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 **7951 - 7975** of **126547** in total

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UniProt ID ▼	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9NZC2	Triggering receptor expressed on myeloid cells 2	TREM2	Homo sapiens (human)	2	0
Q9NZB2	Constitutive coactivator of PPAR-gamma-like protein 1	FAM120A C9orf10 KIAA0183 OSSA	Homo sapiens (human)	1	2
Q9NZ94	Neuroligin-3	NLGN3 KIAA1480 NL3	Homo sapiens (human)	2	0
Q9NZ71	Regulator of telomere elongation helicase 1	RTEL1 C20orf41 KIAA1088 NHL	Homo sapiens (human)	0	1
Q9NZ63	Splicing factor C9orf78	C9orf78 HCA59	Homo sapiens (human)	0	1
Q9NZ56	Formin-2	FMN2	Homo sapiens (human)	0	1
Q9NZ53	Podocalyxin-like protein 2	PODXL2	Homo sapiens (human)	18	8
Q9NZ52	ADP-ribosylation factor-binding protein GGA3	GGA3 KIAA0154	Homo sapiens (human)	4	1
Q9NZ45	CDGSH iron-sulfur domain-containing protein 1	CISD1 C10orf70 ZCD1	Homo sapiens (human)	0	1
Q9NZ32	Actin-related protein 10	ACTR10 ACTR11 ARP10 ARP11	Homo sapiens (human)	0	1
Q9NZ20	Group 3 secretory phospholipase A2	PLA2G3	Homo sapiens (human)	5	3	acute myocardial infarction cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary thrombosis embryoma large intestine cancer myocardial infarction silent myocardial infarction
Q9NZ09	Ubiquitin-associated protein 1	UBAP1	Homo sapiens (human)	1	1
Q9NZ08	Endoplasmic reticulum aminopeptidase 1	ERAP1 APPILS ARTS1 KIAA0525	Homo sapiens (human)	8	32
Q9NZ01	Very-long-chain enoyl-CoA reductase	TECR GPSN2 SC2	Homo sapiens (human)	2	1	Marfan syndrome agnosia autosomal recessive intellectual developmental disorder cardiovascular system disease cerebral degeneration choreatic disease depressive disorder developmental coordination disorder dyskeratosis congenita dysthymic disorder dystonia endometriosis of uterus endometriosis epilepsy focal epilepsy heart disease influenza intellectual disability learning disability lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia partial motor epilepsy pneumothorax situs inversus stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 tuberous sclerosis visual epilepsy
Q9NYZ4	Sialic acid-binding Ig-like lectin 8	SIGLEC8 SAF2	Homo sapiens (human)	3	27	Hirschsprung's disease Loeffler syndrome allergic asthma anisakiasis asthma cancer chronic obstructive pulmonary disease colitis eosinophilic esophagitis eosinophilic gastritis eosinophilic gastroenteritis eosinophilic pneumonia gastritis gastroenteritis hypereosinophilic syndrome ileitis ileocolitis intrinsic asthma pneumonia pulmonary eosinophilia
Q9NYZ3	G2 and S phase-expressed protein 1	GTSE1	Homo sapiens (human)	1	2
Q9NYY1	Interleukin-20	IL20 ZCYTO10	Homo sapiens (human)	1	1
Q9NYX4	Neuron-specific vesicular protein calcyon	CALY DRD1IP	Homo sapiens (human)	1	0
Q9NYW7	Taste receptor type 2 member 1	TAS2R1	Homo sapiens (human)	1	0
Q9NYW6	Taste receptor type 2 member 3	TAS2R3	Homo sapiens (human)	1	0
Q9NYW5	Taste receptor type 2 member 4	TAS2R4	Homo sapiens (human)	3	0
Q9NYW4	Taste receptor type 2 member 5	TAS2R5	Homo sapiens (human)	1	0
Q9NYW3	Taste receptor type 2 member 7	TAS2R7	Homo sapiens (human)	2	0
Q9NYW2	Taste receptor type 2 member 8	TAS2R8	Homo sapiens (human)	1	0
Q9NYW1	Taste receptor type 2 member 9	TAS2R9	Homo sapiens (human)	1	0

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