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 **7851 - 7875** of **9988** in total

« First

‹ Prev

…

311

312

313

314

315

316

317

318

319

…

Next ›

Last »
Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
1798	dolichyl-phosphate N-acetylglucosaminephosphotransferase 1	DPAGT1 Aliases: ALG7 CDG-Ij D11S366 DGPT GPT GlcNAc-1-P transferase 1 UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase 1	Homo sapiens (human)	Bell's palsy Ebola hemorrhagic fever Lambert-Eaton myasthenic syndrome acute intermittent porphyria agnosia alternating exotropia breast cancer cancer cataract clubfoot colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ij congenital disorder of glycosylation type I congenital disorder of glycosylation congenital myasthenic syndrome 13 congenital myasthenic syndrome congenital nystagmus congenital ptosis cutaneous leishmaniasis developmental and epileptic encephalopathy 36 developmental coordination disorder dissociated nystagmus epilepsy essential hypertension exotropia facial nerve disease facial paralysis familial periodic paralysis fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome glycoproteinosis hepatocellular carcinoma hypertension intellectual disability isolated elevated serum creatine phosphokinase levels large intestine cancer learning disability leishmaniasis liver cancer microcephaly monocular exotropia mucolipidosis II alpha/beta myopathy pathologic nystagmus pseudosarcomatous fibromatosis ptosis scoliosis spontaneous ocular nystagmus squamous cell carcinoma stomach cancer stomach carcinoma stuttering syndromic X-linked intellectual disability 94 tongue squamous cell carcinoma tuberculosis visceral leishmaniasis visual epilepsy
8641	protocadherin gamma subfamily B, 4	PCDHGB4	Homo sapiens (human)
57513	CASK interacting protein 2	CASKIN2	Homo sapiens (human)
11315	Parkinsonism associated deglycase	PARK7	Homo sapiens (human)
54906	transcription activation suppressor family member 2	TASOR2	Homo sapiens (human)
80031	semaphorin 6D	SEMA6D	Homo sapiens (human)
701	BUB1 mitotic checkpoint serine/threonine kinase B	BUB1B	Homo sapiens (human)
90673	protein phosphatase 1 regulatory subunit 3E	PPP1R3E	Homo sapiens (human)
284358	MEF2 activating motif and SAP domain containing transcriptional regulator	MAMSTR	Homo sapiens (human)
100188893	translocase of outer mitochondrial membrane 6	TOMM6	Homo sapiens (human)
117289	T cell activation RhoGTPase activating protein	TAGAP	Homo sapiens (human)
9500	MAGE family member D1	MAGED1	Homo sapiens (human)
309	annexin A6	ANXA6	Homo sapiens (human)
2570	gamma-aminobutyric acid type A receptor subunit rho2	GABRR2	Homo sapiens (human)
51092	SID1 transmembrane family member 2	SIDT2	Homo sapiens (human)
128408	basic helix-loop-helix family member e23	BHLHE23	Homo sapiens (human)
7360	UDP-glucose pyrophosphorylase 2	UGP2 Aliases: SVUGP2 UGPP1 UTP--glucose-1-phosphate uridylyltransferase	Homo sapiens (human)	cancer central nervous system cancer classic galactosemia cystinuria developmental and epileptic encephalopathy 83 galactokinase deficiency galactosemia giant cell glioblastoma glioblastoma gliosarcoma glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hepatocellular carcinoma high grade glioma liver cancer lung cancer lung non-small cell carcinoma mixed glioma pancreatic cancer pancreatic carcinoma pancreatic ductal carcinoma paroxysmal nonkinesigenic dyskinesia 1
8778	sialic acid binding Ig like lectin 5	SIGLEC5 Aliases: CD170 OB-BP2 SIGLEC-5	Homo sapiens (human)	acute myeloid leukemia acute pericementitis aggressive periodontitis cancer diabetes mellitus diabetic ketoacidosis leprosy periodontitis periodontosis systemic lupus erythematosus type 2 diabetes mellitus
129401	nucleoporin 35	NUP35	Homo sapiens (human)
219931	two pore segment channel 2	TPCN2	Homo sapiens (human)
9733	spliceosome associated factor 3, U4/U6 recycling protein	SART3	Homo sapiens (human)
11177	bromodomain adjacent to zinc finger domain 1A	BAZ1A	Homo sapiens (human)
201780	solute carrier family 10 member 4	SLC10A4	Homo sapiens (human)
55005	required for meiotic nuclear division 1 homolog	RMND1	Homo sapiens (human)
79595	Sin3A associated protein 130	SAP130	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