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 **8751 - 8775** 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
Q9VK60	GH25425p	Dmel\CG6180	Drosophila melanogaster (fruit fly)	0	1
A0A5F8MPK9	Phosphatidylinositol-3-phosphatase SAC1	Sacm1l	Mus musculus (house mouse)	0	1
Q62348	Translin	Tsn	Mus musculus (house mouse)	0	1
Q9H7P9	Pleckstrin homology domain-containing family G member 2	PLEKHG2	Homo sapiens (human)	1	1
Q13367	AP-3 complex subunit beta-2	AP3B2	Homo sapiens (human)	0	1
Q8NGX5	Olfactory receptor 10K1	OR10K1	Homo sapiens (human)	2	1
Q06455	Protein CBFA2T1	RUNX1T1 AML1T1 CBFA2T1 CDR ETO MTG8 ZMYND2	Homo sapiens (human)	2	1
V5BEU6	NAD(P)-dependent steroid dehydrogenase protein	TCDM_09280	Trypanosoma cruzi Dm28c	0	1
Q5SWN2	Replication protein A subunit	Rpa1	Mus musculus (house mouse)	0	1
P33306	Protein BCK2	BCK2 CTR7	Saccharomyces cerevisiae S288C	7	1
O09061	Proteasome subunit beta type-1	Psmb1	Mus musculus (house mouse)	2	1
P62897	Cytochrome c, somatic	Cycs	Mus musculus (house mouse)	0	1
O95388	CCN family member 4	CCN4 WISP1	Homo sapiens (human)	5	1
O75352	Mannose-P-dolichol utilization defect 1 protein	MPDU1	Homo sapiens (human)	0	1	IgA glomerulonephritis acquired hyperkeratosis autosomal recessive congenital ichthyosis 1 blindness cancer cerebral degeneration congenital disorder of glycosylation Id congenital disorder of glycosylation If congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital disorder of glycosylation congenital hypothyroidism congenital nystagmus craniosynostosis cystinuria dissociated nystagmus galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hypertropia hypothyroidism ichthyosis keratosis follicularis mechanical strabismus microcephaly mongolian spot myxedema obsolete congenital ichthyosiform erythroderma ophthalmoplegia optic atrophy pathologic nystagmus pseudoxanthoma elasticum spontaneous ocular nystagmus strabismus
Q4DWY3	BRCT domain-containing protein	Tc00.1047053510729.20	Trypanosoma cruzi strain CL Brener	0	1
V5D7S2	Uncharacterized protein	TCDM_08666	Trypanosoma cruzi Dm28c	0	1
Q8N9W8	Golgi-associated RAB2 interactor protein 2	GARIN2 C14orf54 FAM71D	Homo sapiens (human)	1	1
A2BDW0	Tyrosine-protein kinase	Btk	Mus musculus (house mouse)	0	1
Q9H3T2	Semaphorin-6C	SEMA6C KIAA1869 SEMAY	Homo sapiens (human)	3	1
Q8TDF5	Neuropilin and tolloid-like protein 1	NETO1 BTCL1	Homo sapiens (human)	3	1
Q96I59	Asparaginyl-tRNA synthetase	NARS2	Homo sapiens (human)	1	1
Q00653	Nuclear factor NF-kappa-B p100 subunit	NFKB2 LYT10	Homo sapiens (human)	3	1
Q8CI51	PDZ and LIM domain protein 5	Pdlim5 Enh	Mus musculus (house mouse)	11	1
Q96MC4	CEP295 N-terminal-like protein	CEP295NL KIAA1731NL	Homo sapiens (human)	0	1
Q9H490	Phosphatidylinositol glycan anchor biosynthesis class U protein	PIGU CDC91L1	Homo sapiens (human)	0	1	bladder carcinoma breast cancer breast carcinoma cancer carcinoma cerebral degeneration colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma differentiated thyroid gland carcinoma dysplastic nevus syndrome embryoma epilepsy hepatocellular carcinoma intellectual disability large intestine cancer learning disability liver cancer melanoma nasopharynx carcinoma papillary carcinoma sarcomatoid carcinoma scoliosis skin benign neoplasm skin cancer skin melanoma urinary bladder cancer visual epilepsy

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