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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 **415276 - 415300** of **422592** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
22992	lysine demethylase 2A	KDM2A	Homo sapiens (human)
22990	pecanex 1	PCNX1	Homo sapiens (human)
22989	myosin heavy chain 15	MYH15	Homo sapiens (human)
22987	synaptic vesicle glycoprotein 2C	SV2C	Homo sapiens (human)
22986	sortilin related VPS10 domain containing receptor 3	SORCS3	Homo sapiens (human)
22985	apoptotic chromatin condensation inducer 1	ACIN1	Homo sapiens (human)
22984	programmed cell death 11	PDCD11	Homo sapiens (human)
22983	microtubule associated serine/threonine kinase 1	MAST1	Homo sapiens (human)
22982	disco interacting protein 2 homolog C	DIP2C	Homo sapiens (human)
22979	EFR3 homolog B	EFR3B	Homo sapiens (human)
22976	PAX interacting protein 1	PAXIP1	Homo sapiens (human)
22974	TPX2 microtubule nucleation factor	TPX2	Homo sapiens (human)
22955	Scm polycomb group protein homolog 1	SCMH1	Homo sapiens (human)
22953	purinergic receptor P2X 2	P2RX2	Homo sapiens (human)
22950	solute carrier family 4 member 1 adaptor protein	SLC4A1AP	Homo sapiens (human)
22943	dickkopf WNT signaling pathway inhibitor 1	DKK1	Homo sapiens (human)
22941	SH3 and multiple ankyrin repeat domains 2	SHANK2	Homo sapiens (human)
22938	SNW domain containing 1	SNW1	Homo sapiens (human)
22937	SREBF chaperone	SCAP	Homo sapiens (human)
22936	elongation factor for RNA polymerase II 2	ELL2	Homo sapiens (human)
22934	ribose 5-phosphate isomerase A	RPIA	Homo sapiens (human)	Chagas disease agnosia cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital nystagmus critical illness polyneuropathy disease of metabolism dissociated nystagmus epilepsy familial adenomatous polyposis 1 familial adenomatous polyposis hepatocellular carcinoma inflammatory and toxic neuropathy islet cell tumor large intestine cancer liver cancer liver carcinoma meningoencephalitis multiple myeloma neuropathy optic atrophy papillary adenocarcinoma papillary renal cell carcinoma pathologic nystagmus peripheral nervous system disease polyneuropathy spontaneous ocular nystagmus thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma thyroid gland papillary carcinoma trypanosomiasis visual epilepsy
22933	sirtuin 2	SIRT2	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 Chagas disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Loeffler syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Rett syndrome Reye syndrome Richter's syndrome Werner syndrome abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction acute pancreatitis adenocarcinoma adenoma allergic asthma alternating hemiplegia of childhood amyotrophic lateral sclerosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autonomic neuropathy 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 bacterial infectious disease bacterial sepsis basal cell carcinoma bile duct adenocarcinoma bile duct carcinoma bladder carcinoma brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease central nervous system cancer central nervous system disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cholangiocarcinoma chromophobe renal cell carcinoma chronic apical periodontitis chronic lymphocytic leukemia chronic obstructive pulmonary disease clear cell renal cell carcinoma cocaine dependence collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis cribriform carcinoma cystic fibrosis degenerative disc disease dementia depressive disorder diabetes mellitus diabetic ketoacidosis distal arthrogryposis distal myopathy dysthymic disorder embryoma endometrial cancer endometrial carcinoma eosinophilic pneumonia epithelioid sarcoma essential hypertension facioscapulohumeral muscular dystrophy gastritis gastrointestinal system cancer giant cell glioblastoma glioblastoma gliosarcoma glucose intolerance granular cell carcinoma heart disease hepatitis B hepatitis hepatocellular carcinoma high grade glioma hyperglycemia hypertension inclusion body myositis intermittent claudication intrahepatic cholangiocarcinoma intrinsic asthma large intestine cancer leukemia limb-girdle muscular dystrophy listeriosis liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder melancholic depression melanoma metabolic dysfunction-associated steatotic liver disease middle cerebral artery infarction mixed glioma mood disorder multiple sclerosis muscular dystrophy myocardial infarction nasopharynx carcinoma nervous system disease neurodegenerative disease neurofibromatosis neurotic disorder nonpapillary renal cell carcinoma 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 obsolete melancholia obsolete type 1 diabetes mellitus 9 oculopharyngeal muscular dystrophy osteoarthritis osteoporosis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatitis papillary renal cell carcinoma periapical granuloma periapical periodontitis placental insufficiency prediabetes syndrome primary cutaneous T-cell non-Hodgkin lymphoma progeria progressive muscular atrophy prolymphocytic leukemia prostate cancer prostate carcinoma pulmonary embolism pulmonary eosinophilia renal carcinoma renal cell carcinoma rhabdomyosarcoma sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma secondary Parkinson disease silent myocardial infarction skin benign neoplasm skin cancer skin melanoma spindle cell sarcoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma synovial sarcoma tongue squamous cell carcinoma trypanosomiasis tuberculosis tubular adenocarcinoma 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 urethral obstruction urinary bladder cancer uterine corpus cancer vestibular schwannomatosis
22929	selenophosphate synthetase 1	SEPHS1	Homo sapiens (human)
22927	hyaluronan binding protein 4	HABP4 Aliases: IHABP4 SERBP1L	Homo sapiens (human)	Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma
22926	activating transcription factor 6	ATF6	Homo sapiens (human)

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