GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **4026 - 4050** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol ▼	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q6K0P9	Pyrin and HIN domain-containing protein 1	PYHIN1 IFIX	Homo sapiens (human)	0	1
Q9BRQ0	Pygopus homolog 2	PYGO2	Homo sapiens (human)	0	1
P11217	Glycogen phosphorylase, muscle form	PYGM	Homo sapiens (human)	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
P06737	Glycogen phosphorylase, liver form	PYGL	Homo sapiens (human)	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
P11216	Glycogen phosphorylase, brain form	PYGB	Homo sapiens (human)	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
Q53H96	Pyrroline-5-carboxylate reductase 3	PYCR3 PYCRL	Homo sapiens (human)	0	1
Q96C36	Pyrroline-5-carboxylate reductase 2	PYCR2	Homo sapiens (human)	5	2
P32322	Pyrroline-5-carboxylate reductase 1, mitochondrial	PYCR1	Homo sapiens (human)	4	1
Q8TE99	2-phosphoxylose phosphatase 1	PXYLP1 ACPL2 HEL124 XYLP	Homo sapiens (human)	3	2	myopia
Q8NFP0	Peroxisomal testis-specific protein 1	PXT1 STEPP	Homo sapiens (human)	0	1
P49023	Paxillin	PXN	Homo sapiens (human)	5	1
Q9Y6I8	Peroxisomal membrane protein 4	PXMP4 PMP24	Homo sapiens (human)	2	0
Q7Z7A4	PX domain-containing protein kinase-like protein	PXK	Homo sapiens (human)	0	1
A1KZ92	Probable oxidoreductase PXDNL	PXDNL VPO2	Homo sapiens (human)	1	0
Q96GF5	PXDN protein (Fragment)	PXDN	Homo sapiens (human)	1	0
Q92626	Peroxidasin homolog	PXDN KIAA0230 MG50 PRG2 PXD01 VPO VPO1	Homo sapiens (human)	14	51
Q5H9M0	PWWP domain-containing DNA repair factor 3B	PWWP3B MUM1L1	Homo sapiens (human)	1	1
Q2TAK8	PWWP domain-containing DNA repair factor 3A	PWWP3A EXPAND1 MUM1	Homo sapiens (human)	0	1
Q96N64	PWWP domain-containing protein 2A	PWWP2A KIAA1935 MST101	Homo sapiens (human)	1	1
Q15269	Periodic tryptophan protein 2 homolog	PWP2 PWP2H	Homo sapiens (human)	2	1
Q13610	Periodic tryptophan protein 1 homolog	PWP1	Homo sapiens (human)	0	1
Q7Z458	Poliovirus receptor related 2 (Fragment)	PVRL2	Homo sapiens (human)	1	0
Q6SYC2	Poliovirus receptor-related 1 (Fragment)	PVRL1	Homo sapiens (human)	1	0
A0A0A0MSA9	PVR cell adhesion molecule	PVR	Homo sapiens (human)	3	0
A0A0C4DG49	PVR cell adhesion molecule	PVR	Homo sapiens (human)	3	0

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