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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 **417851 - 417875** of **422592** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
11060	WW domain containing E3 ubiquitin protein ligase 2	WWP2	Homo sapiens (human)
11057	abhydrolase domain containing 2, acylglycerol lipase	ABHD2	Homo sapiens (human)
11056	DExD-box helicase 52	DDX52	Homo sapiens (human)
11055	zona pellucida binding protein	ZPBP	Homo sapiens (human)
11054	opioid growth factor receptor	OGFR	Homo sapiens (human)
11052	cleavage and polyadenylation specific factor 6	CPSF6	Homo sapiens (human)
11047	ADRM1 26S proteasome ubiquitin receptor	ADRM1	Homo sapiens (human)
11046	solute carrier family 35 member D2	SLC35D2 Aliases: SQV7L UGTrel8	Homo sapiens (human)
11045	uroplakin 1A	UPK1A	Homo sapiens (human)
11044	terminal nucleotidyltransferase 4A	TENT4A	Homo sapiens (human)
11041	beta-1,4-glucuronyltransferase 1	B4GAT1 Aliases: B3GN-T1 BETA3GNTI IGnT N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase iGAT	Homo sapiens (human)	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome anencephaly 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 blindness breast cancer breast carcinoma cataract centronuclear myopathy coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy-dystroglycanopathy type A13 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy congenital myopathy 1A congenital myopathy 4A congenital structural myopathy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism distal myopathy facioscapulohumeral muscular dystrophy glaucoma hydranencephaly hydrocephalus hydronephrosis isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy lissencephaly megaconial type congenital muscular dystrophy microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 nemaline myopathy 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 pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal detachment rigid spine muscular dystrophy 1 rippling muscle disease 2 senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly syndromic X-linked intellectual disability Najm type
11037	stonin 1	STON1	Homo sapiens (human)
11035	receptor interacting serine/threonine kinase 3	RIPK3	Homo sapiens (human)
11033	ArfGAP with dual PH domains 1	ADAP1	Homo sapiens (human)
11031	RAB31, member RAS oncogene family	RAB31	Homo sapiens (human)
11027	leukocyte immunoglobulin like receptor A2	LILRA2	Homo sapiens (human)
11026	leukocyte immunoglobulin like receptor A3	LILRA3	Homo sapiens (human)
11024	leukocyte immunoglobulin like receptor A1	LILRA1	Homo sapiens (human)
11018	transmembrane p24 trafficking protein 1	TMED1 Aliases: IL1RL1LG Il1rl1l MGC1270 ST2L p24g1 p24gamma1	Homo sapiens (human)	acquired immunodeficiency syndrome breast cancer human immunodeficiency virus infectious disease
11016	activating transcription factor 7	ATF7	Homo sapiens (human)
11012	kallikrein related peptidase 11	KLK11	Homo sapiens (human)
11011	tousled like kinase 2	TLK2	Homo sapiens (human)
11009	interleukin 24	IL24	Homo sapiens (human)
11006	leukocyte immunoglobulin like receptor B4	LILRB4	Homo sapiens (human)
11001	solute carrier family 27 member 2	SLC27A2	Homo sapiens (human)

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