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 **2451 - 2475** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
Q5VT52	Regulation of nuclear pre-mRNA domain-containing protein 2	RPRD2 KIAA0460	Homo sapiens (human)	70	4
Q9H5I5	Piezo-type mechanosensitive ion channel component 2	PIEZO2 C18orf30 C18orf58 FAM38B	Homo sapiens (human)	7	4
Q9Z0E8	Organic cation/carnitine transporter 2	Slc22a5 Octn2	Mus musculus (house mouse)	3	4
Q811D0	Disks large homolog 1	Dlg1 Dlgh1	Mus musculus (house mouse)	3	4
Q7RTX0	Taste receptor type 1 member 3	TAS1R3 T1R3 TR3	Homo sapiens (human)	9	4
Q91X52	L-xylulose reductase	Dcxr	Mus musculus (house mouse)	3	4
Q8N8S7	Protein enabled homolog	ENAH MENA	Homo sapiens (human)	9	4
Q9JHP7	Protein O-glucosyltransferase 2	Poglut2 Ep58 Kdelc1	Mus musculus (house mouse)	3	4
Q8VE88	Protein FAM114A2	Fam114a2	Mus musculus (house mouse)	3	4
Q5H8C1	FRAS1-related extracellular matrix protein 1	FREM1 C9orf143 C9orf145 C9orf154	Homo sapiens (human)	7	4	3p deletion syndrome Angelman syndrome Baraitser-Winter syndrome CAKUT Fraser syndrome 1 Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome NFIA-related disorder Nance-Horan syndrome Potter's syndrome SATB2-associated syndrome Sakati-Nyhan syndrome Smith-Magenis syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome acquired immunodeficiency syndrome anorectal stricture bilateral renal aplasia branchiootic syndrome cardiovascular system disease chromosome 13q14 deletion syndrome chromosome 15q13.3 microdeletion syndrome chromosome 15q24 deletion syndrome chromosome 15q26-qter deletion syndrome chromosome 16p11.2 deletion syndrome, 220-kb chromosome 16p12.2-p11.2 deletion syndrome chromosome 17q12 deletion syndrome chromosome 17q23.1-q23.2 deletion syndrome chromosome 18q deletion syndrome chromosome 1q21.1 deletion syndrome chromosome 1q41-q42 deletion syndrome chromosome 2p16.1-p15 deletion syndrome chromosome 6pter-p24 deletion syndrome chromosome 8q21.11 deletion syndrome chromosome 9p deletion syndrome congenital diaphragmatic hernia craniosynostosis distal 10q deletion syndrome eye disease heart disease hiatus hernia human immunodeficiency virus infectious disease microphthalmia myelofibrosis omphalocele orofaciodigital syndrome I orofaciodigital syndrome X rectal prolapse renal agenesis umbilical hernia
Q9NZN8	CCR4-NOT transcription complex subunit 2	CNOT2 CDC36 NOT2	Homo sapiens (human)	14	4
Q14671	Pumilio homolog 1	PUM1 KIAA0099 PUMH1	Homo sapiens (human)	23	4
P24723	Protein kinase C eta type	PRKCH PKCL PRKCL	Homo sapiens (human)	2	4
Q8BH97	Reticulocalbin-3	Rcn3 D7Ertd671e	Mus musculus (house mouse)	1	4
E9Q4J9	Adhesion G-protein coupled receptor F2	Adgrf2 Gpr111 Pgr20	Mus musculus (house mouse)	6	4
Q8BKX6	Serine/threonine-protein kinase SMG1	Smg1 Atx Kiaa0421 Lip	Mus musculus (house mouse)	4	4
P19221	Prothrombin	F2 Cf2	Mus musculus (house mouse)	4	4
Q8VE98	CD276 antigen	Cd276 B7h3	Mus musculus (house mouse)	4	4
Q6MZW2	Follistatin-related protein 4	FSTL4 KIAA1061	Homo sapiens (human)	8	4
O94910	Adhesion G protein-coupled receptor L1	ADGRL1 KIAA0821 LEC2 LPHN1	Homo sapiens (human)	9	4
Q8IW45	ATP-dependent (S)-NAD(P)H-hydrate dehydratase	NAXD CARKD	Homo sapiens (human)	2	4
Q8NBI5	Equilibrative nucleobase transporter 1	SLC43A3 ENBT1	Homo sapiens (human)	4	4
Q15596	Nuclear receptor coactivator 2	NCOA2 BHLHE75 SRC2 TIF2	Homo sapiens (human)	3	4
P98153	Integral membrane protein DGCR2/IDD	DGCR2 IDD KIAA0163	Homo sapiens (human)	2	4	Bannayan-Riley-Ruvalcaba syndrome Baraitser-Winter syndrome Cowden syndrome DiGeorge syndrome Fraser syndrome Goldenhar syndrome Laron syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Nezelof syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome achondroplasia acromegaly acute myocardial infarction adrenal gland cancer amyloidosis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome bipolar disorder blepharophimosis branchiootic syndrome cancer cervix disease chronic interstitial cystitis congenital heart disease coronary thrombosis craniosynostosis degenerative disc disease delusional disorder diabetes mellitus diabetic ketoacidosis double outlet right ventricle duodenum cancer embryoma epilepsy heart cancer hyperpituitarism hypoparathyroidism-deafness-renal disease syndrome hypoparathyroidism immune system disease intellectual disability interstitial cystitis learning disability microcephaly myocardial infarction myotonic dystrophy type 1 neuroblastoma obsolete type 1 diabetes mellitus 9 orofaciodigital syndrome I orofaciodigital syndrome X osteoporosis paranoid schizophrenia pheochromocytoma primary biliary cholangitis prune belly syndrome pseudohypoparathyroidism schizophrenia silent myocardial infarction small intestine cancer type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus velocardiofacial syndrome ventricular septal defect visual epilepsy
O14976	Cyclin-G-associated kinase	GAK DNAJC26	Homo sapiens (human)	3	4

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