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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	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 **1 - 25** of **1582** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
109703458	hydroxyacyl-thioester dehydratase type 2	HTD2	Homo sapiens (human)	rheumatoid arthritis
100861540	CYP3A7-CYP3A51P readthrough	CYP3A7-CYP3A51P	Homo sapiens (human)	bronchus cancer bronchus carcinoma cancer embryoma lung cancer lung carcinoma
100528030	POC1B-GALNT4 readthrough	POC1B-GALNT4	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer
100507436	MHC class I polypeptide-related sequence A	MICA Aliases: PERB11.1	Homo sapiens (human)	Addison's disease 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 Barrett's esophagus Behcet's disease Brucella melitensis brucellosis Burkitt lymphoma Crohn's colitis Crohn's disease Evans' syndrome Goodpasture syndrome Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Japanese encephalitis Meniere's disease Pick's disease Reye syndrome Schwartz-Jampel syndrome 1 St. Louis encephalitis Stevens-Johnson syndrome Takayasu's arteritis X-linked dilated cardiomyopathy acquired immunodeficiency syndrome acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adrenal cortical hypofunction allergic disease alveolar echinococcosis amyloidosis ankylosing spondylitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura azoospermia basal cell carcinoma bone osteosarcoma breast cancer breast carcinoma breast fibrocystic disease bronchiectasis bronchus cancer bronchus carcinoma brucellosis cancer carcinoma cardiovascular system disease celiac disease central nervous system cancer cerebral degeneration cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood leukemia childhood osteosarcoma cholecystolithiasis choledocholithiasis cholelithiasis chromophobe renal cell carcinoma chronic kidney disease chronic myeloid leukemia ciliary body disease clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer common wart complex partial epilepsy coronary aneurysm coronary artery disease coronary thrombosis cribriform carcinoma dengue disease dengue hemorrhagic fever denture stomatitis diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy disease of mental health distal arthrogryposis embryoma endolymphatic hydrops enterobiasis epilepsy esophagus squamous cell carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis familial mediterranean fever familial retinoblastoma gallbladder disease gastrointestinal system disease gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma granulomatosis with polyangiitis head and neck cancer head and neck squamous cell carcinoma heart disease hematologic cancer hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease idiopathic interstitial pneumonia idiopathic pulmonary fibrosis immune system disease inflammatory bowel disease 1 inflammatory bowel disease intestinal disease intestinal schistosomiasis iris disease islet cell tumor kidney cancer large intestine cancer leech infestation leprosy leukemia leukoencephalopathy with vanishing white matter liver cancer liver carcinoma liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma malignant conjunctival melanoma maxillary sinus squamous cell carcinoma melanoma mevalonic aciduria microglandular adenosis mixed glioma multiple epiphyseal dysplasia multiple myeloma multiple sclerosis myiasis myocardial infarction nasopharynx carcinoma neuroblastoma nonpapillary renal cell carcinoma obsolete type 1 diabetes mellitus 9 oral submucous fibrosis osteochondrodysplasia osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma panuveitis papillary renal cell carcinoma parapsoriasis pneumonia polyarteritis nodosa primary immunodeficiency disease primary sclerosing cholangitis prostate cancer prostate carcinoma psoriasis psoriatic arthritis psychotic disorder pustulosis of palm and sole rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma respiratory syncytial virus infectious disease retinoblastoma rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma schistosomiasis sclerosing cholangitis sebaceous carcinoma silent myocardial infarction skin benign neoplasm skin cancer skin carcinoma skin melanoma spondylitis spondyloarthropathy spondylosis squamous cell carcinoma squamous cell neoplasm stomach cancer stomach carcinoma stomatitis sweat gland cancer systemic lupus erythematosus temporal arteritis temporal lobe epilepsy thromboangiitis obliterans thymic carcinoma thymoma thyroid adenoma thyroid cancer thyroid gland carcinoma tongue squamous cell carcinoma toxoplasmosis trichinosis trilateral retinoblastoma 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 ulcerative colitis ulcerative stomatitis uveal melanoma uveitis vasculitis viral infectious disease visual epilepsy yellow fever
100137049	phospholipase A2 group IVB	PLA2G4B Aliases: HsT16992 cPLA2-beta	Homo sapiens (human)	head and neck squamous cell carcinoma schizophrenia
100131187	thiosulfate sulfurtransferase like domain containing 1	TSTD1	Homo sapiens (human)
730249	aconitate decarboxylase 1	ACOD1 Aliases: CAD	Homo sapiens (human)	bacterial sepsis central nervous system cancer gliosarcoma hepatitis B high grade glioma lung disease mixed glioma peripheral artery disease viral infectious disease
729920	CDP-L-ribitol pyrophosphorylase A	CRPPA Aliases: 4-diphosphocytidyl-2C-methyl-D-erythritol synthase homolog (Arabidopsis) D-ribitol-5-phosphate cytidylyltransferase IspD Nip hCG_1745121 notch1-induced protein	Homo sapiens (human)	Axenfeld-Rieger syndrome Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome agnosia anemia 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 bilateral optic nerve hypoplasia cataract chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy-dystroglycanopathy A7 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A8 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism developmental coordination disorder distal myopathy epilepsy facioscapulohumeral muscular dystrophy familial periodic paralysis fibromyalgia fundus dystrophy glaucoma hydranencephaly hydrocephalus intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly macrocytic anemia microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myositis nonpapillary renal cell carcinoma 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 obstructive hydrocephalus oculopharyngeal muscular dystrophy optic atrophy papillary renal cell carcinoma persistent hyperplastic primary vitreous pneumonia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion renal carcinoma renal cell carcinoma retinal detachment rippling muscle disease 2 sarcomatoid renal cell carcinoma scoliosis senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly syndromic X-linked intellectual disability Najm type visual epilepsy
729238	surfactant protein A2	SFTPA2 Aliases: COLEC5 SP-A2 surfactant, pulmonary-associated protein A2A	Homo sapiens (human)	Zollinger-Ellison syndrome acute interstitial pneumonia adenocarcinoma adenoid hypertrophy adenoma adult respiratory distress syndrome allergic asthma allergic bronchopulmonary aspergillosis allergic rhinitis ankylosing spondylitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis bacterial pneumonia bacterial sepsis bronchiectasis bronchiolo-alveolar adenocarcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease cataract 32 multiple types chronic obstructive pulmonary disease communicating hydrocephalus congenital diaphragmatic hernia congenital heart disease corneal ulcer coronary artery disease craniosynostosis cribriform carcinoma cystic fibrosis embryoma esophagitis gastroesophageal reflux disease granular cell carcinoma heart disease hydrocephalus hypereosinophilic syndrome hyperinsulinism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis interstitial lung disease interstitial nephritis intrinsic asthma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lymphangioleiomyomatosis newborn respiratory distress syndrome obesity obstructive hydrocephalus obstructive lung disease otitis media peptic esophagitis pneumocystosis pneumonia postinflammatory pulmonary fibrosis primary pulmonary hypertension prostate cancer prostate carcinoma psoriatic arthritis pulmonary fibrosis pulmonary tuberculosis pulmonary valve insufficiency pyelitis pyelonephritis respiratory failure respiratory syncytial virus infectious disease rheumatoid arthritis secondary hypertrophic osteoarthropathy senile degeneration of brain spondyloarthropathy spondylosis squamous cell carcinoma tongue squamous cell carcinoma tuberculosis tuberculous pneumothorax tubular adenocarcinoma urinary tract obstruction vasomotor rhinitis
729201	sperm acrosome associated 5B	SPACA5B Aliases: LYZL5B	Homo sapiens (human)
729020	ribulose-5-phosphate-3-epimerase like 1	RPEL1	Homo sapiens (human)
728819	C1GALT1 specific chaperone 1 like	C1GALT1C1L	Homo sapiens (human)
728661	solute carrier family 35 member E2B	SLC35E2B	Homo sapiens (human)
727936	glucoside xylosyltransferase 2	GXYLT2	Homo sapiens (human)
654346	galectin 9C	LGALS9C	Homo sapiens (human)	cancer
653509	surfactant protein A1	SFTPA1 Aliases: COLEC4 SP-A SP-A1 surfactant, pulmonary-associated protein A1A	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 Hermansky-Pudlak syndrome Pick's disease Reye syndrome T cell deficiency X-linked dominant hypophosphatemic rickets Zollinger-Ellison syndrome acute interstitial pneumonia adenocarcinoma adenoid hypertrophy adenoma adult respiratory distress syndrome allergic asthma allergic bronchopulmonary aspergillosis allergic rhinitis amnestic disorder amyloidosis anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis bacterial pneumonia bacterial sepsis bronchiectasis bronchiolitis obliterans bronchiolitis bronchopulmonary dysplasia bronchus cancer bronchus carcinoma cancer cardiovascular system disease cataract 32 multiple types cerebral degeneration cerebral infarction cerebrovascular disease chronic ethmoiditis chronic kidney disease chronic myeloid leukemia chronic obstructive pulmonary disease chronic sphenoidal sinusitis communicating hydrocephalus congenital diaphragmatic hernia congenital heart disease corneal disease corneal ulcer coronary artery disease craniosynostosis cribriform carcinoma cryptogenic organizing pneumonia cystic fibrosis diabetes mellitus diabetic ketoacidosis embryoma esophagitis essential thrombocythemia extrinsic allergic alveolitis familial periodic paralysis gastroesophageal reflux disease granular cell carcinoma heart disease hematologic cancer hydrocephalus hyperinsulinism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inflammatory bowel disease interstitial lung disease interstitial nephritis intrinsic asthma keratoconus liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lymphangioleiomyomatosis macrocytic anemia mastitis myelodysplastic syndrome myopathy neurodegenerative disease newborn respiratory distress syndrome obesity obsolete T lymphocyte deficiency obstructive hydrocephalus obstructive lung disease osteomalacia otitis media peptic esophagitis pneumocystosis pneumonia postinflammatory pulmonary fibrosis pulmonary alveolar proteinosis pulmonary edema pulmonary fibrosis pulmonary sarcoidosis pulmonary tuberculosis pulmonary valve insufficiency pyelitis pyelonephritis respiratory syncytial virus infectious disease retrograde amnesia rickets secondary hypertrophic osteoarthropathy senile degeneration of brain shigellosis sinusitis squamous cell carcinoma staphyloenterotoxemia systolic heart failure tongue squamous cell carcinoma tuberculosis tuberculous pneumothorax tubular adenocarcinoma urinary tract obstruction vasomotor rhinitis viral infectious disease
653308	N-acylsphingosine amidohydrolase 2B	ASAH2B Aliases: ASAH2L bA449O16.3 bA98I6.3	Homo sapiens (human)	breast cancer breast carcinoma
648791	protein phosphatase 1 regulatory subunit 3G	PPP1R3G	Homo sapiens (human)	obesity steatotic liver disease
646000	solute carrier family 35 member G4	SLC35G4	Homo sapiens (human)
644974	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase like 2	ALG1L2	Homo sapiens (human)	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
643664	solute carrier family 35 member G6	SLC35G6	Homo sapiens (human)
641371	acyl-CoA thioesterase 1	ACOT1 Aliases: ACH2 CTE-1 LACH2	Homo sapiens (human)	gastric adenocarcinoma hepatocellular carcinoma liver cancer
606495	cytochrome b5 reductase like	CYB5RL Aliases: LOC606495	Homo sapiens (human)
574537	UDP glucuronosyltransferase family 2 member A2	UGT2A2	Homo sapiens (human)	ovarian cancer ovarian carcinoma
497190	C-type lectin domain family 18 member B	CLEC18B	Homo sapiens (human)	acquired immunodeficiency syndrome cancer embryoma giant cell glioblastoma glioblastoma high grade glioma

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