GlyCosmos Portal

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UniProt ID ▼	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9Y2I2	Netrin-G1	NTNG1 KIAA0976 LMNT1	4	2	Rett syndrome anorexia nervosa autistic disorder bipolar disorder brain disease cancer cerebral infarction cerebrovascular disease cocaine abuse cocaine dependence colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma epilepsy esophagitis gastroesophageal reflux disease head and neck squamous cell carcinoma hydrocephalus intellectual disability large intestine cancer learning disability lingual-facial-buccal dyskinesia microcephaly morphine dependence movement disease nephrolithiasis neuroendocrine carcinoma neuroendocrine tumor neuropathy patent ductus arteriosus peptic esophagitis peripheral nervous system disease polyneuropathy schizophrenia sensorineural hearing loss uric acid nephrolithiasis visual epilepsy
Q9Y2H9	Microtubule-associated serine/threonine-protein kinase 1	MAST1 KIAA0973 SAST	2	9
Q9Y2H5	Pleckstrin homology domain-containing family A member 6	PLEKHA6 KIAA0969 PEPP3	4	3
Q9Y2H2	Phosphatidylinositide phosphatase SAC2	INPP5F KIAA0966 SAC2	2	2	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease breast cancer diabetes mellitus diabetic ketoacidosis familial hyperlipidemia hyperglycemia type 2 diabetes mellitus
Q9Y2H0	Disks large-associated protein 4	DLGAP4 DAP4 KIAA0964 SAPAP4	2	2
Q9Y2G8	DnaJ homolog subfamily C member 16	DNAJC16 ERDJ8 KIAA0962	1	0
Q9Y2G7	Zinc finger protein 30 homolog	ZFP30 KIAA0961 ZNF745	2	1
Q9Y2G5	GDP-fucose protein O-fucosyltransferase 2	POFUT2 C21orf80 FUT13 KIAA0958	3	11	Peters plus syndrome congenital disorder of glycosylation malaria popliteal pterygium syndrome schizophrenia
Q9Y2G4	Ankyrin repeat domain-containing protein 6	ANKRD6 KIAA0957	1	1
Q9Y2G3	Phospholipid-transporting ATPase IF	ATP11B ATPIF ATPIR KIAA0956	1	1
Q9Y2G1	Myelin regulatory factor	MYRF C11orf9 KIAA0954 MRF	16	2
Q9Y2G0	Protein EFR3 homolog B	EFR3B KIAA0953	1	1
Q9Y2F5	Little elongation complex subunit 1	ICE1 KIAA0947	2	1
Q9Y2E8	Sodium/hydrogen exchanger 8	SLC9A8 KIAA0939 NHE8	2	1
Q9Y2E6	E3 ubiquitin-protein ligase DTX4	DTX4 KIAA0937 RNF155	2	1
Q9Y2E5	Epididymis-specific alpha-mannosidase	MAN2B2 KIAA0935	13	28	cerebral infarction cerebrovascular disease primary immunodeficiency disease
Q9Y2E4	Disco-interacting protein 2 homolog C	DIP2C KIAA0934	0	1
Q9Y2D9	Zinc finger protein 652	ZNF652 KIAA0924	3	1
Q9Y2D8	Afadin- and alpha-actinin-binding protein	SSX2IP KIAA0923	0	1
Q9Y2D5	PALM2-AKAP2 fusion protein	PALM2AKAP2 KIAA0920 PAKAP PALM2	1	1
Q9Y2D2	UDP-N-acetylglucosamine transporter	SLC35A3	0	1	Marfan syndrome autism spectrum disorder autistic disorder central nervous system cancer congenital disorder of glycosylation epilepsy gliosarcoma high grade glioma intellectual disability learning disability microcephaly mixed glioma mucopolysaccharidosis IV multiple epiphyseal dysplasia osteochondrodysplasia scoliosis situs inversus spondylocostal dysostosis syndromic X-linked intellectual disability 94 tuberous sclerosis visual epilepsy
Q9Y2D1	Cyclic AMP-dependent transcription factor ATF-5	ATF5 ATFX	0	1
Q9Y2D0	Carbonic anhydrase 5B, mitochondrial	CA5B	1	1
Q9Y2C9	Toll-like receptor 6	TLR6	9	2
Q9Y2C5	Probable small intestine urate exporter	SLC17A4	5	0

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