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 **8576 - 8600** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
Q9UFB7	Zinc finger and BTB domain-containing protein 47	ZBTB47 KIAA1190 ZNF651	Homo sapiens (human)	1
Q53GT1	Kelch-like protein 22	KLHL22	Homo sapiens (human)	1
K2PBQ1	Mitochondrial exoribonuclease DSS-1, putative	MOQ_001260	Trypanosoma cruzi marinkellei	1
V5BG04	DNA topoisomerase	TCDM_04626	Trypanosoma cruzi Dm28c	1
Q14596	Next to BRCA1 gene 1 protein	NBR1 1A13B KIAA0049 M17S2	Homo sapiens (human)	4
Q9CQ43	Deoxyuridine 5'-triphosphate nucleotidohydrolase	Dut Dutp	Mus musculus (house mouse)	1
O00244	Copper transport protein ATOX1	ATOX1 HAH1	Homo sapiens (human)	1
P62308	Small nuclear ribonucleoprotein G	SNRPG PBSCG	Homo sapiens (human)	1
P00920	Carbonic anhydrase 2	Ca2 Car2	Mus musculus (house mouse)	1
Q3B726	DNA-directed RNA polymerase I subunit RPA43	POLR1F TWISTNB	Homo sapiens (human)	1
O61066	Cathepsin B-like protease	tccb	Trypanosoma cruzi	1
Q8TC21	Zinc finger protein 596	ZNF596	Homo sapiens (human)	1
V5BWE8	ATPase ASNA1 homolog	TCDM_00659	Trypanosoma cruzi Dm28c	1
Q86W11	Zinc finger and SCAN domain-containing protein 30	ZSCAN30 ZNF397OS	Homo sapiens (human)	1
P29172	Microtubule-associated protein tau	MAPT TAU	Bos taurus (cattle)	1
Q9SK04	Uncharacterized protein At2g28540	At2g28540	Arabidopsis thaliana (thale cress)	1
Q9NPC8	Homeobox protein SIX2	SIX2	Homo sapiens (human)	1
O00160	Unconventional myosin-If	MYO1F	Homo sapiens (human)	1
Q4DJ19	35 kDa cyclophilin, putative	Tc00.1047053504797.100	Trypanosoma cruzi strain CL Brener	1
P02088	Hemoglobin subunit beta-1	Hbb-b1	Mus musculus (house mouse)	1
Q92882	Osteoclast-stimulating factor 1	OSTF1	Homo sapiens (human)	1
Q6P5B0	RRP12-like protein	Rrp12 Kiaa0690	Mus musculus (house mouse)	1
Q9P2R7	Succinate--CoA ligase [ADP-forming] subunit beta, mitochondrial	SUCLA2	Homo sapiens (human)	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
Q96JG6	Syndetin	VPS50 CCDC132 KIAA1861	Homo sapiens (human)	1
Q4CQ54	[phosphatase 2A protein]-leucine-carboxy methyltransferase (Fragment)	Tc00.1047053508463.29	Trypanosoma cruzi strain CL Brener	1

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