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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

Search results for "response to monosaccharide"

Displaying entries **51 - 75** of **750** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
5208	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	PFKFB2	Homo sapiens (human)
5211	phosphofructokinase, liver type	PFKL	Homo sapiens (human)
5290	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	PIK3CA Aliases: PI3K	Homo sapiens (human)	CLOVES syndrome Cowden syndrome 5 breast angiosarcoma breast cancer cerebral cavernous malformation colon adenocarcinoma colorectal cancer colorectal carcinoma cutaneous Paget's disease epidermal nevus estrogen-receptor positive breast cancer hepatocellular carcinoma lung cancer ovarian cancer rectal benign neoplasm seborrheic keratosis stomach cancer
5313	pyruvate kinase L/R	PKLR	Homo sapiens (human)	Gaucher's disease congenital nonspherocytic hemolytic anemia 2 congenital nonspherocytic hemolytic anemia malaria type 2 diabetes mellitus
5465	peroxisome proliferator activated receptor alpha	PPARA	Homo sapiens (human)	Alzheimer's disease coronary artery disease hepatocellular carcinoma lipid metabolism disorder myocardial infarction
5467	peroxisome proliferator activated receptor delta	PPARD	Homo sapiens (human)	type 2 diabetes mellitus
5530	protein phosphatase 3 catalytic subunit alpha	PPP3CA	Homo sapiens (human)	developmental and epileptic encephalopathy 91
5562	protein kinase AMP-activated catalytic subunit alpha 1	PRKAA1	Homo sapiens (human)	Huntington's disease breast cancer colon cancer
5563	protein kinase AMP-activated catalytic subunit alpha 2	PRKAA2 Aliases: AMPK AMPKa2	Homo sapiens (human)	type 2 diabetes mellitus
5743	prostaglandin-endoperoxide synthase 2	PTGS2 Aliases: COX2 cyclooxygenase 2 prostaglandin G/H synthase 2	Homo sapiens (human)	arteriosclerosis asthma avian influenza cardiovascular system disease chronic obstructive pulmonary disease cystic fibrosis esophagitis hepatocellular carcinoma idiopathic pulmonary fibrosis liver cirrhosis lung non-small cell carcinoma myocardial infarction osteoarthritis pancreatic cancer prostate cancer pulmonary fibrosis rheumatoid arthritis sarcoidosis urinary bladder cancer
6198	ribosomal protein S6 kinase B1	RPS6KB1	Homo sapiens (human)
6434	transformer 2 beta homolog	TRA2B	Homo sapiens (human)
6443	sarcoglycan beta	SGCB	Homo sapiens (human)	autosomal recessive limb-girdle muscular dystrophy type 2E muscular dystrophy
6518	solute carrier family 2 member 5	SLC2A5	Homo sapiens (human)
6648	superoxide dismutase 2	SOD2	Homo sapiens (human)	Alzheimer's disease Kuhnt-Junius degeneration Leber hereditary optic neuropathy acute myeloid leukemia alcoholic liver cirrhosis asthma bilirubin metabolic disorder breast cancer cardiomyopathy carotid artery disease diabetic angiopathy dilated cardiomyopathy hepatocellular carcinoma hypertension inclusion body myositis infectious mononucleosis liver cirrhosis lung cancer metabolic dysfunction-associated steatohepatitis metabolic dysfunction-associated steatotic liver disease multiple myeloma neuronal ceroid lipofuscinosis optic neuritis osteoporosis ovarian cancer pancreatic cancer polyneuropathy primary open angle glaucoma pseudoxanthoma elasticum reactive arthritis stomach cancer systemic lupus erythematosus type 1 diabetes mellitus type 2 diabetes mellitus vitiligo
6720	sterol regulatory element binding transcription factor 1	SREBF1	Homo sapiens (human)	coronary artery disease disease of metabolism type 2 diabetes mellitus
6722	serum response factor	SRF	Homo sapiens (human)	cardiomyopathy lymphangioleiomyomatosis
7040	transforming growth factor beta 1	TGFB1	Homo sapiens (human)	Behcet's disease Camurati-Engelmann disease aphthous stomatitis aplastic anemia asthma atopic dermatitis berylliosis breast cancer chronic obstructive pulmonary disease colon adenocarcinoma cystic fibrosis eosinophilic esophagitis factor VIII deficiency inflammatory bowel disease lung disease multiple myeloma myocardial infarction osteochondrodysplasia pulmonary emphysema pulmonary fibrosis pulmonary hypertension pulmonary sarcoidosis renal cell carcinoma tracheal stenosis uveitis
7057	thrombospondin 1	THBS1	Homo sapiens (human)	cholangiocarcinoma pancreatic cancer pancreatic ductal carcinoma primary open angle glaucoma
7124	tumor necrosis factor	TNF	Homo sapiens (human)	Alzheimer's disease Behcet's disease Gaucher's disease Graves ophthalmopathy Graves' disease Kawasaki disease Sjogren's syndrome acne adult respiratory distress syndrome anterior uveitis aplastic anemia asthma atopic dermatitis bacterial pneumonia beta thalassemia breast adenocarcinoma breast cancer bronchopulmonary dysplasia cerebral infarction cervical cancer chorioamnionitis chronic obstructive pulmonary disease coronary artery disease coronary restenosis cystic fibrosis dermatitis herpetiformis dermatitis diabetic angiopathy diabetic retinopathy erythema nodosum esophagitis extrinsic allergic alveolitis farmer's lung hemochromatosis hepatitis B hepatocellular carcinoma hidradenitis suppurativa high grade glioma hypertension hypochromic microcytic anemia intermediate uveitis iron deficiency anemia leprosy liver disease low tension glaucoma lung non-small cell carcinoma malaria metabolic dysfunction and alcohol associated liver disease migraine without aura migraine mucocutaneous leishmaniasis multiple myeloma multiple sclerosis neutropenia obstructive sleep apnea open-angle glaucoma paracoccidioidomycosis pre-eclampsia primary open angle glaucoma prostate cancer psoriasis psoriatic arthritis pulmonary fibrosis pulmonary sarcoidosis pulmonary tuberculosis pustulosis of palm and sole renal cell carcinoma rheumatoid arthritis rhinitis schizophrenia scleritis sensorineural hearing loss silicosis skin disease systemic lupus erythematosus thrombocytopenia trachoma type 1 diabetes mellitus typhoid fever uveitis vascular dementia visceral leishmaniasis visual epilepsy
7351	uncoupling protein 2	UCP2	Homo sapiens (human)	carotid artery disease diabetic neuropathy end stage renal disease hypertension obesity
7392	upstream transcription factor 2, c-fos interacting	USF2	Homo sapiens (human)
7776	zinc finger protein 236	ZNF236	Homo sapiens (human)
8473	O-linked N-acetylglucosamine (GlcNAc) transferase	OGT Aliases: FLJ23071 HRNT1 MGC22921 O-GLCNAC OGT1 UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase	Homo sapiens (human)	non-syndromic X-linked intellectual disability 106
8660	insulin receptor substrate 2	IRS2	Homo sapiens (human)	type 2 diabetes mellitus

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