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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

Displaying entries **392476 - 392500** of **393515** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
17308	mannoside acetylglucosaminyltransferase 1	Mgat1	Mus musculus (house mouse)
17305	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	Mfng	Mus musculus (house mouse)
17254	solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2	Slc3a2	Mus musculus (house mouse)	adenoid cystic carcinoma lung adenocarcinoma lung non-small cell carcinoma lung pleomorphic carcinoma stomach carcinoma tongue squamous cell carcinoma transitional cell carcinoma
17193	methyl-CpG binding domain protein 4	Mbd4	Mus musculus (house mouse)	colorectal carcinoma esophagus squamous cell carcinoma lung cancer rheumatoid arthritis uveal melanoma
17160	mannosidase 2, alpha B2	Man2b2	Mus musculus (house mouse)
17159	mannosidase 2, alpha B1	Man2b1	Mus musculus (house mouse)	alpha-mannosidosis
17158	mannosidase 2, alpha 1	Man2a1	Mus musculus (house mouse)	congenital dyserythropoietic anemia systemic lupus erythematosus
17156	mannosidase, alpha, class 1A, member 2	Man1a2	Mus musculus (house mouse)
17155	mannosidase 1, alpha	Man1a	Mus musculus (house mouse)
17110	lysozyme 1	Lyz1	Mus musculus (house mouse)	familial visceral amyloidosis
17105	lysozyme 2	Lyz2	Mus musculus (house mouse)	familial visceral amyloidosis
17082	interleukin 1 receptor-like 1	Il1rl1	Mus musculus (house mouse)	Hantavirus hemorrhagic fever with renal syndrome Human papillomavirus infectious disease acute myocardial infarction asthma bacterial pneumonia chronic obstructive pulmonary disease coronary artery disease hemolytic-uremic syndrome idiopathic pulmonary fibrosis paracoccidioidomycosis rhinitis tongue squamous cell carcinoma
16973	low density lipoprotein receptor-related protein 5	Lrp5	Mus musculus (house mouse)	Worth syndrome autosomal dominant osteopetrosis 1 autosomal dominant polycystic kidney disease exudative vitreoretinopathy 4 exudative vitreoretinopathy heart valve disease idiopathic juvenile osteoporosis microphthalmia neovascular inflammatory vitreoretinopathy nonsyndromic deafness osteonecrosis osteoporosis-pseudoglioma syndrome osteoporosis polycystic liver disease tendinitis
16889	lysosomal acid lipase A	Lipa	Mus musculus (house mouse)	Wolman disease cholesterol ester storage disease lysosomal acid lipase deficiency
16848	LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	Lfng	Mus musculus (house mouse)	spondylocostal dysostosis 3
16847	leptin receptor	Lepr	Mus musculus (house mouse)	arteriosclerosis chronic kidney disease chronic obstructive pulmonary disease congestive heart failure coronary artery disease diastolic heart failure dilated cardiomyopathy glucose intolerance hepatocellular carcinoma hepatocellular clear cell carcinoma human immunodeficiency virus infectious disease hyperglycemia hyperinsulinism hypertension metabolic dysfunction-associated steatohepatitis metabolic dysfunction-associated steatotic liver disease obesity obstructive sleep apnea osteoporosis pancreatitis pre-eclampsia primary biliary cholangitis proteinuria renal fibrosis short bowel syndrome sleep apnea type 2 diabetes mellitus
16846	leptin	Lep	Mus musculus (house mouse)	Alzheimer's disease Huntington's disease Parkinson's disease abdominal obesity-metabolic syndrome 1 abdominal obesity-metabolic syndrome acute pancreatitis adult respiratory distress syndrome alcohol dependence alcoholic liver cirrhosis asthma breast cancer chronic obstructive pulmonary disease congenital leptin deficiency cystic fibrosis end stage renal disease familial hyperlipidemia gestational diabetes glucose intolerance hepatocellular carcinoma hepatocellular clear cell carcinoma hyperinsulinism hypertension hypogonadism lipid metabolism disorder lung non-small cell carcinoma metabolic dysfunction-associated steatotic liver disease obesity obstructive sleep apnea osteoarthritis osteoporosis pre-eclampsia primary biliary cholangitis renal cell carcinoma rhinitis short bowel syndrome steatotic liver disease type 2 diabetes mellitus
16828	lactate dehydrogenase A	Ldha	Mus musculus (house mouse)	disease of metabolism hyperglycemia hypertension
16795	LARGE xylosyl- and glucuronyltransferase 1	Large1	Mus musculus (house mouse)	congenital muscular dystrophy-dystroglycanopathy type A6 facioscapulohumeral muscular dystrophy muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B6
16770	lactalbumin, alpha	Lalba	Mus musculus (house mouse)	gastroenteritis
16592	fatty acid binding protein 5, epidermal	Fabp5	Mus musculus (house mouse)	prostate cancer psoriasis
16591	klotho	Kl	Mus musculus (house mouse)	chronic kidney disease coronary artery disease end stage renal disease familial hyperlipidemia hyperphosphatemic familial tumoral calcinosis hypertension intracranial embolism kidney disease kidney failure pulmonary emphysema retinitis pigmentosa secondary hyperparathyroidism spondylosis type 2 diabetes mellitus
16548	ketohexokinase	Khk	Mus musculus (house mouse)	essential fructosuria
16535	potassium voltage-gated channel, subfamily Q, member 1	Kcnq1	Mus musculus (house mouse)	Beckwith-Wiedemann syndrome Jervell-Lange Nielsen syndrome atrial fibrillation familial atrial fibrillation heart conduction disease hypertension long QT syndrome 1 long QT syndrome seminoma short QT syndrome type 2 diabetes mellitus
16514	potassium inwardly rectifying channel, subfamily J, member 11	Kcnj11	Mus musculus (house mouse)	Parkinsonism diabetes mellitus familial hyperinsulinemic hypoglycemia 2 hyperinsulinism hypertension maturity-onset diabetes of the young type 13 permanent neonatal diabetes mellitus prediabetes syndrome sciatic neuropathy status epilepticus type 2 diabetes mellitus visual epilepsy

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