GlyCosmos Portal

Displaying entries **3951 - 3975** of **18496** in total

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UniProt ID	Protein Name ▲	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9Y613	FH1/FH2 domain-containing protein 1	FHOD1 FHOS FHOS1	1	1
Q2V2M9	FH1/FH2 domain-containing protein 3	FHOD3 FHOS2 KIAA1695	1	1
Q5W0V3	FHF complex subunit HOOK interacting protein 2A	FHIP2A FAM160B1 KIAA1600	0	1
Q5T1M5	FK506-binding protein 15	FKBP15 KIAA0674	5	1
Q8NF19	FLJ00383 protein (Fragment)	FLJ00383	1	0
Q96CP2	FLYWCH family member 2	FLYWCH2	1	1
Q9UHK0	FMR1-interacting protein NUFIP1	NUFIP1	0	1
Q7Z417	FMR1-interacting protein NUFIP2	NUFIP2 KIAA1321	21	5
Q6ZUU3	FOXL2 neighbor protein	FOXL2NB C3orf72	2	1
Q05CW8	FRAS1 protein (Fragment)	FRAS1	1	0
Q5H8C1	FRAS1-related extracellular matrix protein 1	FREM1 C9orf143 C9orf145 C9orf154	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
Q5SZK8	FRAS1-related extracellular matrix protein 2	FREM2	9	47
P0C091	FRAS1-related extracellular matrix protein 3	FREM3	4	0
Q9BWH2	FUN14 domain-containing protein 2	FUNDC2 HCBP6	0	1
Q96DB9	FXYD domain-containing ion transport regulator 5	FXYD5 DYSAD IWU1	15	4
P58549	FXYD domain-containing ion transport regulator 7	FXYD7	3	0
O15117	FYN-binding protein 1	FYB1 FYB SLAP130	5	2
Q9BQS8	FYVE and coiled-coil domain-containing protein 1	FYCO1 ZFYVE7	0	1
Q5JSP0	FYVE, RhoGEF and PH domain-containing protein 3	FGD3 ZFYVE5	0	1
Q6ZNL6	FYVE, RhoGEF and PH domain-containing protein 5	FGD5 ZFYVE23	3	1
Q6ZV73	FYVE, RhoGEF and PH domain-containing protein 6	FGD6 KIAA1362 ZFYVE24	0	1
B4DGG1	Family with sequence similarity 234 member A	FAM234A	2	0
H7C2U8	Family with sequence similarity 234 member A (Fragment)	FAM234A	1	0
A0A0A8K9B4	Family with sequence similarity 3, member D	FAM3D	1	0
Q0VG06	Fanconi anemia core complex-associated protein 100	FAAP100 C17orf70	1	1

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