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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

Search results for "monosaccharide binding"

Displaying entries **126 - 150** of **3910** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
56401	prolyl 3-hydroxylase 1	P3h1	Mus musculus (house mouse)
56421	phosphofructokinase, platelet	Pfkp	Mus musculus (house mouse)	disease of metabolism glycogen storage disease
56485	solute carrier family 2 (facilitated glucose transporter), member 5	Slc2a5	Mus musculus (house mouse)
56620	C-type lectin domain family 4, member n	Clec4n	Mus musculus (house mouse)
60416	phosphofructokinase, platelet	Pfkp	Rattus norvegicus (Norway rat)	disease of metabolism glycogen storage disease
64035	glycogen phosphorylase L	Pygl	Rattus norvegicus (Norway rat)	glycogen storage disease VI glycogen storage disease lactic acidosis
64175	prolyl 3-hydroxylase 1	P3H1	Homo sapiens (human)
64475	prolyl 4-hydroxylase subunit alpha 1	P4ha1	Rattus norvegicus (Norway rat)
65152	phosphofructokinase, muscle	Pfkm	Rattus norvegicus (Norway rat)	disease of metabolism glycogen storage disease VII glycogen storage disease
65197	solute carrier family 2 member 5	Slc2a5	Rattus norvegicus (Norway rat)
66171	6-phosphogluconolactonase	Pgls	Mus musculus (house mouse)
66179	2-oxoglutarate and iron-dependent oxygenase domain containing 3	Ogfod3	Mus musculus (house mouse)
66646	ribulose-5-phosphate-3-epimerase	Rpe	Mus musculus (house mouse)
66890	lectin, mannose-binding 2	Lman2	Mus musculus (house mouse)
69064	fucose mutarotase	Fuom	Mus musculus (house mouse)
69165	CD209b antigen	Cd209b	Mus musculus (house mouse)
70361	lectin, mannose-binding, 1	Lman1	Mus musculus (house mouse)
73149	C-type lectin domain family 4, member a3	Clec4a3	Mus musculus (house mouse)
74443	prolyl 4-hydroxylase, transmembrane (endoplasmic reticulum)	P4htm	Mus musculus (house mouse)
75863	C-type lectin domain family 4, member g	Clec4g	Mus musculus (house mouse)
78989	collectin subfamily member 11	COLEC11 Aliases: CL-11 CL-K1 Collectin K1 MGC3279	Homo sapiens (human)	3MC syndrome 1 3MC syndrome 2 3MC syndrome 3 3MC syndrome Bloch-Sulzberger syndrome Chagas disease Klippel-Feil syndrome acquired immunodeficiency syndrome bacterial infectious disease bacterial sepsis blepharophimosis cleft lip cleft palate cleidocranial dysplasia congenital ptosis craniosynostosis cryptorchidism disseminated intravascular coagulation enterobiasis glomerulonephritis human immunodeficiency virus infectious disease humeroradial synostosis hypertropia hypomelanosis of Ito intellectual disability intestinal schistosomiasis isolated cleft palate kidney disease learning disability mechanical strabismus nephritis nephrosis neurodegenerative disease omphalocele ophthalmoplegia pneumonia ptosis purpura fulminans pyoureter radioulnar synostosis schistosomiasis scoliosis sensorineural hearing loss spina bifida occulta spondylolisthesis strabismus trichinosis trypanosomiasis tuberculosis umbilical hernia urinary schistosomiasis viral infectious disease
79701	2-oxoglutarate and iron dependent oxygenase domain containing 3	OGFOD3	Homo sapiens (human)
79748	lectin, mannose binding 1 like	LMAN1L Aliases: ERGIC-53L ERGL	Homo sapiens (human)
80201	hexokinase domain containing 1	HKDC1 Aliases: FLJ22761 FLJ37767	Homo sapiens (human)	breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer colorectal cancer colorectal carcinoma cone-rod dystrophy corneal disease embryoma fundus albipunctatus gestational diabetes glucose metabolism disease hepatitis hyperglycemia hyperinsulinemic hypoglycemia keratoconus large intestine cancer late-onset retinal degeneration lung benign neoplasm lung cancer lung carcinoma maturity-onset diabetes of the young retinitis pigmentosa steatotic liver disease
81035	collectin subfamily member 12	COLEC12 Aliases: CL-P1 SCARA4 SRCL	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis diabetes mellitus familial periodic paralysis multiple sclerosis myopathy substance abuse substance-related disorder type 2 diabetes mellitus

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