GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
Q00005	Serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B beta isoform	PPP2R2B	0	1
P13942	Collagen alpha-2(XI) chain	COL11A2	3	1
Q86W50	RNA N6-adenosine-methyltransferase METTL16	METTL16 METT10D	0	1
O94986	Centrosomal protein of 152 kDa	CEP152 KIAA0912	3	1
Q15050	Ribosome biogenesis regulatory protein homolog	RRS1 KIAA0112 RRR	3	1
Q969Q0	Ribosomal protein eL42-like	RPL36AL	0	1
Q9Y2D2	UDP-N-acetylglucosamine transporter	SLC35A3	0	1	Marfan syndrome autism spectrum disorder autistic disorder central nervous system cancer congenital disorder of glycosylation epilepsy gliosarcoma high grade glioma intellectual disability learning disability microcephaly mixed glioma mucopolysaccharidosis IV multiple epiphyseal dysplasia osteochondrodysplasia scoliosis situs inversus spondylocostal dysostosis syndromic X-linked intellectual disability 94 tuberous sclerosis visual epilepsy
Q15697	Zinc finger protein 174	ZNF174 ZSCAN8	0	1
Q9H0E7	Ubiquitin carboxyl-terminal hydrolase 44	USP44	0	1
O60306	RNA helicase aquarius	AQR KIAA0560	2	1
P49753	Acyl-coenzyme A thioesterase 2, mitochondrial	ACOT2 PTE2 PTE2A	0	1	coronary artery disease diabetes mellitus type 2 diabetes mellitus
P14678	Small nuclear ribonucleoprotein-associated proteins B and B'	SNRPB COD SNRPB1	1	1
Q4G176	Malonate--CoA ligase ACSF3, mitochondrial	ACSF3	1	1	B-cell lymphoma adult lymphoma amnestic disorder brain disease central nervous system lymphoma childhood lymphoma combined malonic and methylmalonic acidemia diarrhea disease of metabolism dystonia hypoglycemia inherited metabolic disorder lymphoma methylmalonic acidemia microcephaly migraine obsolete ymphosarcoma retrograde amnesia
Q05193	Dynamin-1	DNM1 DNM	1	1
O60765	Zinc finger protein 354A	ZNF354A EZNF HKL1 TCF17	0	1
A0A087WWU8	Tropomyosin 3	TPM3	0	1
Q8N616	Putative uncharacterized protein encoded by LINC00311	LINC00311 NCRNA00311 TMEM148	0	1
Q8TCT1	Phosphoethanolamine/phosphocholine phosphatase	PHOSPHO1	0	1	diabetes mellitus osteomalacia rickets type 2 diabetes mellitus
Q32P51	Heterogeneous nuclear ribonucleoprotein A1-like 2	HNRNPA1L2 HNRNPA1L	2	1
P35227	Polycomb group RING finger protein 2	PCGF2 MEL18 RNF110 ZNF144	1	1
P49765	Vascular endothelial growth factor B	VEGFB VRF	1	1
O60701	UDP-glucose 6-dehydrogenase	UGDH	1	1	Graves' disease Laron syndrome Zollinger-Ellison syndrome achondroplasia beta thalassemia breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cholangiocarcinoma diarrhea enophthalmos giant cell glioblastoma giardiasis glioblastoma hepatocellular carcinoma high grade glioma hyperinsulinism hyperthyroidism hypoglycemia intrahepatic cholangiocarcinoma liver cancer lung benign neoplasm lung cancer lung carcinoma obsolete exophthalmos orbital disease peripheral artery disease placental insufficiency primary hyperoxaluria thalassemia thyrotoxicosis
O15055	Period circadian protein homolog 2	PER2 KIAA0347	10	1
Q96EF0	Myotubularin-related protein 8	MTMR8	1	1	breast cancer
P09067	Homeobox protein Hox-B5	HOXB5 HOX2A	1	1

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