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 **4651 - 4675** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
P03897	NADH-ubiquinone oxidoreductase chain 3	MT-ND3 MTND3 NADH3 ND3	Homo sapiens (human)	1	1
Q6VVB1	E3 ubiquitin-protein ligase NHLRC1	NHLRC1 EPM2B	Homo sapiens (human)	1	1
O43237	Cytoplasmic dynein 1 light intermediate chain 2	DYNC1LI2 DNCLI2 LIC2	Homo sapiens (human)	1	1
P55211	Caspase-9	CASP9 MCH6	Homo sapiens (human)	0	1
Q9NWB6	Arginine and glutamate-rich protein 1	ARGLU1	Homo sapiens (human)	1	1
Q9H6K5	Proline-rich protein 36	PRR36	Homo sapiens (human)	0	1
P25490	Transcriptional repressor protein YY1	YY1 INO80S	Homo sapiens (human)	1	1
Q9H160	Inhibitor of growth protein 2	ING2 ING1L	Homo sapiens (human)	0	1
P31483	Cytotoxic granule associated RNA binding protein TIA1	TIA1	Homo sapiens (human)	0	1
Q9H944	Mediator of RNA polymerase II transcription subunit 20	MED20 TRFP	Homo sapiens (human)	0	1
P52306	Rap1 GTPase-GDP dissociation stimulator 1	RAP1GDS1 SMGGDS	Homo sapiens (human)	1	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
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
Q8N9W8	Golgi-associated RAB2 interactor protein 2	GARIN2 C14orf54 FAM71D	Homo sapiens (human)	1	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
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
Q8NCW0	Kremen protein 2	KREMEN2 KRM2	Homo sapiens (human)	5	1

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