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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 **7851 - 7875** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
55802	decapping mRNA 1A	DCP1A Aliases: HSA275986 SMAD4IP1 SMIF	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
64421	DNA cross-link repair 1C	DCLRE1C	Homo sapiens (human)
54798	dachsous cadherin-related 2	DCHS2	Homo sapiens (human)
8642	dachsous cadherin-related 1	DCHS1	Homo sapiens (human)
117159	dermcidin	DCD	Homo sapiens (human)
1630	DCC netrin 1 receptor	DCC	Homo sapiens (human)
131566	discoidin, CUB and LCCL domain containing 2	DCBLD2	Homo sapiens (human)
285761	discoidin, CUB and LCCL domain containing 1	DCBLD1	Homo sapiens (human)
55827	DDB1 and CUL4 associated factor 6	DCAF6	Homo sapiens (human)
26094	DDB1 and CUL4 associated factor 4	DCAF4	Homo sapiens (human)
25879	DDB1 and CUL4 associated factor 13	DCAF13	Homo sapiens (human)
79269	DDB1 and CUL4 associated factor 10	DCAF10	Homo sapiens (human)
9730	DDB1 and CUL4 associated factor 1	DCAF1	Homo sapiens (human)
1629	dihydrolipoamide branched chain transacylase E2	DBT Aliases: BCKAD-E2 BCKDH-E2 BCOADC-E2 branched chain 2-oxo-acid dehydrogenase complex component E2 dihydrolipoyllysine-residue (2-methylpropanoyl)transferase lipoamide acyltransferase component of branched-chain alpha-keto acid dehydrogenase complex, mitochondrial	Homo sapiens (human)	acute pancreatitis autoimmune hepatitis borderline personality disorder brain edema breast cancer breast carcinoma cancer carcinoma cardiovascular system disease central nervous system cancer dilated cardiomyopathy 1A dilated cardiomyopathy dystonia eating disorder embryoma epilepsy focal hand dystonia generalized dystonia giant cell glioblastoma glioblastoma gliosarcoma heart disease high grade glioma hypoglycemia intellectual disability intermittent explosive disorder lactic acidosis learning disability maple syrup urine disease melanoma mixed glioma pancreatitis post-traumatic stress disorder primary biliary cholangitis skin melanoma substance abuse substance-related disorder syndromic X-linked intellectual disability 94 visual epilepsy
51163	debranching RNA lariats 1	DBR1	Homo sapiens (human)
28988	drebrin like	DBNL	Homo sapiens (human)
1627	drebrin 1	DBN1	Homo sapiens (human)
1622	diazepam binding inhibitor, acyl-CoA binding protein	DBI	Homo sapiens (human)
1621	dopamine beta-hydroxylase	DBH	Homo sapiens (human)
10926	DBF4-CDC7 kinase regulatory subunit	DBF4	Homo sapiens (human)
26528	DAZ associated protein 1	DAZAP1	Homo sapiens (human)
1616	death domain associated protein	DAXX	Homo sapiens (human)
199699	DAN domain BMP antagonist family member 5	DAND5	Homo sapiens (human)
747	diacylglycerol lipase alpha	DAGLA Aliases: DAGLALPHA KIAA0659 NSDDR neural stem cell-derived dendrite regulator	Homo sapiens (human)

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