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 **5401 - 5425** 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
Q9Y2I7	1-phosphatidylinositol 3-phosphate 5-kinase	PIKFYVE KIAA0981 PIP5K3	Homo sapiens (human)	4	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 B-cell lymphoma Crohn's colitis Crohn's disease Fleck corneal dystrophy Pick's disease Reye syndrome breast cancer cancer cardiomyopathy cerebral degeneration embryoma endomyocardial fibrosis gestational diabetes hypertrophic cardiomyopathy legionellosis multiple myeloma obsolete asthenopia obsolete ymphosarcoma pneumonia transitional cell carcinoma
Q9Y2I6	Ninein-like protein	NINL KIAA0980 NLP	Homo sapiens (human)	0	1
Q9Y2I2	Netrin-G1	NTNG1 KIAA0976 LMNT1	Homo sapiens (human)	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	Homo sapiens (human)	2	9
Q9Y2H5	Pleckstrin homology domain-containing family A member 6	PLEKHA6 KIAA0969 PEPP3	Homo sapiens (human)	4	3
Q9Y2H2	Phosphatidylinositide phosphatase SAC2	INPP5F KIAA0966 SAC2	Homo sapiens (human)	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	Homo sapiens (human)	2	2
Q9Y2G8	DnaJ homolog subfamily C member 16	DNAJC16 ERDJ8 KIAA0962	Homo sapiens (human)	1	0
Q9Y2G7	Zinc finger protein 30 homolog	ZFP30 KIAA0961 ZNF745	Homo sapiens (human)	2	1
Q9Y2G5	GDP-fucose protein O-fucosyltransferase 2	POFUT2 C21orf80 FUT13 KIAA0958	Homo sapiens (human)	3	11	Peters plus syndrome congenital disorder of glycosylation malaria popliteal pterygium syndrome schizophrenia
Q9Y2G4	Ankyrin repeat domain-containing protein 6	ANKRD6 KIAA0957	Homo sapiens (human)	1	1
Q9Y2G3	Phospholipid-transporting ATPase IF	ATP11B ATPIF ATPIR KIAA0956	Homo sapiens (human)	1	1
Q9Y2G1	Myelin regulatory factor	MYRF C11orf9 KIAA0954 MRF	Homo sapiens (human)	16	2
Q9Y2G0	Protein EFR3 homolog B	EFR3B KIAA0953	Homo sapiens (human)	1	1
Q9Y2F5	Little elongation complex subunit 1	ICE1 KIAA0947	Homo sapiens (human)	2	1
Q9Y2E8	Sodium/hydrogen exchanger 8	SLC9A8 KIAA0939 NHE8	Homo sapiens (human)	2	1
Q9Y2E6	E3 ubiquitin-protein ligase DTX4	DTX4 KIAA0937 RNF155	Homo sapiens (human)	2	1
Q9Y2E5	Epididymis-specific alpha-mannosidase	MAN2B2 KIAA0935	Homo sapiens (human)	13	28	cerebral infarction cerebrovascular disease primary immunodeficiency disease
Q9Y2E4	Disco-interacting protein 2 homolog C	DIP2C KIAA0934	Homo sapiens (human)	0	1
Q9Y2D9	Zinc finger protein 652	ZNF652 KIAA0924	Homo sapiens (human)	3	1
Q9Y2D8	Afadin- and alpha-actinin-binding protein	SSX2IP KIAA0923	Homo sapiens (human)	0	1
Q9Y2D5	PALM2-AKAP2 fusion protein	PALM2AKAP2 KIAA0920 PAKAP PALM2	Homo sapiens (human)	1	1
Q9Y2D2	UDP-N-acetylglucosamine transporter	SLC35A3	Homo sapiens (human)	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	Homo sapiens (human)	0	1
Q9Y2D0	Carbonic anhydrase 5B, mitochondrial	CA5B	Homo sapiens (human)	1	1

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