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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 **6501 - 6525** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▼	Disease Ontology
2030	solute carrier family 29 member 1 (Augustine blood group)	SLC29A1	Homo sapiens (human)
9521	eukaryotic translation elongation factor 1 epsilon 1	EEF1E1	Homo sapiens (human)
255057	CACN subunit beta associated regulatory protein	CBARP	Homo sapiens (human)
9774	BCL2 associated transcription factor 1	BCLAF1	Homo sapiens (human)
23077	MYC binding protein 2	MYCBP2	Homo sapiens (human)
1281	collagen type III alpha 1 chain	COL3A1	Homo sapiens (human)
2650	glucosaminyl (N-acetyl) transferase 1	GCNT1 Aliases: C2GNT NAGCT2 beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N--acetylglucosaminyltransferase core 2 beta1,6 N-acetylglucosaminyltransferase-I	Homo sapiens (human)	adenocarcinoma adenoma bronchus cancer bronchus carcinoma cancer carcinoma colorectal cancer colorectal carcinoma cribriform carcinoma embryoma granular cell carcinoma large intestine cancer lung benign neoplasm lung cancer lung carcinoma neuroblastoma pancreatic cancer pancreatic carcinoma prostate cancer prostate carcinoma sarcomatoid carcinoma seminoma testicular cancer testicular germ cell cancer tubular adenocarcinoma
9568	gamma-aminobutyric acid type B receptor subunit 2	GABBR2	Homo sapiens (human)
9563	hexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase	H6PD Aliases: 6-phosphogluconolactonase GDH/6PGL endoplasmic bifunctional protein H6PDH	Homo sapiens (human)	Alzheimer's disease B-cell lymphoma Laron syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acne aromatase excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis beta thalassemia breast cancer breast carcinoma cancer cardiovascular system disease cholangiocarcinoma colorectal cancer cone-rod dystrophy 2 cone-rod dystrophy coronary artery disease cortisone reductase deficiency 1 cortisone reductase deficiency dementia diabetes insipidus diabetes mellitus diabetic ketoacidosis diarrhea gallbladder disease giardiasis heart disease hemolytic anemia hyperandrogenism hyperinsulinism hypertrichosis hypoglycemia infertility intrahepatic cholangiocarcinoma large intestine cancer leishmaniasis liver disease luminal breast carcinoma A malaria multiple sclerosis neurohypophyseal diabetes insipidus obesity obsolete ymphosarcoma placental insufficiency polycystic ovary syndrome primary hyperoxaluria steatotic liver disease thalassemia type 2 diabetes mellitus visceral leishmaniasis
27177	interleukin 36 beta	IL36B	Homo sapiens (human)
56928	signal peptide peptidase like 2B	SPPL2B	Homo sapiens (human)
58477	SRP receptor subunit beta	SRPRB	Homo sapiens (human)
59338	pleckstrin homology domain containing A1	PLEKHA1	Homo sapiens (human)
7205	thyroid hormone receptor interactor 6	TRIP6	Homo sapiens (human)
199731	cell adhesion molecule 4	CADM4	Homo sapiens (human)
55690	phosphofurin acidic cluster sorting protein 1	PACS1	Homo sapiens (human)
389118	cadherin related family member 4	CDHR4	Homo sapiens (human)
2237	flap structure-specific endonuclease 1	FEN1	Homo sapiens (human)
7415	valosin containing protein	VCP Aliases: CDC48 IBMPFD TERA p97 transitional endoplasmic reticulum ATPase	Homo sapiens (human)
347527	arylsulfatase family member H	ARSH	Homo sapiens (human)	Marfan syndrome Richter's syndrome X-linked chondrodysplasia punctata 1 acquired immunodeficiency syndrome acrodermatitis alcoholic liver cirrhosis autosomal dominant chondrodysplasia punctata cancer childhood leukemia chondrodysplasia punctata chronic lymphocytic leukemia dermatitis dyschromatosis symmetrica hereditaria essential thrombocythemia gallbladder disease hepatitis human immunodeficiency virus infectious disease leukemia liver cirrhosis liver disease microphthalmia mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis mucosulfatidosis myelodysplastic syndrome neuroblastoma obsolete Matthew-Wood syndrome oculocerebrorenal syndrome rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 situs inversus tuberous sclerosis ventricular septal defect
138716	ribonuclease P/MRP subunit p25 like	RPP25L	Homo sapiens (human)
1139	cholinergic receptor nicotinic alpha 7 subunit	CHRNA7	Homo sapiens (human)
10492	synaptotagmin binding cytoplasmic RNA interacting protein	SYNCRIP	Homo sapiens (human)
79867	tectonic family member 2	TCTN2	Homo sapiens (human)
29106	secretogranin III	SCG3	Homo sapiens (human)

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