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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 **601 - 625** of **423164** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
1234	C-C motif chemokine receptor 5	CCR5	Homo sapiens (human)	Behcet's disease Kawasaki disease Sjogren's syndrome West Nile fever asthma berylliosis breast cancer cutaneous leishmaniasis fallopian tube disease gallbladder cancer granulomatosis with polyangiitis hepatitis B hepatitis C human immunodeficiency virus infectious disease hypertension juvenile rheumatoid arthritis multiple sclerosis posterior uveitis pulmonary sarcoidosis respiratory syncytial virus infectious disease rheumatoid arthritis sarcoidosis type 1 diabetes mellitus 22 urticaria
1235	C-C motif chemokine receptor 6	CCR6	Homo sapiens (human)
1236	C-C motif chemokine receptor 7	CCR7	Homo sapiens (human)
1238	atypical chemokine receptor 2	ACKR2	Homo sapiens (human)
1240	chemerin chemokine-like receptor 1	CMKLR1	Homo sapiens (human)
1241	leukotriene B4 receptor	LTB4R	Homo sapiens (human)
1244	ATP binding cassette subfamily C member 2	ABCC2	Homo sapiens (human)	Dubin-Johnson syndrome acute lymphoblastic leukemia bilirubin metabolic disorder cholangiocarcinoma chronic myeloid leukemia drug-induced hepatitis lung non-small cell carcinoma metabolic dysfunction-associated steatotic liver disease
1258	cyclic nucleotide gated channel subunit beta 1	CNGB1	Homo sapiens (human)	retinitis pigmentosa 45 retinitis pigmentosa
1259	cyclic nucleotide gated channel subunit alpha 1	CNGA1	Homo sapiens (human)	retinitis pigmentosa 49 retinitis pigmentosa
1261	cyclic nucleotide gated channel subunit alpha 3	CNGA3	Homo sapiens (human)	achromatopsia 2 color blindness
1263	polo like kinase 3	PLK3	Homo sapiens (human)
1265	calponin 2	CNN2	Homo sapiens (human)
1266	calponin 3	CNN3	Homo sapiens (human)
1268	cannabinoid receptor 1	CNR1	Homo sapiens (human)	obesity schizophrenia type 2 diabetes mellitus
1269	cannabinoid receptor 2	CNR2	Homo sapiens (human)
1271	ciliary neurotrophic factor receptor	CNTFR	Homo sapiens (human)
1272	contactin 1	CNTN1 Aliases: F3 GP135 glycoprotein gP135	Homo sapiens (human)	Compton-North congenital myopathy
1277	collagen type I alpha 1 chain	COL1A1	Homo sapiens (human)	Caffey disease Ehlers-Danlos syndrome arthrochalasia type 1 aggressive periodontitis beta thalassemia cutaneous leishmaniasis degenerative disc disease dentinogenesis imperfecta dermatofibrosarcoma protuberans osteogenesis imperfecta type 1 osteogenesis imperfecta type 2 osteogenesis imperfecta type 3 osteogenesis imperfecta type 4 osteogenesis imperfecta osteoporosis otosclerosis
1278	collagen type I alpha 2 chain	COL1A2	Homo sapiens (human)	Ehlers-Danlos syndrome arthrochalasia type 2 Ehlers-Danlos syndrome cardiac valvular type Ehlers-Danlos syndrome heart valve disease intracranial aneurysm osteogenesis imperfecta type 2 osteogenesis imperfecta type 3 osteogenesis imperfecta type 4 osteogenesis imperfecta osteoporosis
1280	collagen type II alpha 1 chain	COL2A1	Homo sapiens (human)	Kniest dysplasia Legg-Calve-Perthes disease Stickler syndrome 1 Stickler syndrome Torrance type platyspondylic dysplasia achondrogenesis type II chondrosarcoma chorioretinitis cleft palate eye disease multiple epiphyseal dysplasia with myopia and deafness myopia osteoarthritis osteochondrodysplasia osteonecrosis retinal detachment spondyloarthropathy spondyloepimetaphyseal dysplasia, Strudwick type spondyloepiphyseal dysplasia Stanescu type spondyloepiphyseal dysplasia congenita spondyloperipheral dysplasia
1281	collagen type III alpha 1 chain	COL3A1	Homo sapiens (human)	Ehlers-Danlos syndrome hypermobility type Ehlers-Danlos syndrome end stage renal disease vascular type Ehlers-Danlos syndrome
1282	collagen type IV alpha 1 chain	COL4A1	Homo sapiens (human)	brain small vessel disease 1 myocardial infarction retinal arterial tortuosity uterine fibroid
1284	collagen type IV alpha 2 chain	COL4A2	Homo sapiens (human)	atherosclerosis brain small vessel disease 2 porencephaly uterine fibroid
1285	collagen type IV alpha 3 chain	COL4A3	Homo sapiens (human)	Alport syndrome autosomal dominant Alport syndrome autosomal recessive Alport syndrome benign familial hematuria end stage renal disease
1286	collagen type IV alpha 4 chain	COL4A4	Homo sapiens (human)	autosomal recessive Alport syndrome benign familial hematuria end stage renal disease

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