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 **2051 - 2075** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol ▼	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q8IWZ8	SURP and G-patch domain-containing protein 1	SUGP1 SF4	Homo sapiens (human)	8	2
Q9HAC7	Succinate--hydroxymethylglutarate CoA-transferase	SUGCT C7orf10 DERP13	Homo sapiens (human)	0	1
Q9H7L9	Sin3 histone deacetylase corepressor complex component SDS3	SUDS3 SAP45 SDS3	Homo sapiens (human)	1	1
Q9UBS9	SUN domain-containing ossification factor	SUCO C1orf9 CH1 OPT SLP1	Homo sapiens (human)	14	15
Q9BXA5	Succinate receptor 1	SUCNR1 GPR91	Homo sapiens (human)	2	0
Q96I99	Succinate--CoA ligase [GDP-forming] subunit beta, mitochondrial	SUCLG2	Homo sapiens (human)	0	1	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 Pick's disease Reye syndrome cerebral degeneration endometriosis of ovary endometriosis methylmalonic acidemia prostate cancer prostate carcinoma
P53597	Succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial	SUCLG1	Homo sapiens (human)	1	1	Leigh disease McCune Albright syndrome brain disease cardiomyopathy central nervous system cancer cerebral degeneration endomyocardial fibrosis epilepsy familial hypertrophic cardiomyopathy giant cell glioblastoma glioblastoma gliosarcoma high grade glioma hypertrophic cardiomyopathy hypoglycemia hypophosphatemia intellectual disability lactic acidosis learning disability methylmalonic acidemia mitochondrial DNA depletion syndrome 5 mitochondrial DNA depletion syndrome 9 mitochondrial DNA depletion syndrome mitochondrial encephalomyopathy mixed glioma skin disease stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 visual epilepsy
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
P53999	Activated RNA polymerase II transcriptional coactivator p15	SUB1 PC4 RPO2TC1	Homo sapiens (human)	3	1
Q9Y6J8	Serine/threonine/tyrosine-interacting-like protein 1	STYXL1 DUSP24 MKSTYX	Homo sapiens (human)	0	1
Q8WUJ0	Serine/threonine/tyrosine-interacting protein	STYX	Homo sapiens (human)	0	1
Q8NFX7	Syntaxin-binding protein 6	STXBP6	Homo sapiens (human)	1	1
Q6ZWJ1	Syntaxin-binding protein 4	STXBP4	Homo sapiens (human)	0	1
Q15833	Syntaxin-binding protein 2	STXBP2 UNC18B	Homo sapiens (human)	1	1
P61764	Syntaxin-binding protein 1	STXBP1 UNC18A	Homo sapiens (human)	1	1
O15400	Syntaxin-7	STX7	Homo sapiens (human)	0	1
O43752	Syntaxin-6	STX6	Homo sapiens (human)	0	1
Q13190	Syntaxin-5	STX5 STX5A	Homo sapiens (human)	0	1
Q12846	Syntaxin-4	STX4 STX4A	Homo sapiens (human)	0	1
P61266	Syntaxin-1B	STX1B STX1B1 STX1B2	Homo sapiens (human)	0	1
Q16623	Syntaxin-1A	STX1A STX1	Homo sapiens (human)	1	1
P56962	Syntaxin-17	STX17	Homo sapiens (human)	0	1
O14662	Syntaxin-16	STX16	Homo sapiens (human)	0	1
Q86Y82	Syntaxin-12	STX12	Homo sapiens (human)	0	1
Q9UNE7	E3 ubiquitin-protein ligase CHIP	STUB1 CHIP	Homo sapiens (human)	0	1

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