GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
D6MLG2	MHC class I antigen (Fragment)	HLA-C	1	0
A0A087WW63	Voltage-dependent P/Q-type calcium channel subunit alpha	CACNA1A	1	0
H0YIH3	Decorin (Fragment)	DCN	1	0
P32189	Glycerol kinase	GK	1	1	Aland Island eye disease Becker muscular dystrophy Duchenne muscular dystrophy Kallmann syndrome Klinefelter syndrome Laron syndrome Patau syndrome Sheehan syndrome X-linked adrenal hypoplasia congenita achondroplasia 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 chromosome Xp21 deletion syndrome cone-rod dystrophy congenital muscular dystrophy coronary artery disease diabetes mellitus distal myopathy endomyocardial fibrosis facioscapulohumeral muscular dystrophy familial hypercholesterolemia fundus albipunctatus galactokinase deficiency galactosemia glycerol kinase deficiency hypertropia hypoglycemia hypogonadism hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism intellectual disability isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency learning disability limb-girdle muscular dystrophy mechanical strabismus muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 obesity 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 oculopharyngeal muscular dystrophy ophthalmoplegia osteoporosis panhypopituitarism placental insufficiency retinitis pigmentosa rippling muscle disease 2 strabismus tuberculosis type 2 diabetes mellitus
D3Y5Z0	MHC class I antigen (Fragment)	HLA-B	1	0
K7EPS5	Asialoglycoprotein receptor 1 (Fragment)	ASGR1	1	0
P41595	5-hydroxytryptamine receptor 2B	HTR2B	1	0
G9I2K7	MHC Class I antigen (Fragment)	HLA-B	1	0
Q9H3Y8	Pancreatic progenitor cell differentiation and proliferation factor	PPDPF C20orf149 EXPDF	1	2
I2GAE1	MHC class I antigen (Fragment)	HLA-C	1	0
N0A0Q2	MHC class I antigen (Fragment)	HLA-C	1	0
D6MKV0	MHC class I antigen (Fragment)	HLA-C	1	0
A0A3S6RFI1	MHC class I antigen	HLA-B	1	0
A0A6B7FTW4	MHC class I antigen (Fragment)	HLA-C	1	0
Q540I5	Lactosylceramide 4-alpha-galactosyltransferase	A4GALT	1	0
Q9NXH8	Torsin-4A	TOR4A C9orf167	1	9
Q6IFH4	Olfactory receptor 6B2	OR6B2 OR6B2P	1	0
I0LEY6	MHC class I antigen	HLA-B	1	0
D5M8B8	MHC class I antigen (Fragment)	HLA-C	1	0
Q8NGP9	Olfactory receptor 5AR1	OR5AR1	1	0
Q9C0K3	Actin-related protein 3C	ACTR3C ARP11	1	1
A0A1W1W528	MHC class I antigen	HLA-C	1	0
Q15475	Homeobox protein SIX1	SIX1	1	1
A0A0S4T1S6	MHC class I antigen	HLA-C	1	0
Q8NGM9	Olfactory receptor 8D4	OR8D4	1	0

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