GlyCosmos Portal

Source	Last Updated
GlyConnect	March 24, 2025
GlycoProtDB	December 4, 2018
GlyGen	October 30, 2024
The O-GlcNAc Database	January 30, 2025
UniProt	February 20, 2025

Displaying entries **576 - 600** of **139028** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology ▲
P37275	Zinc finger E-box-binding homeobox 1	AREB6 TCF8 ZEB1	Homo sapiens (human)	2	0	Fuchs' endothelial dystrophy posterior polymorphous corneal dystrophy 3
P25318	Collagen alpha-2(VIII) chain	Col8a2	Mus musculus (house mouse)	2	0	Fuchs' endothelial dystrophy
Q96MI9	Cytosolic carboxypeptidase 4	AGBL1 CCP4	Homo sapiens (human)	1	1	Fuchs' endothelial dystrophy
O00755	Protein Wnt-7a	WNT7A	Homo sapiens (human)	3	0	Fuhrmann syndrome Schinzel type phocomelia
P24383	Protein Wnt-7a	Wnt-7a Wnt7a	Mus musculus (house mouse)	3	0	Fuhrmann syndrome
O75072	Ribitol-5-phosphate transferase FKTN	FCMD FKTN	Homo sapiens (human)	1	0	Fukuyama congenital muscular dystrophy Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M dilated cardiomyopathy 1B dilated cardiomyopathy 1X muscular dystrophy-dystroglycanopathy type B4 muscular dystrophy
Q8R507	Ribitol-5-phosphate transferase FKTN	Fcmd Fktn	Mus musculus (house mouse)	1	0	Fukuyama congenital muscular dystrophy muscular dystrophy-dystroglycanopathy type B1
Q8VHR5	Transcriptional repressor p66-beta	Gatad2b	Mus musculus (house mouse)	11	2	GAND syndrome
Q8WXI9	Transcriptional repressor p66-beta	GATAD2B KIAA1150	Homo sapiens (human)	21	2	GAND syndrome
Q9H6X2	Anthrax toxin receptor 1	ANTXR1 ATR TEM8	Homo sapiens (human)	4	2	GAPO syndrome colorectal carcinoma
P16278	Beta-galactosidase	ELNR1 GLB1	Homo sapiens (human)	7	81	GM1 gangliosidosis type 1 GM1 gangliosidosis type 2 GM1 gangliosidosis type 3 GM1 gangliosidosis mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis type IVB
P23780	Beta-galactosidase	Bgl Glb-1 Glb1	Mus musculus (house mouse)	8	0	GM1 gangliosidosis
P17900	Ganglioside GM2 activator	GM2A	Homo sapiens (human)	1	0	GM2 gangliosidosis, AB variant GM2 gangliosidosis
Q60648	Ganglioside GM2 activator	Gm2a	Mus musculus (house mouse)	1	0	GM2 gangliosidosis, AB variant
Q14657	EKC/KEOPS complex subunit LAGE3	DXS9879E ESO3 ITBA2 LAGE3	Homo sapiens (human)	2	2	Galloway-Mowat syndrome 2
Q9NPF4	tRNA N6-adenosine threonylcarbamoyltransferase	GCPL1 OSGEP	Homo sapiens (human)	2	1	Galloway-Mowat syndrome 3
P57740	Nuclear pore complex protein Nup107	NUP107	Homo sapiens (human)	9	2	Galloway-Mowat syndrome nephrotic syndrome type 11 ovarian dysgenesis 6
Q8WUM0	Nuclear pore complex protein Nup133	NUP133	Homo sapiens (human)	1	1	Galloway-Mowat syndrome nephrotic syndrome type 18
Q86U90	Threonylcarbamoyl-AMP synthase	DRIP3 IRIP YRDC	Homo sapiens (human)	3	2	Galloway-Mowat syndrome
P04062	Lysosomal acid glucosylceramidase	GBA GBA1 GC GLUC	Homo sapiens (human)	8	33	Gaucher's disease perinatal lethal Gaucher's disease type I Gaucher's disease type II Gaucher's disease type III Gaucher's disease type IIIC Gaucher's disease Lewy body dementia Parkinson's disease Parkinsonism late onset Parkinson's disease
A0A0G2JDK2	Glucosylceramidase	Gba Gba1	Mus musculus (house mouse)	3	0	Gaucher's disease type I Gaucher's disease type II Gaucher's disease
P30613	Pyruvate kinase PKLR	PK1 PKL PKLR	Homo sapiens (human)	1	0	Gaucher's disease congenital nonspherocytic hemolytic anemia 2 congenital nonspherocytic hemolytic anemia malaria type 2 diabetes mellitus
P21917	D(4) dopamine receptor	DRD4	Homo sapiens (human)	4	1	Gilles de la Tourette syndrome alcohol use disorder antisocial personality disorder attention deficit hyperactivity disorder cannabis abuse conduct disorder dyslexia heroin dependence intellectual disability liver cirrhosis nicotine dependence opioid abuse pathological gambling substance abuse
Q9UQB8	BAR/IMD domain-containing adapter protein 2	BAIAP2	Homo sapiens (human)	1	3	Gilles de la Tourette syndrome attention deficit hyperactivity disorder autism spectrum disorder
Q61327	Sodium-dependent dopamine transporter	Dat Dat1 Slc6a3	Mus musculus (house mouse)	4	0	Gilles de la Tourette syndrome attention deficit hyperactivity disorder schizophrenia

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