GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **120576 - 120600** of **126547** in total

« First

‹ Prev

…

4820

4821

4822

4823

4824

4825

4826

4827

4828

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
Q9H3R5	Centromere protein H	CENPH ICEN35	Homo sapiens (human)	0	1
Q9R0G8	Nik-related protein kinase	Nrk Nesk	Mus musculus (house mouse)	2	1
Q99N94	Large ribosomal subunit protein bL9m	Mrpl9	Mus musculus (house mouse)	0	1
Q9NX65	Zinc finger and SCAN domain-containing protein 32	ZSCAN32 ZNF434	Homo sapiens (human)	0	1
P53094	Negative regulator of sporulation MDS3	MDS3	Saccharomyces cerevisiae S288C	17	1
P36086	Uncharacterized oxidoreductase YKL071W	YKL071W	Saccharomyces cerevisiae S288C	4	1
P78545	ETS-related transcription factor Elf-3	ELF3 ERT ESX JEN	Homo sapiens (human)	0	1
K2N002	Acyl-CoA dehydrogenase, mitochondrial, putative	MOQ_008310	Trypanosoma cruzi marinkellei	0	1
E9Q555	E3 ubiquitin-protein ligase RNF213	Rnf213 Mystr	Mus musculus (house mouse)	2	1
Q9HCY8	Protein S100-A14	S100A14 S100A15	Homo sapiens (human)	0	1
Q15046	Lysine--tRNA ligase	KARS1 KARS KIAA0070	Homo sapiens (human)	2	1
Q9ULD8	Potassium voltage-gated channel subfamily H member 3	KCNH3 KIAA1282	Homo sapiens (human)	4	1
P17098	Zinc finger protein 8	ZNF8	Homo sapiens (human)	0	1
Q6P2C8	Mediator of RNA polymerase II transcription subunit 27	MED27 CRSP34 CRSP8	Homo sapiens (human)	0	1
Q13415	Origin recognition complex subunit 1	ORC1 ORC1L PARC1	Homo sapiens (human)	0	1
Q9NRG9	Aladin	AAAS ADRACALA	Homo sapiens (human)	2	1
Q9Y2V7	Conserved oligomeric Golgi complex subunit 6	COG6 KIAA1134	Homo sapiens (human)	2	1	Gilbert syndrome acquired hyperkeratosis allergic asthma anemia anhidrosis asthma bilirubin metabolic disorder blood coagulation disease cerebral degeneration cholestasis congenital disorder of glycosylation type II congenital disorder of glycosylation type IIl congenital disorder of glycosylation coronary artery disease dental caries dental enamel hypoplasia dentin caries developmental and epileptic encephalopathy 36 epilepsy gastroenteritis gastrointestinal system disease hydrocephalus hypohidrosis intellectual disability intestinal disease intrinsic asthma juvenile rheumatoid arthritis learning disability leiomyoma macrocytic anemia microcephaly myofibroma nonepidermolytic palmoplantar keratoderma palmoplantar keratosis pancytopenia parapsoriasis placental insufficiency primary biliary cholangitis primary immunodeficiency disease proctitis psoriasis pustulosis of palm and sole rheumatoid arthritis systemic lupus erythematosus thrombocytopenia uterine fibroid visual epilepsy
F1LSC3	Splicing factor 1	Sf1	Rattus norvegicus (Norway rat)	0	1
Q14151	Scaffold attachment factor B2	SAFB2 KIAA0138	Homo sapiens (human)	1	1
O95391	Pre-mRNA-splicing factor SLU7	SLU7	Homo sapiens (human)	1	1
A0A494B9W3	Fermitin family member 3	Fermt3	Mus musculus (house mouse)	0	1
D3YX99	NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 5, mitochondrial (Fragment)	Ndufb5	Mus musculus (house mouse)	0	1
P98198	Phospholipid-transporting ATPase ID	ATP8B2 ATPID KIAA1137	Homo sapiens (human)	3	1
Q8BGD6	Neutral amino acid transporter 9	Slc38a9	Mus musculus (house mouse)	4	1
V5BNW7	Flagellar Member 5	TCDM_03354	Trypanosoma cruzi Dm28c	0	1

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements