GlyCosmos Portal

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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 **9826 - 9850** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▼	Disease Ontology
339287	MSL complex subunit 1	MSL1	Homo sapiens (human)
4669	N-acetyl-alpha-glucosaminidase	NAGLU Aliases: NAG Sanfilippo disease IIIB	Homo sapiens (human)	Alzheimer's disease Burkitt lymphoma Charcot-Marie-Tooth disease axonal type 2V Clouston syndrome Dent disease Fanconi syndrome Glanzmann's thrombasthenia Kluver-Bucy syndrome Legg-Calve-Perthes disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma amnestic disorder amyloidosis appendicitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrophic gastritis autistic disorder cancer cardiovascular system disease cholera chronic kidney disease chronic pyelonephritis cone-rod dystrophy congestive heart failure coronary artery disease cribriform carcinoma cystinosis cystitis dementia dentatorubral-pallidoluysian atrophy diabetes mellitus diabetic ketoacidosis diarrhea embryoma epilepsy essential thrombocythemia focal segmental glomerulosclerosis follicular adenoma fundus albipunctatus glomerulonephritis granular cell carcinoma gray platelet syndrome heart disease hydronephrosis hypertrichosis hypertrophic cardiomyopathy 1 intellectual disability kidney disease kidney failure learning disability lipoid nephrosis liver cirrhosis lysosomal storage disease malignant pleural mesothelioma microcystic adenoma mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IIIC mucopolysaccharidosis type IIID mucopolysaccharidosis multiple epiphyseal dysplasia multiple myeloma myelodysplastic syndrome nephritis nephrosis neuroblastoma neurodegenerative disease oculocerebrorenal syndrome oculocutaneous albinism type IA osteochondrodysplasia otitis media panic disorder papillary adenoma parapsoriasis platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 progressive familial intrahepatic cholestasis 1 progressive myoclonus epilepsy prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole pyoureter qualitative platelet defect renal osteodystrophy retinitis pigmentosa retrograde amnesia sensorineural hearing loss spondyloepimetaphyseal dysplasia, Sponastrime type stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 trigonitis tubular adenocarcinoma type 2 diabetes mellitus viral infectious disease visual epilepsy
9400	RecQ like helicase 5	RECQL5	Homo sapiens (human)
338328	glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1	GPIHBP1 Aliases: GPI-HBP1 LOC338328 endothelial cell LPL transporter	Homo sapiens (human)	acute pancreatitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cardiovascular system disease central nervous system cancer chylomicron retention disease colitis coronary artery disease diabetes mellitus diabetic ketoacidosis disease of metabolism familial GPIHBP1 deficiency familial hyperlipidemia familial lipoprotein lipase deficiency gastroenteritis gliosarcoma heart disease high grade glioma hyperlipoproteinemia type V ileitis ileocolitis mixed glioma nutmeg liver obesity pancreatitis type 2 diabetes mellitus
23627	prion like protein doppel	PRND	Homo sapiens (human)
128954	GRB2 associated binding protein family member 4	GAB4	Homo sapiens (human)
343066	arylacetamide deacetylase like 4	AADACL4 Aliases: OTTHUMG00000001889	Homo sapiens (human)
148113	cartilage intermediate layer protein 2	CILP2	Homo sapiens (human)
138311	divergent protein kinase domain 1B	DIPK1B	Homo sapiens (human)
8038	ADAM metallopeptidase domain 12	ADAM12	Homo sapiens (human)
5004	orosomucoid 1	ORM1	Homo sapiens (human)
54910	semaphorin 4C	SEMA4C	Homo sapiens (human)
56141	protocadherin alpha 7	PCDHA7	Homo sapiens (human)
158358	bromodomain containing 10	BRD10	Homo sapiens (human)
29121	C-type lectin domain family 2 member D	CLEC2D	Homo sapiens (human)
10942	serine protease 21	PRSS21 Aliases: ESP-1 TEST1 testisin	Homo sapiens (human)	Behcet's disease Down syndrome acquired immunodeficiency syndrome alcohol dependence alcohol use disorder atrial fibrillation cancer cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood germ cell cancer diabetes mellitus diabetic ketoacidosis disorder of sexual development embryonal cancer germ cell and embryonal cancer germ cell cancer germinoma hepatitis B hermaphroditism human immunodeficiency virus infectious disease monoclonal gammopathy of uncertain significance monoclonal paraproteinemia ovarian cancer ovarian carcinoma plasma cell neoplasm pseudohermaphroditism type 2 diabetes mellitus
11012	kallikrein related peptidase 11	KLK11	Homo sapiens (human)
6167	ribosomal protein L37	RPL37	Homo sapiens (human)
146705	TEPSIN adaptor related protein complex 4 accessory protein	TEPSIN	Homo sapiens (human)
7534	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta	YWHAZ	Homo sapiens (human)
84674	caspase recruitment domain family member 6	CARD6	Homo sapiens (human)
283537	solute carrier family 46 member 3	SLC46A3	Homo sapiens (human)
27068	inorganic pyrophosphatase 2	PPA2 Aliases: FLJ20459	Homo sapiens (human)
57292	killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 5A	KIR2DL5A	Homo sapiens (human)
10592	structural maintenance of chromosomes 2	SMC2	Homo sapiens (human)

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