GlyCosmos Portal

Displaying entries **17026 - 17050** of **18496** in total

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UniProt ID ▲	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9NYV4	Cyclin-dependent kinase 12	CDK12 CRK7 CRKRS KIAA0904	16	3
Q9NYV7	Taste receptor type 2 member 16	TAS2R16	2	0
Q9NYV8	Taste receptor type 2 member 14	TAS2R14	3	0
Q9NYV9	Taste receptor type 2 member 13	TAS2R13	2	0
Q9NYW0	Taste receptor type 2 member 10	TAS2R10	2	0
Q9NYW1	Taste receptor type 2 member 9	TAS2R9	1	0
Q9NYW2	Taste receptor type 2 member 8	TAS2R8	1	0
Q9NYW3	Taste receptor type 2 member 7	TAS2R7	2	0
Q9NYW4	Taste receptor type 2 member 5	TAS2R5	1	0
Q9NYW5	Taste receptor type 2 member 4	TAS2R4	3	0
Q9NYW6	Taste receptor type 2 member 3	TAS2R3	1	0
Q9NYW7	Taste receptor type 2 member 1	TAS2R1	1	0
Q9NYX4	Neuron-specific vesicular protein calcyon	CALY DRD1IP	1	0
Q9NYY1	Interleukin-20	IL20 ZCYTO10	1	1
Q9NYZ3	G2 and S phase-expressed protein 1	GTSE1	1	2
Q9NYZ4	Sialic acid-binding Ig-like lectin 8	SIGLEC8 SAF2	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
Q9NZ01	Very-long-chain enoyl-CoA reductase	TECR GPSN2 SC2	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
Q9NZ08	Endoplasmic reticulum aminopeptidase 1	ERAP1 APPILS ARTS1 KIAA0525	8	32
Q9NZ09	Ubiquitin-associated protein 1	UBAP1	1	1
Q9NZ20	Group 3 secretory phospholipase A2	PLA2G3	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
Q9NZ32	Actin-related protein 10	ACTR10 ACTR11 ARP10 ARP11	0	1
Q9NZ45	CDGSH iron-sulfur domain-containing protein 1	CISD1 C10orf70 ZCD1	0	1
Q9NZ52	ADP-ribosylation factor-binding protein GGA3	GGA3 KIAA0154	4	1
Q9NZ53	Podocalyxin-like protein 2	PODXL2	18	8
Q9NZ56	Formin-2	FMN2	0	1

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