GlyCosmos Portal

Displaying entries **76 - 100** of **10713** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology ▲
P28654	Decorin	Dcn	5	5	Ehlers-Danlos syndrome congenital stromal corneal dystrophy
Q99LL6	Col1a1 protein (Fragment)	Col1a1	1	0	Ehlers-Danlos syndrome osteogenesis imperfecta type 1 osteogenesis imperfecta type 2 osteogenesis imperfecta type 3 osteogenesis imperfecta type 4 osteogenesis imperfecta
A8Y5E6	Procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1	Plod1	1	0	Ehlers-Danlos syndrome
Q8K1G2	Limbin	Evc2 Lbn	5	2	Ellis-Van Creveld syndrome
P57680	EvC complex member EVC	Evc	1	1	Ellis-Van Creveld syndrome
Q6ZWR6	Nesprin-1	Syne1	7	5	Emery-Dreifuss muscular dystrophy
Q8BGZ6	Alpha-galactosidase	Gla	2	0	Fabry disease
Q9JL70	Fanconi anemia group A protein homolog	Fanca	2	1	Fanconi anemia complementation group A
Q9WV54	Acid ceramidase	Asah Asah1	5	12	Farber lipogranulomatosis
Q684R7	FRAS1-related extracellular matrix protein 1	Frem1	6	0	Fraser syndrome chromosome 9p deletion syndrome congenital diaphragmatic hernia
Q925T6	Glutamate receptor-interacting protein 1	Grip1	3	3	Fraser syndrome clubfoot recessive dystrophic epidermolysis bullosa
Q80T14	Extracellular matrix organizing protein FRAS1	Fras1 Kiaa1500	21	4	Fraser syndrome clubfoot
Q1XGY5	Fras1 related extracellular matrix protein 2	Frem2	2	0	Fraser syndrome isolated cryptophthalmia
P25318	Collagen alpha-2(VIII) chain	Col8a2	2	0	Fuchs' endothelial dystrophy
P24383	Protein Wnt-7a	Wnt-7a Wnt7a	3	0	Fuhrmann syndrome
Q8R507	Ribitol-5-phosphate transferase FKTN	Fcmd Fktn	1	0	Fukuyama congenital muscular dystrophy muscular dystrophy-dystroglycanopathy type B1
Q8VHR5	Transcriptional repressor p66-beta	Gatad2b	11	2	GAND syndrome
P23780	Beta-galactosidase	Bgl Glb-1 Glb1	8	0	GM1 gangliosidosis
Q60648	Ganglioside GM2 activator	Gm2a	1	0	GM2 gangliosidosis, AB variant
A0A0G2JDK2	Glucosylceramidase	Gba Gba1	3	0	Gaucher's disease type I Gaucher's disease type II Gaucher's disease
Q61327	Sodium-dependent dopamine transporter	Dat Dat1 Slc6a3	4	0	Gilles de la Tourette syndrome attention deficit hyperactivity disorder schizophrenia
P16056	Hepatocyte growth factor receptor	Met	13	0	Gilles de la Tourette syndrome autism spectrum disorder breast cancer gestational diabetes
Q69Z70	MKIAA1910 protein (Fragment)	Slitrk1 mKIAA1910	1	0	Gilles de la Tourette syndrome
Q80UE6	Serine/threonine-protein kinase WNK4	Prkwnk4 Wnk4	8	1	Gitelman syndrome pseudohypoaldosteronism
P59158	Solute carrier family 12 member 3	Ncc Slc12a3 Tsc	2	0	Gitelman syndrome

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