GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
Q9BZL4	Protein phosphatase 1 regulatory subunit 12C	PPP1R12C LENG3 MBS85	1	1
O14618	Copper chaperone for superoxide dismutase	CCS	0	1
Q9HAV0	Guanine nucleotide-binding protein subunit beta-4	GNB4	1	1
Q8IXZ2	Zinc finger CCCH domain-containing protein 3	ZC3H3 KIAA0150 SMICL ZC3HDC3	3	1
O95069	Potassium channel subfamily K member 2	KCNK2 TREK TREK1	4	1
O43752	Syntaxin-6	STX6	0	1
B4DU55	Zinc finger protein 879	ZNF879	0	1
Q8N264	Rho GTPase-activating protein 24	ARHGAP24 FILGAP	1	1
Q9H0P0	Cytosolic 5'-nucleotidase 3A	NT5C3A NT5C3 P5N1 UMPH1	0	1
Q6P0N0	Mis18-binding protein 1	MIS18BP1 C14orf106 KIAA1903 KNL2 M18BP1	1	1
Q86U06	Probable RNA-binding protein 23	RBM23 RNPC4	0	1
P56524	Histone deacetylase 4	HDAC4 KIAA0288	4	1
Q6IN85	Serine/threonine-protein phosphatase 4 regulatory subunit 3A	PPP4R3A KIAA2010 PP4R3A SMEK1	0	1
Q7L5Y1	Mitochondrial enolase superfamily member 1	ENOSF1 RTS TYMSAS	0	1	Down syndrome Hailey-Hailey disease Holt-Oram syndrome Klippel-Trenaunay syndrome Marfan syndrome Plasmodium falciparum malaria Rothmund-Thomson syndrome Rubinstein-Taybi syndrome VACTERL association Werner syndrome adult lymphoma arachnoiditis autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB cancer central nervous system cancer central nervous system lymphoma cerebral malaria childhood leukemia childhood lymphoma colorectal cancer colorectal carcinoma congenital central hypoventilation syndrome cutaneous mastocytosis cutis laxa diffuse cutaneous mastocytosis embryoma endometrial cancer endometrial carcinoma exanthem gliosarcoma hepatitis B herpes zoster high grade glioma intellectual disability large intestine cancer learning disability leukemia lymphoma mal de Meleda malaria mastocytosis meningitis microphthalmia with limb anomalies mixed glioma mixed sleep apnea nail-patella syndrome obsolete ymphosarcoma obstructive sleep apnea ovarian cancer ovarian carcinoma poikiloderma with neutropenia progeria rabies restrictive dermopathy situs inversus sleep apnea split hand-foot malformation 1 with sensorineural hearing loss stomach cancer stomach carcinoma thrombocytopenia-absent radius syndrome tuberous sclerosis urticaria pigmentosa uterine corpus cancer
Q9H479	Fructosamine-3-kinase	FN3K	0	1
P28066	Proteasome subunit alpha type-5	PSMA5	3	1
Q2TAK8	PWWP domain-containing DNA repair factor 3A	PWWP3A EXPAND1 MUM1	0	1
O00506	Serine/threonine-protein kinase 25	STK25 SOK1 YSK1	0	1
Q99758	Phospholipid-transporting ATPase ABCA3	ABCA3 ABC3	6	1
P35250	Replication factor C subunit 2	RFC2	0	1
Q9BPY3	Protein FAM118B	FAM118B	0	1
P0C874	Spermatogenesis-associated protein 31D3	SPATA31D3 FAM75D3	0	1
O43149	Zinc finger ZZ-type and EF-hand domain-containing protein 1	ZZEF1 KIAA0399	2	1
Q2WGJ8	Cation channel sperm-associated auxiliary subunit TMEM249	TMEM249 C8orfK29	1	1
Q6NSZ9	Zinc finger and SCAN domain-containing protein 25	ZSCAN25 ZNF498	0	1

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