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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 "hydrolase activity, acting on glycosyl bonds"

Displaying entries **201 - 225** of **16787** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
50877	neuraminidase 3	Neu3	Mus musculus (house mouse)
51172	N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase	NAGPA Aliases: APAA UCE	Homo sapiens (human)	Fabry disease alexia chylomicron retention disease dyslexia glycoproteinosis lipid storage disease mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucopolysaccharidosis III mucopolysaccharidosis type IIIB neurodegenerative disease stuttering
54447	N-acylsphingosine amidohydrolase 2	Asah2	Mus musculus (house mouse)	cardiomyopathy
54936	ADP-ribosylserine hydrolase	ADPRS Aliases: ADP-ribosylarginine hydrolase like 2 ARH3 FLJ20446	Homo sapiens (human)	autosomal recessive hypercholesterolemia brain stem infarction breast cancer breast carcinoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease congenital nystagmus congenital ptosis dissociated nystagmus epilepsy hypertropia intellectual disability learning disability mechanical strabismus neurodegenerative disease ophthalmoplegia pathologic nystagmus ptosis spontaneous ocular nystagmus strabismus stress-induced childhood-onset neurodegeneration with variable ataxia and seizures visual epilepsy
55247	nei like DNA glycosylase 3	NEIL3 Aliases: FLJ10858 FPG2 ZGRF3 hFPG2 hNEI3 zinc finger, GRF-type containing 3	Homo sapiens (human)	Fanconi anemia acute myocardial infarction basal cell carcinoma cancer coronary thrombosis differentiated thyroid gland carcinoma embryoma giant cell glioblastoma glioblastoma glomerulonephritis hepatocellular carcinoma kidney disease liver cancer myocardial infarction nephritis silent myocardial infarction
55331	alkaline ceramidase 3	ACER3 Aliases: APHC FLJ11238 alkaline phytoceramidase	Homo sapiens (human)	Cauda equina syndrome Laron syndrome achondroplasia acute myeloid leukemia cerebellar ataxia cerebellar disease cerebral degeneration dystonia hepatocellular carcinoma intellectual disability learning disability leukodystrophy liver cancer melanoma metabolic dysfunction-associated steatohepatitis neurogenic bladder neuropathy peripheral nervous system disease skin melanoma
55347	abhydrolase domain containing 10, depalmitoylase	ABHD10 Aliases: FLJ11342 Mycophenolic acid acyl-glucuronide esterase, mitochondrial	Homo sapiens (human)
55741	ER degradation enhancing alpha-mannosidase like protein 2	EDEM2 Aliases: FLJ10783 bA4204.1	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Pick's disease Reye syndrome cerebral degeneration leiomyoma myofibroma schizophrenia uterine fibroid
57134	mannosidase alpha class 1C member 1	MAN1C1 Aliases: HMIC	Homo sapiens (human)	cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma nonpapillary renal cell carcinoma papillary renal cell carcinoma pulmonary emphysema renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia
57151	lysozyme like 6	LYZL6 Aliases: LYC1 PRO1485 TKAL754	Homo sapiens (human)
57214	cell migration inducing hyaluronidase 1	CEMIP Aliases: HYBID IR2155535 TMEM2L hyaluronan-binding protein involved in hyaluronan depolymerization	Homo sapiens (human)	acute myeloid leukemia adenocarcinoma adenoma arthritis arthropathy breast cancer breast carcinoma cancer chromophobe renal cell carcinoma chronic fatigue syndrome clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart cribriform carcinoma embryoma encephalitis encephalomyelitis familial adenomatous polyposis 2 familial retinoblastoma follicular adenoma granular cell carcinoma hepatocellular carcinoma idiopathic interstitial pneumonia idiopathic pulmonary fibrosis large intestine cancer liver cancer lung cancer lung non-small cell carcinoma microcystic adenoma microphthalmia multiple sclerosis myelitis nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome osteoarthritis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma pneumonia prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma retinoblastoma rheumatoid arthritis sarcomatoid renal cell carcinoma stomach cancer stomach carcinoma thyroid gland papillary carcinoma trilateral retinoblastoma tubular adenocarcinoma
57377	mannosyl-oligosaccharide glucosidase	Mogs	Mus musculus (house mouse)	congenital disorder of glycosylation type IIb
57462	myogenesis regulating glycosidase (putative)	MYORG Aliases: NET37	Homo sapiens (human)	amnestic disorder basal ganglia calcification choreatic disease dystonia epilepsy hydrocephalus lingual-facial-buccal dyskinesia microcephaly migraine neurodegenerative disease placental insufficiency recurrent corneal erosion retrograde amnesia secondary Parkinson disease syndromic X-linked intellectual disability type 10 thrombocytopenia visual epilepsy
57704	glucosylceramidase beta 2	GBA2 Aliases: AD035 DKFZp762K054 KIAA1605 bile acid beta-glucosidase glucocerebrosidase 2 non-lysosomal glucosylceramidase	Homo sapiens (human)	Charcot-Marie-Tooth disease type 5 Gaucher's disease Henoch-Schoenlein purpura Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease MASA syndrome Mast syndrome Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease SPOAN syndrome Troyer syndrome alternating hemiplegia of childhood autonomic neuropathy cancer cataract central nervous system disease cerebellar ataxia cerebellar disease cerebral degeneration congenital nystagmus cystic fibrosis dementia dissociated nystagmus glaucoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia hypersensitivity vasculitis infertility intellectual disability learning disability male infertility nervous system disease paraplegia pathologic nystagmus scoliosis sensorineural hearing loss spontaneous ocular nystagmus trichohepatoenteric syndrome 1 trichohepatoenteric syndrome
57733	glucosylceramidase beta 3 (gene/pseudogene)	GBA3 Aliases: CBGL1 GLUC KLrP cytosolic β-glucosidase-like protein-1 klotho-related protein	Homo sapiens (human)	Gaucher's disease type I Gaucher's disease Goodpasture syndrome Takayasu's arteritis West Nile fever allergic asthma asthma cancer cystic fibrosis diabetic ketoacidosis granulomatosis with polyangiitis hepatocellular carcinoma kidney disease liver cancer obsolete type 1 diabetes mellitus 9 polyarteritis nodosa stomach cancer stomach carcinoma substance abuse substance-related disorder type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus
58866	trehalase (brush-border membrane glycoprotein)	Treh	Mus musculus (house mouse)
60367	interleukin 1 receptor accessory protein-like 2	Il1rapl2	Mus musculus (house mouse)
60495	heparanase 2 (inactive)	HPSE2 Aliases: HPA2 HPR2	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Bloom syndrome Down syndrome Evans' syndrome Glanzmann's thrombasthenia Japanese encephalitis Pick's disease Reye syndrome Richter's syndrome T-cell acute lymphoblastic leukemia acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma allergic asthma arteriosclerotic cardiovascular disease asthma atherosclerosis autoimmune thrombocytopenic purpura bladder carcinoma breast cancer cancer cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma chronic lymphocytic leukemia coronary artery disease coronary thrombosis cribriform carcinoma cryptorchidism dengue disease diabetic ketoacidosis dyskeratosis congenita essential hypertension essential thrombocythemia factor VIII deficiency gestational diabetes gestational trophoblastic neoplasm glaucoma granular cell carcinoma gray platelet syndrome head and neck squamous cell carcinoma hepatitis B hepatitis C hydronephrosis hypertension kidney failure kwashiorkor leiomyoma marasmus migraine multiple myeloma myelodysplastic syndrome myocardial infarction myofibroma nutmeg liver nutrition disease obsolete constipation obsolete type 1 diabetes mellitus 9 ocular hypertension platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 prostate cancer prostate carcinoma protein-energy malnutrition proteinuria qualitative platelet defect silent myocardial infarction squamous cell carcinoma tongue squamous cell carcinoma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tubular adenocarcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus urethral obstruction urinary bladder cancer urinary tract obstruction urofacial syndrome uterine fibroid vesicoureteral reflux viral infectious disease yellow fever
64537	heparanase	Hpse	Rattus norvegicus (Norway rat)
64772	endo-beta-N-acetylglucosaminidase	ENGASE Aliases: Di-N-acetylchitobiosyl beta-N-acetylglucosaminidase FLJ21865 Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase	Homo sapiens (human)	NGLY1-deficiency breast cancer breast carcinoma rheumatoid arthritis
66190	alkaline ceramidase 3	Acer3	Mus musculus (house mouse)	hepatocellular carcinoma leukodystrophy metabolic dysfunction-associated steatohepatitis
66848	fucosidase, alpha-L- 2, plasma	Fuca2	Mus musculus (house mouse)
66967	ER degradation enhancer, mannosidase alpha-like 3	Edem3	Mus musculus (house mouse)	congenital disorder of glycosylation type II
67328	lysozyme-like 1	Lyzl1	Mus musculus (house mouse)
69032	lysozyme-like 4	Lyzl4	Mus musculus (house mouse)

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