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 **118726 - 118750** of **126547** in total

« First

‹ Prev

…

4746

4747

4748

4749

4750

4751

4752

4753

4754

…

Next ›

Last »
UniProt ID ▲	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9P2G9	Kelch-like protein 8	KLHL8 KIAA1378	Homo sapiens (human)	0	1
Q9P2H0	Centrosomal protein of 126 kDa	CEP126 KIAA1377	Homo sapiens (human)	0	1
Q9P2H5	Ubiquitin carboxyl-terminal hydrolase 35	USP35 KIAA1372 USP34	Homo sapiens (human)	1	1
Q9P2I0	Cleavage and polyadenylation specificity factor subunit 2	CPSF2 CPSF100 KIAA1367	Homo sapiens (human)	1	1
Q9P2J2	Protein turtle homolog A	IGSF9 IGSF9A KIAA1355 NRT1	Homo sapiens (human)	5	6
Q9P2J3	Kelch-like protein 9	KLHL9 KIAA1354	Homo sapiens (human)	1	1
Q9P2J5	Leucine--tRNA ligase, cytoplasmic	LARS1 KIAA1352 LARS	Homo sapiens (human)	7	1
Q9P2K1	Coiled-coil and C2 domain-containing protein 2A	CC2D2A KIAA1345	Homo sapiens (human)	2	1
Q9P2K2	Thioredoxin domain-containing protein 16	TXNDC16 ERP90 KIAA1344	Homo sapiens (human)	1	3
Q9P2K5	Myelin expression factor 2	MYEF2 KIAA1341	Homo sapiens (human)	0	1
Q9P2K6	Kelch-like protein 42	KLHL42 KIAA1340 KLHDC5	Homo sapiens (human)	1	1
Q9P2K9	Protein dispatched homolog 3	DISP3 KIAA1337 PTCHD2	Homo sapiens (human)	2	2
Q9P2L0	WD repeat-containing protein 35	WDR35 IFT121 KIAA1336	Homo sapiens (human)	1	2
Q9P2M4	TBC1 domain family member 14	TBC1D14 KIAA1322	Homo sapiens (human)	0	1
Q9P2N2	Rho GTPase-activating protein 28	ARHGAP28 KIAA1314	Homo sapiens (human)	1	2
Q9P2N4	A disintegrin and metalloproteinase with thrombospondin motifs 9	ADAMTS9 KIAA1312	Homo sapiens (human)	11	5
Q9P2N5	RNA-binding protein 27	RBM27 KIAA1311	Homo sapiens (human)	21	2
Q9P2N6	KAT8 regulatory NSL complex subunit 3	KANSL3 KIAA1310 NSL3 PRTD SI1	Homo sapiens (human)	29	1
Q9P2P1	Protein NYNRIN	NYNRIN CGIN1 KIAA1305	Homo sapiens (human)	1	1
Q9P2P5	E3 ubiquitin-protein ligase HECW2	HECW2 KIAA1301 NEDL2	Homo sapiens (human)	0	1
Q9P2P6	StAR-related lipid transfer protein 9	STARD9 KIAA1300	Homo sapiens (human)	3	2
Q9P2R3	Rabankyrin-5	ANKFY1 ANKHZN KIAA1255	Homo sapiens (human)	1	2
Q9P2R6	Arginine-glutamic acid dipeptide repeats protein	RERE ARG ARP ATN1L KIAA0458	Homo sapiens (human)	7	2
Q9P2R7	Succinate--CoA ligase [ADP-forming] subunit beta, mitochondrial	SUCLA2	Homo sapiens (human)	0	1	3-methylglutaconic aciduria type 4 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 3 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Creutzfeldt-Jakob disease Crohn's colitis Crohn's disease Down syndrome Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Laron syndrome Leigh disease Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome achondroplasia age related macular degeneration alternating hemiplegia of childhood amnestic disorder amyloidosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autonomic neuropathy blindness central nervous system disease cerebral degeneration congenital ptosis congestive heart failure coronary artery disease cutaneous porphyria degeneration of macula and posterior pole dementia depressive disorder diabetes mellitus diabetic ketoacidosis dissociative amnesia dysthymic disorder dystonia enterocele epilepsy erythropoietic protoporphyria familial retinoblastoma focal hand dystonia frontotemporal dementia generalized dystonia herpes simplex hydrocephalus hypertropia inflammatory bowel disease 1 inflammatory bowel disease isolated elevated serum creatine phosphokinase levels lactic acidosis leukopenia lingual-facial-buccal dyskinesia macular degeneration major depressive disorder mechanical strabismus melancholic depression methylmalonic acidemia microcephaly mitochondrial DNA depletion syndrome 5 mitochondrial DNA depletion syndrome 9 mitochondrial DNA depletion syndrome mitochondrial encephalomyopathy movement disease nervous system disease neuroblastoma neurodegenerative disease neuropathy neurotic disorder obesity obsolete melancholia ophthalmoplegia parasitic helminthiasis infectious disease peripheral nervous system disease ptosis retinoblastoma retrocochlear disease retrograde amnesia sensorineural hearing loss sideroblastic anemia 1 strabismus trichohepatoenteric syndrome 1 trichohepatoenteric syndrome trilateral retinoblastoma tuberculosis type 2 diabetes mellitus ulcerative colitis vascular dementia visual epilepsy
Q9P2S2	Neurexin-2	NRXN2 KIAA0921	Homo sapiens (human)	8	5

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements