GlyCosmos Portal

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

« First

‹ Prev

…

183

184

185

186

187

188

189

190

191

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
P03897	NADH-ubiquinone oxidoreductase chain 3	MT-ND3 MTND3 NADH3 ND3	1	1
Q6VVB1	E3 ubiquitin-protein ligase NHLRC1	NHLRC1 EPM2B	1	1
O43237	Cytoplasmic dynein 1 light intermediate chain 2	DYNC1LI2 DNCLI2 LIC2	1	1
P55211	Caspase-9	CASP9 MCH6	0	1
Q9NWB6	Arginine and glutamate-rich protein 1	ARGLU1	1	1
Q9H6K5	Proline-rich protein 36	PRR36	0	1
P25490	Transcriptional repressor protein YY1	YY1 INO80S	1	1
Q9H160	Inhibitor of growth protein 2	ING2 ING1L	0	1
P31483	Cytotoxic granule associated RNA binding protein TIA1	TIA1	0	1
Q9H944	Mediator of RNA polymerase II transcription subunit 20	MED20 TRFP	0	1
P52306	Rap1 GTPase-GDP dissociation stimulator 1	RAP1GDS1 SMGGDS	1	1
Q9H7P9	Pleckstrin homology domain-containing family G member 2	PLEKHG2	1	1
Q13367	AP-3 complex subunit beta-2	AP3B2	0	1
Q8NGX5	Olfactory receptor 10K1	OR10K1	2	1
Q06455	Protein CBFA2T1	RUNX1T1 AML1T1 CBFA2T1 CDR ETO MTG8 ZMYND2	2	1
O95388	CCN family member 4	CCN4 WISP1	5	1
O75352	Mannose-P-dolichol utilization defect 1 protein	MPDU1	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	1	1
Q9H3T2	Semaphorin-6C	SEMA6C KIAA1869 SEMAY	3	1
Q8TDF5	Neuropilin and tolloid-like protein 1	NETO1 BTCL1	3	1
Q96I59	Asparaginyl-tRNA synthetase	NARS2	1	1
Q00653	Nuclear factor NF-kappa-B p100 subunit	NFKB2 LYT10	3	1
Q96MC4	CEP295 N-terminal-like protein	CEP295NL KIAA1731NL	0	1
Q9H490	Phosphatidylinositol glycan anchor biosynthesis class U protein	PIGU CDC91L1	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	5	1

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

International Collaboration

Acknowledgements