GlyCosmos Portal

Displaying entries **12951 - 12975** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
P19404	NADH dehydrogenase [ubiquinone] flavoprotein 2, mitochondrial	NDUFV2	0	1
Q5JS54	Proteasome assembly chaperone 4	PSMG4 C6orf86 PAC4	0	1
Q9NP58	ATP-binding cassette sub-family B member 6	ABCB6 MTABC3 PRP UMAT	1	1
Q6NSI8	SANT and BTB domain regulator of class switch recombination	SANBR KIAA1841	0	1
Q9Y6Y0	Influenza virus NS1A-binding protein	IVNS1ABP ARA3 FLARA3 KIAA0850 KLHL39 NS1 NS1BP	0	1
Q15418	Ribosomal protein S6 kinase alpha-1	RPS6KA1 MAPKAPK1A RSK1	4	1
Q4G163	F-box only protein 43	FBXO43 EMI2	1	1
P28838	Cytosol aminopeptidase	LAP3 LAPEP PEPS	0	1
P55795	Heterogeneous nuclear ribonucleoprotein H2	HNRNPH2 FTP3 HNRPH2	1	1
Q9Y6N1	Cytochrome c oxidase assembly protein COX11, mitochondrial	COX11	1	1
Q9NVH0	Exonuclease 3'-5' domain-containing protein 2	EXD2 C14orf114 EXDL2	0	1
Q15437	Protein transport protein Sec23B	SEC23B	15	1	congenital dyserythropoietic anemia type II congenital dyserythropoietic anemia type III congenital dyserythropoietic anemia type Ib congenital dyserythropoietic anemia
Q9Y4F9	Rho family-interacting cell polarization regulator 2	RIPOR2 C6orf32 DIFF48 FAM65B KIAA0386 PL48	1	1
Q8NCB2	CaM kinase-like vesicle-associated protein	CAMKV	5	1
Q9NWZ5	Uridine-cytidine kinase-like 1	UCKL1 URKL1	0	1
Q96KS0	Prolyl hydroxylase EGLN2	EGLN2 EIT6	0	1
Q13394	Putative nucleotidyltransferase MAB21L1	MAB21L1 CAGR1	2	1
O60260	E3 ubiquitin-protein ligase parkin	PRKN PARK2	0	1
Q9NVJ2	ADP-ribosylation factor-like protein 8B	ARL8B ARL10C GIE1	0	1
Q9BXS6	Nucleolar and spindle-associated protein 1	NUSAP1 ANKT	5	1
O95822	Malonyl-CoA decarboxylase, mitochondrial	MLYCD	1	1	Castleman disease Kaposi's sarcoma Kimura disease Laron syndrome Marfan syndrome Meesmann corneal dystrophy Schmid metaphyseal chondrodysplasia Senior-Loken syndrome achondroplasia acquired immunodeficiency syndrome acute kidney tubular necrosis adult lymphoma autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome cancer cardiomyopathy central nervous system lymphoma childhood lymphoma choline deficiency disease diabetes mellitus diarrhea endomyocardial fibrosis epilepsy essential hypertension familial hypertrophic cardiomyopathy familial nephrotic syndrome focal segmental glomerulosclerosis glomerulonephritis human immunodeficiency virus infectious disease hypertension hypertrophic cardiomyopathy hypoglycemia inherited metabolic disorder kidney disease lactic acidosis lipoid nephrosis liver cirrhosis lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 macular corneal dystrophy membranous glomerulonephritis microphthalmia multicentric Castleman disease nasopharynx carcinoma nephritis nephronophthisis 1 nephronophthisis nephrosclerosis nephrosis nephrotic syndrome normal pressure hydrocephalus obesity obsolete Matthew-Wood syndrome obsolete constipation obsolete ymphosarcoma oral tuberculosis primary immunodeficiency disease pyoureter situs inversus steatotic liver disease systemic Epstein-Barr virus positive T-cell lymphoma of childhood tuberculosis tuberous sclerosis 1 tuberous sclerosis type 2 diabetes mellitus visual epilepsy
Q9NVE4	Coiled-coil domain-containing protein 87	CCDC87	1	1
Q3KQV9	UDP-N-acetylhexosamine pyrophosphorylase-like protein 1	UAP1L1	2	1	hepatocellular carcinoma liver cancer
P30876	DNA-directed RNA polymerase II subunit RPB2	POLR2B	1	1
Q8IV33	Uncharacterized protein KIAA0825	KIAA0825 C5orf36	0	1

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