinergic receptor nicotinic alpha 10 subunit	CHRNA10	Homo sapiens (human)
57060	poly(rC) binding protein 4	PCBP4	Homo sapiens (human)
57082	kinetochore scaffold 1	KNL1	Homo sapiens (human)
57084	solute carrier family 17 member 6	SLC17A6	Homo sapiens (human)
57089	ectonucleoside triphosphate diphosphohydrolase 7	ENTPD7 Aliases: FLJ30978 LALP1	Homo sapiens (human)
57091	Cas scaffold protein family member 4	CASS4	Homo sapiens (human)
57092	PEST proteolytic signal containing nuclear protein	PCNP	Homo sapiens (human)
57094	carboxypeptidase A6	CPA6	Homo sapiens (human)
57095	PITH domain containing 1	PITHD1	Homo sapiens (human)
57097	poly(ADP-ribose) polymerase family member 11	PARP11 Aliases: ARTD11	Homo sapiens (human)	microcephaly viral infectious disease
57101	anoctamin 2	ANO2	Homo sapiens (human)
57103	TP53 induced glycolysis regulatory phosphatase	TIGAR Aliases: TP53-induced glycolysis and apoptosis regulator	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 Fanconi anemia complementation group A Fanconi anemia Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome T-cell acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute pancreatitis adult T-cell leukemia/lymphoma adult lymphoma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 anterior horn cell disease autosomal recessive distal hereditary motor neuronopathy 1 brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer central nervous system lymphoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease childhood leukemia childhood lymphoma chromophobe renal cell carcinoma chronic lymphocytic leukemia clear cell renal cell carcinoma cleft palate collecting duct carcinoma colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma degenerative disc disease dementia embryoma epilepsy esophagus squamous cell carcinoma familial retinoblastoma giant cell glioblastoma glioblastoma gliosarcoma hemiplegia hepatocellular carcinoma high grade glioma hypoglycemia inflammatory bowel disease 1 inflammatory bowel disease intestinal benign neoplasm intestinal cancer isolated cleft palate large intestine cancer lateral sclerosis leukemia liver cancer liver carcinoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma mixed glioma motor neuron disease nasopharynx carcinoma neurodegenerative disease nonpapillary renal cell carcinoma obesity obsolete ymphosarcoma pancreatitis papillary renal cell carcinoma primary cutaneous T-cell non-Hodgkin lymphoma renal carcinoma renal cell carcinoma retinoblastoma sarcomatoid renal cell carcinoma schizophrenia spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy stomach cancer stomach carcinoma trilateral retinoblastoma ulcerative colitis
57104	patatin like phospholipase domain containing 2	PNPLA2 Aliases: ATGL FP17548 TTS-2.2 desnutrin iPLA2zeta	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 Barth syndrome Chanarin-Dorfman syndrome Ehlers-Danlos syndrome Kuhnt-Junius degeneration Laron syndrome Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acanthosis nigricans achondroplasia acquired metabolic disease acute myocardial infarction acute promyelocytic leukemia adenocarcinoma adenoma adenosarcoma adult liposarcoma age related macular degeneration agnosia anogenital venereal wart arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal recessive congenital ichthyosis 1 bacterial sepsis bladder carcinoma bone disease bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiomyopathy cardiovascular system disease cartilage disease cavernous hemangioma celiac disease central nervous system cancer cerebral degeneration childhood liposarcoma childhood osteosarcoma cholecystitis chorioangioma chylomicron retention disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart cone-rod dystrophy congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital generalized lipodystrophy congestive heart failure connective tissue disease coronary artery disease coronary thrombosis cribriform carcinoma degeneration of macula and posterior pole depressive disorder developmental coordination disorder diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dysthymic disorder embryoma endometrial hyperplasia endomyocardial fibrosis epithelioid leiomyosarcoma exudative vitreoretinopathy 1 exudative vitreoretinopathy eye disease familial combined hyperlipidemia familial hyperlipidemia familial lipoprotein lipase deficiency familial periodic paralysis familial retinoblastoma fibromyalgia fundus albipunctatus gestational diabetes gliosarcoma glomus tumor glucose intolerance glycogen storage disease II granular cell carcinoma heart disease hemangioma hepatoblastoma hepatocellular carcinoma high grade glioma histiocytoid hemangioma hyperinsulinism hyperlipoproteinemia type V hypertrophic cardiomyopathy ichthyosis impotence intramuscular hemangioma isolated elevated serum creatine phosphokinase levels keratosis follicularis large intestine cancer leiomyosarcoma leukostasis lipoatrophic diabetes mellitus lipodystrophy liposarcoma liver cancer lung benign neoplasm lung cancer lung carcinoma lymphangioma macular degeneration major depressive disorder melancholic depression melanoma microphthalmia mixed glioma mongolian spot myocardial infarction myopathy myositis myxoid leiomyosarcoma nasopharynx carcinoma nephroblastoma neuropathy neurotic disorder nicotine dependence obesity obsolete Matthew-Wood syndrome obsolete congenital ichthyosiform erythroderma obsolete melancholia ocular melanoma osteogenesis imperfecta type 10 osteogenesis imperfecta type 11 osteogenesis imperfecta type 12 osteogenesis imperfecta type 13 osteogenesis imperfecta type 14 osteogenesis imperfecta type 15 osteogenesis imperfecta type 16 osteogenesis imperfecta type 17 osteogenesis imperfecta type 1 osteogenesis imperfecta type 2 osteogenesis imperfecta type 3 osteogenesis imperfecta type 4 osteogenesis imperfecta type 5 osteogenesis imperfecta type 6 osteogenesis imperfecta type 7 osteogenesis imperfecta type 8 osteogenesis imperfecta type 9 osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures osteogenesis imperfecta osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma peripheral nervous system disease pleomorphic liposarcoma polycystic ovary syndrome prediabetes syndrome premature ejaculation primary ciliary dyskinesia 1 primary ciliary dyskinesia proliferative diabetic retinopathy prostate cancer prostate carcinoma pseudoxanthoma elasticum psychologic dyspareunia rectal benign neoplasm rectum adenocarcinoma rectum cancer retinal disease retinitis pigmentosa retinitis retinoblastoma retinopathy of prematurity rhabdomyosarcoma rheumatoid arthritis schizophrenia sensorineural hearing loss silent myocardial infarction skin melanoma steatotic liver disease stomach cancer stomach carcinoma systemic primary carnitine deficiency disease trilateral retinoblastoma tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer
57105	cysteinyl leukotriene receptor 2	CYSLTR2	Homo sapiens (human)
57113	transient receptor potential cation channel subfamily C member 7	TRPC7	Homo sapiens (human)
57115	peptidoglycan recognition protein 4	PGLYRP4	Homo sapiens (human)
57117	integrator complex subunit 12	INTS12	Homo sapiens (human)
57118	calcium/calmodulin dependent protein kinase ID	CAMK1D	Homo sapiens (human)

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