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 **14526 - 14550** 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
Q6ZV73	FYVE, RhoGEF and PH domain-containing protein 6	FGD6 KIAA1362 ZFYVE24	Homo sapiens (human)	0	1
Q6ZNL6	FYVE, RhoGEF and PH domain-containing protein 5	FGD5 ZFYVE23	Homo sapiens (human)	3	1
Q5JSP0	FYVE, RhoGEF and PH domain-containing protein 3	FGD3 ZFYVE5	Homo sapiens (human)	0	1
Q9BQS8	FYVE and coiled-coil domain-containing protein 1	FYCO1 ZFYVE7	Homo sapiens (human)	0	1
O15117	FYN-binding protein 1	FYB1 FYB SLAP130	Homo sapiens (human)	5	2
P58549	FXYD domain-containing ion transport regulator 7	FXYD7	Homo sapiens (human)	3	0
Q96DB9	FXYD domain-containing ion transport regulator 5	FXYD5 DYSAD IWU1	Homo sapiens (human)	15	4
Q9BWH2	FUN14 domain-containing protein 2	FUNDC2 HCBP6	Homo sapiens (human)	0	1
P0C091	FRAS1-related extracellular matrix protein 3	FREM3	Homo sapiens (human)	4	0
Q5SZK8	FRAS1-related extracellular matrix protein 2	FREM2	Homo sapiens (human)	9	47
Q5H8C1	FRAS1-related extracellular matrix protein 1	FREM1 C9orf143 C9orf145 C9orf154	Homo sapiens (human)	7	4	3p deletion syndrome Angelman syndrome Baraitser-Winter syndrome CAKUT Fraser syndrome 1 Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome NFIA-related disorder Nance-Horan syndrome Potter's syndrome SATB2-associated syndrome Sakati-Nyhan syndrome Smith-Magenis syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome acquired immunodeficiency syndrome anorectal stricture bilateral renal aplasia branchiootic syndrome cardiovascular system disease chromosome 13q14 deletion syndrome chromosome 15q13.3 microdeletion syndrome chromosome 15q24 deletion syndrome chromosome 15q26-qter deletion syndrome chromosome 16p11.2 deletion syndrome, 220-kb chromosome 16p12.2-p11.2 deletion syndrome chromosome 17q12 deletion syndrome chromosome 17q23.1-q23.2 deletion syndrome chromosome 18q deletion syndrome chromosome 1q21.1 deletion syndrome chromosome 1q41-q42 deletion syndrome chromosome 2p16.1-p15 deletion syndrome chromosome 6pter-p24 deletion syndrome chromosome 8q21.11 deletion syndrome chromosome 9p deletion syndrome congenital diaphragmatic hernia craniosynostosis distal 10q deletion syndrome eye disease heart disease hiatus hernia human immunodeficiency virus infectious disease microphthalmia myelofibrosis omphalocele orofaciodigital syndrome I orofaciodigital syndrome X rectal prolapse renal agenesis umbilical hernia
Q05CW8	FRAS1 protein (Fragment)	FRAS1	Homo sapiens (human)	1	0
Q6ZUU3	FOXL2 neighbor protein	FOXL2NB C3orf72	Homo sapiens (human)	2	1
Q7Z417	FMR1-interacting protein NUFIP2	NUFIP2 KIAA1321	Homo sapiens (human)	21	5
Q9UHK0	FMR1-interacting protein NUFIP1	NUFIP1	Homo sapiens (human)	0	1
Q96CP2	FLYWCH family member 2	FLYWCH2	Homo sapiens (human)	1	1
Q8NF19	FLJ00383 protein (Fragment)	FLJ00383	Homo sapiens (human)	1	0
Q5T1M5	FK506-binding protein 15	FKBP15 KIAA0674	Homo sapiens (human)	5	1
Q5W0V3	FHF complex subunit HOOK interacting protein 2A	FHIP2A FAM160B1 KIAA1600	Homo sapiens (human)	0	1
Q2V2M9	FH1/FH2 domain-containing protein 3	FHOD3 FHOS2 KIAA1695	Homo sapiens (human)	1	1
Q9Y613	FH1/FH2 domain-containing protein 1	FHOD1 FHOS FHOS1	Homo sapiens (human)	1	1
A0PJ49	FGFRL1 protein (Fragment)	FGFRL1	Homo sapiens (human)	1	0
Q9NVK5	FGFR1 oncogene partner 2	FGFR1OP2	Homo sapiens (human)	0	1
O94887	FERM, ARHGEF and pleckstrin domain-containing protein 2	FARP2 KIAA0793 PLEKHC3	Homo sapiens (human)	0	1
Q6ZUT3	FERM domain-containing protein 7	FRMD7	Homo sapiens (human)	0	1

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