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 **976 - 1000** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
Q9UK58	Cyclin-L1	CCNL1	Homo sapiens (human)	1
Q9NP66	High mobility group protein 20A	HMG20A HMGX1 HMGXB1	Homo sapiens (human)	1
Q9Y3B9	RRP15-like protein	RRP15 KIAA0507	Homo sapiens (human)	1
Q9UNL4	Inhibitor of growth protein 4	ING4	Homo sapiens (human)	1
P49326	Flavin-containing monooxygenase 5	FMO5	Homo sapiens (human)	1
P0DPB6	DNA-directed RNA polymerases I and III subunit RPAC2	POLR1D	Homo sapiens (human)	1
Q92753	Nuclear receptor ROR-beta	RORB NR1F2 RZRB	Homo sapiens (human)	1
Q96SN8	CDK5 regulatory subunit-associated protein 2	CDK5RAP2 CEP215 KIAA1633	Homo sapiens (human)	1
Q01658	Protein Dr1	DR1	Homo sapiens (human)	1
O95619	YEATS domain-containing protein 4	YEATS4 GAS41	Homo sapiens (human)	1
O14618	Copper chaperone for superoxide dismutase	CCS	Homo sapiens (human)	1
O43752	Syntaxin-6	STX6	Homo sapiens (human)	1
B4DU55	Zinc finger protein 879	ZNF879	Homo sapiens (human)	1
Q9H0P0	Cytosolic 5'-nucleotidase 3A	NT5C3A NT5C3 P5N1 UMPH1	Homo sapiens (human)	1
Q86U06	Probable RNA-binding protein 23	RBM23 RNPC4	Homo sapiens (human)	1
Q6IN85	Serine/threonine-protein phosphatase 4 regulatory subunit 3A	PPP4R3A KIAA2010 PP4R3A SMEK1	Homo sapiens (human)	1
Q7L5Y1	Mitochondrial enolase superfamily member 1	ENOSF1 RTS TYMSAS	Homo sapiens (human)	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	Homo sapiens (human)	1
Q2TAK8	PWWP domain-containing DNA repair factor 3A	PWWP3A EXPAND1 MUM1	Homo sapiens (human)	1
O00506	Serine/threonine-protein kinase 25	STK25 SOK1 YSK1	Homo sapiens (human)	1
P35250	Replication factor C subunit 2	RFC2	Homo sapiens (human)	1
Q9BPY3	Protein FAM118B	FAM118B	Homo sapiens (human)	1
P0C874	Spermatogenesis-associated protein 31D3	SPATA31D3 FAM75D3	Homo sapiens (human)	1
Q6NSZ9	Zinc finger and SCAN domain-containing protein 25	ZSCAN25 ZNF498	Homo sapiens (human)	1
Q9UDY4	DnaJ homolog subfamily B member 4	DNAJB4 DNAJW HLJ1	Homo sapiens (human)	1

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