GlyCosmos Portal

Table Filtering

Gene ID

Gene Name

Gene Symbol

Organism

Taxonomy ID

Disease Ontology

Disease Ontology ID

Gene Ontology

Gene Ontology ID

Display
results per page.

Clear

Submissions

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 **418501 - 418525** of **422592** in total

« First

‹ Prev

…

16737

16738

16739

16740

16741

16742

16743

16744

16745

…

Next ›

Last »
Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
9685	clathrin interactor 1	CLINT1	Homo sapiens (human)
9684	leucine rich repeat containing 14	LRRC14	Homo sapiens (human)
9683	NEDD4 binding protein 1	N4BP1	Homo sapiens (human)
9681	DEP domain containing 5, GATOR1 subcomplex subunit	DEPDC5	Homo sapiens (human)
9679	family with sequence similarity 53 member B	FAM53B	Homo sapiens (human)
9678	PHD finger protein 14	PHF14	Homo sapiens (human)
9675	TELO2 interacting protein 1	TTI1	Homo sapiens (human)
9672	syndecan 3	SDC3 Aliases: N-syndecan SYND3 syndecan proteoglycan 3	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 Creutzfeldt-Jakob disease Duchenne muscular dystrophy Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 breast fibrocystic disease cancer cerebral degeneration chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma embryoma hepatitis C hepatocellular carcinoma liver cancer microglandular adenosis muscular dystrophy nonpapillary renal cell carcinoma obesity pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid renal cell carcinoma
9671	WSC domain containing 2	WSCD2	Homo sapiens (human)
9669	eukaryotic translation initiation factor 5B	EIF5B Aliases: DKFZp434I036 FLJ10524 IF2 KIAA0741 translation initiation factor IF2	Homo sapiens (human)
9668	zinc finger protein 432	ZNF432	Homo sapiens (human)
9667	scaffold attachment factor B2	SAFB2	Homo sapiens (human)
9665	meiosis regulator and mRNA stability factor 1	MARF1	Homo sapiens (human)
9663	lipin 2	LPIN2 Aliases: KIAA0249	Homo sapiens (human)	Chanarin-Dorfman syndrome Crohn's colitis Crohn's disease Diamond-Blackfan anemia SAPHO syndrome acne agranulocytosis allergic asthma anemia asthma autosomal recessive congenital ichthyosis 1 autosomal recessive osteopetrosis 7 cancer chronic recurrent multifocal osteomyelitis congenital dyserythropoietic anemia congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital hypoplastic anemia congestive heart failure dermatitis diabetes mellitus diabetic ketoacidosis disease of metabolism familial mediterranean fever familial periodic paralysis fibromyalgia gastrointestinal system disease glomerulonephritis granular corneal dystrophy 2 ichthyosis inflammatory bowel disease 1 inflammatory bowel disease intestinal disease intrinsic asthma keratosis follicularis leukopenia lipid metabolism disorder lipoatrophic diabetes mellitus lipodystrophy macrocytic anemia mevalonic aciduria microcytic anemia mongolian spot myoglobinuria myopathy myopia myositis nephritis neutropenia obesity obsolete congenital ichthyosiform erythroderma osteomyelitis osteopetrosis osteosclerosis prostate cancer prostate carcinoma proteinuria pseudoxanthoma elasticum relapsing fever rheumatoid arthritis severe congenital neutropenia synovitis tenosynovitis trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tropical sprue type 2 diabetes mellitus ulcerative colitis
9662	centrosomal protein 135	CEP135	Homo sapiens (human)
9659	phosphodiesterase 4D interacting protein	PDE4DIP	Homo sapiens (human)
9658	zinc finger protein 516	ZNF516	Homo sapiens (human)
9656	mediator of DNA damage checkpoint 1	MDC1	Homo sapiens (human)
9654	tubulin tyrosine ligase like 4	TTLL4	Homo sapiens (human)
9653	heparan sulfate 2-O-sulfotransferase 1	HS2ST1 Aliases: KIAA0448	Homo sapiens (human)	benign mastocytoma extracutaneous mastocytoma hypereosinophilic syndrome indolent systemic mastocytosis mast cell neoplasm mastocytosis melanoma skin melanoma
9652	SKI3 subunit of superkiller complex	SKIC3	Homo sapiens (human)
9651	phospholipase C eta 2	PLCH2 Aliases: 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-2 KIAA0450 PLC-eta2 PLCeta2 RP3-395M20.1	Homo sapiens (human)	azoospermia intellectual disability learning disability schizophrenia
9650	mitochondrial fission regulator 1	MTFR1	Homo sapiens (human)
9649	Ral GEF with PH domain and SH3 binding motif 1	RALGPS1	Homo sapiens (human)
9648	GRIP and coiled-coil domain containing 2	GCC2	Homo sapiens (human)

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements