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 **576 - 600** 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
Q9Y320	Thioredoxin-related transmembrane protein 2	TMX2 TXNDC14	Homo sapiens (human)	1	2
Q9Y316	Protein MEMO1	MEMO1 C2orf4 MEMO NS5ATP7	Homo sapiens (human)	0	1
Q9Y314	Nitric oxide synthase-interacting protein	NOSIP	Homo sapiens (human)	4	3
Q9Y312	Protein AAR2 homolog	AAR2 C20orf4	Homo sapiens (human)	0	1
Q9Y305	Acyl-coenzyme A thioesterase 9, mitochondrial	ACOT9	Homo sapiens (human)	0	1
Q9Y2Z9	Ubiquinone biosynthesis monooxygenase COQ6, mitochondrial	COQ6	Homo sapiens (human)	1	1
Q9Y2Z4	Tyrosine--tRNA ligase, mitochondrial	YARS2	Homo sapiens (human)	1	1
Q9Y2Z2	Protein MTO1 homolog, mitochondrial	MTO1	Homo sapiens (human)	1	2
Q9Y2Z0	Protein SGT1 homolog	SUGT1	Homo sapiens (human)	2	4
Q9Y2Y4	Zinc finger and BTB domain-containing protein 32	ZBTB32 FAZF TZFP ZNF538	Homo sapiens (human)	2	1
Q9Y2Y1	DNA-directed RNA polymerase III subunit RPC10	POLR3K RPC11	Homo sapiens (human)	0	1
Q9Y2X9	Zinc finger protein 281	ZNF281 GZP1 ZBP99	Homo sapiens (human)	30	2
Q9Y2X7	ARF GTPase-activating protein GIT1	GIT1	Homo sapiens (human)	4	2
Q9Y2X3	Nucleolar protein 58	NOP58 NOL5 NOP5	Homo sapiens (human)	1	1
Q9Y2X0	Mediator of RNA polymerase II transcription subunit 16	MED16 DRIP92 THRAP5	Homo sapiens (human)	1	1
Q9Y2W2	WW domain-binding protein 11	WBP11 NPWBP SIPP1 SNP70	Homo sapiens (human)	3	1
Q9Y2W1	Thyroid hormone receptor-associated protein 3	THRAP3 BCLAF2 TRAP150	Homo sapiens (human)	8	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
Q9Y2V2	Calcium-regulated heat-stable protein 1	CARHSP1	Homo sapiens (human)	0	1
Q9Y2U8	Inner nuclear membrane protein Man1	LEMD3 MAN1	Homo sapiens (human)	5	7
Q9Y2U2	Potassium channel subfamily K member 7	KCNK7	Homo sapiens (human)	1	0
Q9Y2T7	Y-box-binding protein 2	YBX2 CSDA3 MSY2	Homo sapiens (human)	1	1
Q9Y2T6	G-protein coupled receptor 55	GPR55	Homo sapiens (human)	2	0
Q9Y2T5	G-protein coupled receptor 52	GPR52	Homo sapiens (human)	3	0
Q9Y2T3	Guanine deaminase	GDA KIAA1258	Homo sapiens (human)	1	2

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