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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 **7776 - 7800** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
845	calsequestrin 2	CASQ2	Homo sapiens (human)
2625	GATA binding protein 3	GATA3	Homo sapiens (human)
6444	sarcoglycan delta	SGCD	Homo sapiens (human)
417	ADP-ribosyltransferase 1	ART1 Aliases: ART2 ARTC1 CD296	Homo sapiens (human)	arthritis arthropathy astigmatism cancer central nervous system cancer colon carcinoma colorectal cancer colorectal carcinoma embryoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis hepatocellular carcinoma high grade glioma kidney disease large intestine cancer liver cancer mixed glioma nasopharynx carcinoma nephritis pancreatic cancer pancreatic carcinoma squamous cell carcinoma tongue squamous cell carcinoma tuberculosis
26097	chromatin target of PRMT1	CHTOP	Homo sapiens (human)
7358	UDP-glucose 6-dehydrogenase	UGDH Aliases: GDH UDP-GlcDH UDPGDH UGD uridine-diphospho glucose dehydrogenase	Homo sapiens (human)	Graves' disease Laron syndrome Zollinger-Ellison syndrome achondroplasia beta thalassemia breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cholangiocarcinoma developmental and epileptic encephalopathy 84 diarrhea enophthalmos giant cell glioblastoma giardiasis glioblastoma hepatocellular carcinoma high grade glioma hyperinsulinism hyperthyroidism hypoglycemia intrahepatic cholangiocarcinoma liver cancer lung benign neoplasm lung cancer lung carcinoma obsolete exophthalmos orbital disease peripheral artery disease placental insufficiency primary hyperoxaluria thalassemia thyrotoxicosis
8692	hyaluronidase 2	HYAL2 Aliases: LUCA2 LuCa-2 PH-20 homolog lysosomal hyaluronidase	Homo sapiens (human)	B-cell lymphoma acute chest syndrome adenocarcinoma adenoma adult lymphoma arthritis arthropathy breast cancer breast carcinoma bronchiolo-alveolar adenocarcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer central nervous system lymphoma childhood lymphoma colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital heart disease cribriform carcinoma dysplastic nevus syndrome embryoma endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis gastroenteritis gliosarcoma granular cell carcinoma high grade glioma ileitis ileocolitis inflammatory bowel disease large intestine cancer lung benign neoplasm lung cancer lung carcinoma lung small cell carcinoma lymphoma melanoma microphthalmia mixed glioma mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IX mucopolysaccharidosis VI mucopolysaccharidosis obsolete Matthew-Wood syndrome obsolete ymphosarcoma osteoarthritis primary pulmonary hypertension pulmonary hypertension reticulosarcoma rheumatoid arthritis sarcomatoid carcinoma skin melanoma squamous cell carcinoma tongue squamous cell carcinoma tubular adenocarcinoma uterine corpus cancer
6583	solute carrier family 22 member 4	SLC22A4	Homo sapiens (human)
390072	olfactory receptor family 52 subfamily N member 4	OR52N4	Homo sapiens (human)
1943	ephrin A2	EFNA2 Aliases: ELF-1 EPH-related receptor tyrosine kinase ligand 6 LERK6	Homo sapiens (human)	acute myeloid leukemia breast cancer breast carcinoma cancer cervical adenocarcinoma cervical cancer cervix carcinoma chronic granulomatous disease embryoma endometrial cancer endometrial carcinoma familial retinoblastoma gastrointestinal system cancer giant cell glioblastoma glioblastoma high grade glioma lupus erythematosus nasopharynx carcinoma nodular prostate pancreatic cancer pancreatic carcinoma prostate cancer prostate carcinoma prostatic adenoma retinoblastoma stomach cancer stomach carcinoma systemic lupus erythematosus trilateral retinoblastoma uterine corpus cancer
2900	glutamate ionotropic receptor kainate type subunit 4	GRIK4	Homo sapiens (human)
9671	WSC domain containing 2	WSCD2	Homo sapiens (human)
148003	galectin 16	LGALS16	Homo sapiens (human)	congestive heart failure diffuse large B-cell lymphoma thyroid adenoma thyroid cancer thyroid gland carcinoma
2641	glucagon	GCG	Homo sapiens (human)	Alzheimer's disease prediabetes syndrome
5304	prolactin induced protein	PIP	Homo sapiens (human)
163479	fibronectin type III domain containing 7	FNDC7	Homo sapiens (human)
10048	RAN binding protein 9	RANBP9	Homo sapiens (human)
28513	cadherin 19	CDH19	Homo sapiens (human)
2742	glycine receptor alpha 2	GLRA2	Homo sapiens (human)
1634	decorin	DCN Aliases: DSPG2 SLRR1B decorin proteoglycan	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 CADASIL 1 CADASIL Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Duchenne muscular dystrophy Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome Hailey-Hailey disease IgA glomerulonephritis Kaposi's sarcoma Li-Fraumeni syndrome 1 Li-Fraumeni syndrome Lyme disease Marfan syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Peyronie's disease Pick's disease Prader-Willi syndrome Reye syndrome Richter's syndrome Robinow syndrome Rothmund-Thomson syndrome SADDAN Seckel syndrome Silver-Russell syndrome Werner syndrome X-linked Aarskog syndrome abdominal aortic aneurysm achondrogenesis type IB achondroplasia actinic keratosis acute interstitial pneumonia acute myocardial infarction adult respiratory distress syndrome allergic asthma alopecia amyloidosis angiokeratoma angiosarcoma angle-closure glaucoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis atrophic gastritis autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa 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 dominant polycystic kidney disease autosomal recessive Robinow syndrome autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB 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 balanitis xerotica obliterans basal cell carcinoma benign breast phyllodes tumor bladder carcinoma bladder neck obstruction bone disease bone giant cell tumor bone osteosarcoma brain cancer breast cancer breast carcinoma breast fibroadenoma breast fibrocystic disease breast malignant phyllodes tumor breast metaplastic carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cardiovascular system disease cartilage disease central nervous system cancer cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cherubism childhood angiosarcoma childhood osteosarcoma cholestasis chondrodysplasia-pseudohermaphroditism syndrome chondrosarcoma chromophobe renal cell carcinoma chronic closed-angle glaucoma chronic interstitial cystitis chronic lymphocytic leukemia chronic obstructive pulmonary disease chronic ulcer of skin clear cell renal cell carcinoma collagen disease collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital diaphragmatic hernia congenital disorder of glycosylation congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy congenital stromal corneal dystrophy congestive heart failure connective tissue disease cornea plana corneal neovascularization coronary artery disease coronary thrombosis crescentic glomerulonephritis cutis laxa cystic fibrosis diabetes mellitus diabetic ketoacidosis distal myopathy embryoma endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis endomyocardial fibrosis epidermolysis bullosa dystrophica epithelioid malignant peripheral nerve sheath tumor epithelioid sarcoma esophageal cancer esophageal carcinoma essential hypertension exostosis facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy familial adenomatous polyposis familial periodic paralysis female stress incontinence gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glucose intolerance heart disease hepatocellular carcinoma hiatus hernia high grade glioma hyperglycemia hypertension hypertrophic cardiomyopathy hypochondroplasia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inclusion body myositis intellectual disability interstitial cystitis interstitial nephritis intestinal benign neoplasm intestinal cancer intrinsic asthma invasive ductal carcinoma kidney disease kidney failure kidney hypertrophy large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal disease larynx cancer learning disability limb-girdle muscular dystrophy lipoma liver cancer liver carcinoma liver cirrhosis localized scleroderma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma mal de Meleda malignant peripheral nerve sheath tumor mesangial proliferative glomerulonephritis microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microglandular adenosis mixed glioma multiple myeloma multiple sclerosis multiple symmetric lipomatosis muscular dystrophy myeloproliferative disorder with eosinophilia myocardial infarction myocarditis myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia myxofibrosarcoma neovascular inflammatory vitreoretinopathy nephritis nephrosclerosis nephrosis neurilemmoma neuroblastoma neurofibrosarcoma neurogenic arthropathy newborn respiratory distress syndrome 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 type 1 diabetes mellitus 9 oculopharyngeal muscular dystrophy ossification of the posterior longitudinal ligament of spine osteoarthritis osteochondrodysplasia 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 papillary adenocarcinoma papillary renal cell carcinoma papilloma periarthritis placental insufficiency pleomorphic lipoma polycystic kidney disease 1 polycystic ovary syndrome posterior amorphous corneal dystrophy postinflammatory pulmonary fibrosis prediabetes syndrome primary angle-closure glaucoma primary open angle glaucoma primary pulmonary hypertension progeria prostate cancer prostate carcinoma proteinuria pseudoachondroplasia pseudosarcomatous fibromatosis pulmonary fibrosis pulmonary hypertension pyelitis pyelonephritis pyoureter rapidly progressive glomerulonephritis recessive dystrophic epidermolysis bullosa renal carcinoma renal cell carcinoma renal infectious disease restrictive dermopathy retinal disease retinitis rippling muscle disease 2 sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma scleroderma seborrheic keratosis silent myocardial infarction situs inversus skin atrophy skin disease spindle cell sarcoma squamous cell carcinoma squamous cell papilloma steatotic liver disease stomach cancer stomach carcinoma systemic scleroderma tendinitis thrombosis thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma tracheal disease transitional cell carcinoma 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 uremia urinary bladder cancer uterine corpus cancer vascular cancer vascular disease vulva carcinoma vulvar dystrophy
56109	protocadherin gamma subfamily A, 6	PCDHGA6	Homo sapiens (human)
283159	olfactory receptor family 8 subfamily D member 1	OR8D1	Homo sapiens (human)
390037	olfactory receptor family 52 subfamily I member 1	OR52I1	Homo sapiens (human)
10765	lysine demethylase 5B	KDM5B	Homo sapiens (human)
55184	double zinc ribbon and ankyrin repeat domains 1	DZANK1	Homo sapiens (human)

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