GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol ▼	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
P21453	Sphingosine 1-phosphate receptor 1	S1PR1 CHEDG1 EDG1	5	4
Q96BU1	S100P-binding protein	S100PBP S100PBPR	0	1
P25815	Protein S100-P	S100P S100E	0	1
P06702	Protein S100-A9	S100A9 CAGB CFAG MRP14	0	1
P05109	Protein S100-A8	S100A8 CAGA CFAG MRP8	0	1
Q86SG5	Protein S100-A7A	S100A7A S100A15 S100A7L1	0	1
P31151	Protein S100-A7	S100A7 PSOR1 S100A7C	0	1
P06703	Protein S100-A6	S100A6 CACY	0	1
P26447	Protein S100-A4	S100A4 CAPL MTS1	0	1
Q96FQ6	Protein S100-A16	S100A16 S100F	0	1
Q9HCY8	Protein S100-A14	S100A14 S100A15	0	1
Q99584	Protein S100-A13	S100A13	0	1
P31949	Protein S100-A11	S100A11 MLN70 S100C	0	1
P60903	Protein S100-A10	S100A10 ANX2LG CAL1L CLP11	0	1
Q15413	Ryanodine receptor 3	RYR3 HBRR	10	1
Q92736	Ryanodine receptor 2	RYR2	4	2
P21817	Ryanodine receptor 1	RYR1 RYDR	2	2
P34925	Tyrosine-protein kinase RYK	RYK JTK5A	5	0
G3V1K2	Ribitol xylosyltransferase 1	RXYLT1	1	0
Q9Y2B1	Ribitol-5-phosphate xylosyltransferase 1	RXYLT1 TMEM5	4	2	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Turner syndrome Walker-Warburg syndrome 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 disorder of glycosylation congenital muscular dystrophy-dystroglycanopathy type A10 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism distal myopathy epilepsy facioscapulohumeral muscular dystrophy fundus dystrophy glaucoma gonadal dysgenesis hydranencephaly hydrocephalus intellectual disability learning disability limb-girdle muscular dystrophy lissencephaly 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
P48443	Retinoic acid receptor RXR-gamma	RXRG NR2B3	0	1
P28702	Retinoic acid receptor RXR-beta	RXRB NR2B2	0	1
P19793	Retinoic acid receptor RXR-alpha	RXRA NR2B1	0	1
Q8TDU9	Relaxin-3 receptor 2	RXFP4 GPCR142 GPR100 RLN3R2	2	0
Q9NSD7	Relaxin-3 receptor 1	RXFP3 GPCR135 RLN3R1 SALPR	2	0

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