GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol ▲	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q13610	Periodic tryptophan protein 1 homolog	PWP1	0	1
Q15269	Periodic tryptophan protein 2 homolog	PWP2 PWP2H	2	1
Q96N64	PWWP domain-containing protein 2A	PWWP2A KIAA1935 MST101	1	1
Q2TAK8	PWWP domain-containing DNA repair factor 3A	PWWP3A EXPAND1 MUM1	0	1
Q5H9M0	PWWP domain-containing DNA repair factor 3B	PWWP3B MUM1L1	1	1
Q92626	Peroxidasin homolog	PXDN KIAA0230 MG50 PRG2 PXD01 VPO VPO1	14	51
Q96GF5	PXDN protein (Fragment)	PXDN	1	0
A1KZ92	Probable oxidoreductase PXDNL	PXDNL VPO2	1	0
Q7Z7A4	PX domain-containing protein kinase-like protein	PXK	0	1
Q9Y6I8	Peroxisomal membrane protein 4	PXMP4 PMP24	2	0
P49023	Paxillin	PXN	5	1
Q8NFP0	Peroxisomal testis-specific protein 1	PXT1 STEPP	0	1
Q8TE99	2-phosphoxylose phosphatase 1	PXYLP1 ACPL2 HEL124 XYLP	3	2	myopia
P32322	Pyrroline-5-carboxylate reductase 1, mitochondrial	PYCR1	4	1
Q96C36	Pyrroline-5-carboxylate reductase 2	PYCR2	5	2
Q53H96	Pyrroline-5-carboxylate reductase 3	PYCR3 PYCRL	0	1
P11216	Glycogen phosphorylase, brain form	PYGB	2	3	acute myocardial infarction adenoid cystic carcinoma breast cancer cancer coronary artery disease coronary thrombosis diabetes mellitus embryoma lung cancer lung non-small cell carcinoma myocardial infarction salivary gland adenoid cystic carcinoma salivary gland cancer silent myocardial infarction type 2 diabetes mellitus
P06737	Glycogen phosphorylase, liver form	PYGL	3	3	Gerstmann-Straussler-Scheinker syndrome Gorham's disease Laron syndrome achondroplasia cystinuria galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease III glycogen storage disease IV glycogen storage disease Ia glycogen storage disease V glycogen storage disease VI glycogen storage disease VII glycogen storage disease hepatocellular carcinoma hypoglycemia liver cancer
P11217	Glycogen phosphorylase, muscle form	PYGM	0	1	Gerstmann-Straussler-Scheinker syndrome Gorham's disease Peutz-Jeghers syndrome X-linked myopathy with excessive autophagy 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 bacterial sepsis breast cancer breast carcinoma cancer carcinoma cholestasis coronary artery disease cystinuria disease of metabolism distal myopathy facioscapulohumeral muscular dystrophy familial adenomatous polyposis familial periodic paralysis galactosemia gastrinoma glucosephosphate dehydrogenase deficiency glycogen storage disease IV glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease V glycogen storage disease VI glycogen storage disease VII glycogen storage disease gout head and neck squamous cell carcinoma insulinoma invasive lobular carcinoma islet cell tumor isolated elevated serum creatine phosphokinase levels kidney failure limb-girdle muscular dystrophy lipoma melanoma multiple endocrine neoplasia type 1 multiple symmetric lipomatosis muscular dystrophy myoglobinuria myopathy 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 pleomorphic lipoma pre-eclampsia pseudosarcomatous fibromatosis sarcomatoid carcinoma skin melanoma vitelliform macular dystrophy von Hippel-Lindau disease
Q9BRQ0	Pygopus homolog 2	PYGO2	0	1
Q6K0P9	Pyrin and HIN domain-containing protein 1	PYHIN1 IFIX	0	1
Q8N2H3	Pyridine nucleotide-disulfide oxidoreductase domain-containing protein 2	PYROXD2 C10orf33	1	1
P20742	Pregnancy zone protein	PZP CPAMD6	10	8
P47897	Glutamine--tRNA ligase	QARS1 QARS	2	2
Q96PU8	KH domain-containing RNA-binding protein QKI	QKI HKQ	4	3

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