GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
P63244	Small ribosomal subunit protein RACK1	RACK1 GNB2L1	5	1
P58004	Sestrin-2	SESN2 Hi95 SEST2	1	1
Q9NU22	Midasin	MDN1 KIAA0301	5	11
Q6P158	Putative ATP-dependent RNA helicase DHX57	DHX57	2	1
P12034	Fibroblast growth factor 5	FGF5	3	1
Q13145	BMP and activin membrane-bound inhibitor homolog	BAMBI NMA	4	2
D5FI31	MHC class I antigen (Fragment)	HLA-B	1	0
Q9H2X6	Homeodomain-interacting protein kinase 2	HIPK2	6	3
Q6TFL4	Kelch-like protein 24	KLHL24 DRE1	0	1
A0A2U7MWK8	MHC class I antigen (Fragment)	HLA-C	1	0
A0A186VN67	MHC class I antigen (Fragment)	HLA-C	1	0
O15084	Serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A	ANKRD28 KIAA0379	2	2
Q12980	GATOR1 complex protein NPRL3	NPRL3 C16orf35 CGTHBA MARE	2	3
F1AQR0	MHC class I antigen (Fragment)	HLA-C	1	0
Q860I7	MHC class I antigen	HLA-B	1	0
P14921	Protein C-ets-1	ETS1 EWSR2	0	1
P0DO97	Coiled-coil domain-containing protein 192	CCDC192 LINC01183	2	1
P34995	Prostaglandin E2 receptor EP1 subtype	PTGER1	2	0
A0A6B7FTQ6	MHC class I antigen	HLA-B	1	0
Q9H1X1	Radial spoke head protein 9 homolog	RSPH9 C6orf206 MRPS18AL1	0	1
Q92508	Piezo-type mechanosensitive ion channel component 1	PIEZO1 FAM38A KIAA0233	3	10
B2YG98	MHC class I antigen (Fragment)	HLA-B	1	0
Q8NAT1	Protein O-linked-mannose beta-1,4-N-acetylglucosaminyltransferase 2	POMGNT2 AGO61 C3orf39 EOGTL GTDC2	6	8	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome acute myeloid leukemia autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy cataract coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A8 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism distal myopathy epilepsy facioscapulohumeral muscular dystrophy fundus dystrophy glaucoma hydranencephaly hydrocephalus intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly malaria microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obstructive hydrocephalus oculopharyngeal muscular dystrophy optic atrophy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal detachment rippling muscle disease 2 senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly syndromic X-linked intellectual disability Najm type visual epilepsy
O95297	Myelin protein zero-like protein 1	MPZL1 PZR	5	55
P0C0S8	Histone H2A type 1	H2AC11 H2AC13 H2AC15 H2AC16 H2AC17 H2AFC H2AFD H2AFI H2AFN H2AFP HIST1H2AG HIST1H2AI HIST1H2AK HIST1H2AL HIST1H2AM	1	1

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