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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	July 8, 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 **76 - 100** of **3909** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
64035	glycogen phosphorylase L	Pygl	Rattus norvegicus (Norway rat)	glycogen storage disease VI glycogen storage disease lactic acidosis
65152	phosphofructokinase, muscle	Pfkm	Rattus norvegicus (Norway rat)	disease of metabolism glycogen storage disease VII glycogen storage disease
66171	6-phosphogluconolactonase	Pgls	Mus musculus (house mouse)
66646	ribulose-5-phosphate-3-epimerase	Rpe	Mus musculus (house mouse)
69064	fucose mutarotase	Fuom	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
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
81562	lectin, mannose binding 2 like	LMAN2L Aliases: DKFZp564L2423 VIP36-like VIPL	Homo sapiens (human)	agnosia attention deficit hyperactivity disorder autosomal dominant intellectual developmental disorder autosomal recessive intellectual developmental disorder 52 bipolar disorder borderline personality disorder cerebral degeneration choreatic disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma depressive disorder developmental coordination disorder dysthymic disorder dystonia epilepsy focal epilepsy intermittent explosive disorder lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder nonpapillary renal cell carcinoma obsolete infantile epileptic encephalopathy obsolete melancholia papillary adenocarcinoma papillary renal cell carcinoma partial motor epilepsy pulmonary emphysema renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 thyroid gland papillary carcinoma visual epilepsy
81675	glycogenin 1	Gyg1	Rattus norvegicus (Norway rat)	glycogen storage disease XV glycogen storage disease
83688	transaldolase 1	Taldo1	Rattus norvegicus (Norway rat)	carbohydrate metabolic disorder
93978	C-type lectin domain containing 6A	CLEC6A Aliases: dectin-2 hDECTIN-2	Homo sapiens (human)	Kawasaki disease acute myocardial infarction arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer candidiasis cholesteatoma coronary artery disease coronary thrombosis cryptococcosis cystic fibrosis dermatomycosis dermatophytosis embryoma fungal infectious disease myocardial infarction pneumocystosis pneumonia polyp of middle ear rheumatoid arthritis silent myocardial infarction superficial mycosis tinea favosa tuberculosis vasculitis
103988	glucokinase	Gck	Mus musculus (house mouse)	coronary artery disease diabetes mellitus familial hyperinsulinemic hypoglycemia 3 gestational diabetes glucose metabolism disease hyperglycemia hyperinsulinemic hypoglycemia hyperinsulinism hypertension hypoglycemia maturity-onset diabetes of the young type 2 maturity-onset diabetes of the young obesity permanent neonatal diabetes mellitus steatotic liver disease type 2 diabetes mellitus
110095	liver glycogen phosphorylase	Pygl	Mus musculus (house mouse)	glycogen storage disease VI glycogen storage disease lactic acidosis
110173	mannosidase, beta A, lysosomal	Manba	Mus musculus (house mouse)	beta-mannosidosis
117364	Hexokinase testis 1	Hex-t1	Drosophila melanogaster (fruit fly)	coronary artery disease diabetes mellitus familial hyperinsulinemic hypoglycemia 3 gestational diabetes hyperglycemia hyperinsulinemic hypoglycemia hyperinsulinism hypertension hypoglycemia maturity-onset diabetes of the young type 2 maturity-onset diabetes of the young obesity permanent neonatal diabetes mellitus retinitis pigmentosa steatotic liver disease type 2 diabetes mellitus
179335	ATP-dependent 6-phosphofructokinase 2	pfk-1.2	Caenorhabditis elegans	disease of metabolism glycogen storage disease VII glycogen storage disease
180583	ATP-dependent 6-phosphofructokinase 1	pfk-1.1	Caenorhabditis elegans	disease of metabolism glycogen storage disease VII glycogen storage disease
211286	ceroid-lipofuscinosis, neuronal 5	Cln5	Mus musculus (house mouse)	neuronal ceroid lipofuscinosis 5
212032	hexokinase 3	Hk3	Mus musculus (house mouse)	glucose metabolism disease
216019	hexokinase domain containing 1	Hkdc1	Mus musculus (house mouse)	glucose metabolism disease retinitis pigmentosa
216558	UDP-glucose pyrophosphorylase 2	Ugp2	Mus musculus (house mouse)	cancer developmental and epileptic encephalopathy 83
230163	aldolase B, fructose-bisphosphate	Aldob	Mus musculus (house mouse)	hereditary fructose intolerance syndrome liver benign neoplasm peritonitis type 2 diabetes mellitus
232493	glycogen synthase 2	Gys2	Mus musculus (house mouse)	Lafora disease glycogen storage disease

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