GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (9988) Glycans (5831) Glycoproteins (15733) Lectins (298) Pathways (2074)

Displaying entries **3001 - 3025** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
116113	forkhead box P4	FOXP4
80020	FAD dependent oxidoreductase domain containing 2	FOXRED2
8790	fucose-1-phosphate guanylyltransferase	FPGT GFPP	chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
2357	formyl peptide receptor 1	FPR1
2358	formyl peptide receptor 2	FPR2
2359	formyl peptide receptor 3	FPR3
80144	Fraser extracellular matrix complex subunit 1	FRAS1
158326	FRAS1 related extracellular matrix 1	FREM1 C9orf143 C9orf145 DKFZp686M16108 FLJ25461 TILRR	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
341640	FRAS1 related extracellular matrix 2	FREM2
166752	FRAS1 related extracellular matrix 3	FREM3
23150	FERM domain containing 4B	FRMD4B
9758	FERM and PDZ domain containing 4	FRMPD4
391059	ferric chelate reductase 1	FRRS1
10818	fibroblast growth factor receptor substrate 2	FRS2
10817	fibroblast growth factor receptor substrate 3	FRS3
10129	FRY microtubule binding protein	FRY
285527	FRY like transcription coactivator	FRYL
2487	frizzled related protein	FRZB
128061	40S small subunit processome assembly factor 1	FSAF1
6624	fascin actin-bundling protein 1	FSCN1
2488	follicle stimulating hormone subunit beta	FSHB
2492	follicle stimulating hormone receptor	FSHR
161835	fibrous sheath interacting protein 1	FSIP1
401024	fibrous sheath interacting protein 2	FSIP2
10468	follistatin	FST

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