GlyCosmos Portal

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GlyConnect	April 19, 2023
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GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **116626 - 116650** 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
Q9GZN4	Brain-specific serine protease 4	PRSS22 BSSP4 PRSS26	Homo sapiens (human)	1	0
Q9GZN6	Orphan sodium- and chloride-dependent neurotransmitter transporter NTT5	SLC6A16 NTT5	Homo sapiens (human)	1	0
Q9GZN7	Protein rogdi homolog	ROGDI	Homo sapiens (human)	1	1
Q9GZP0	Platelet-derived growth factor D	PDGFD IEGF SCDGFB	Homo sapiens (human)	5	4
Q9GZP4	PITH domain-containing protein 1	PITHD1 C1orf128	Homo sapiens (human)	2	2
Q9GZP7	Vomeronasal type-1 receptor 1	VN1R1 V1RL1 VNR19I1	Homo sapiens (human)	2	0
Q9GZP8	Immortalization up-regulated protein	IMUP C19orf33	Homo sapiens (human)	0	1
Q9GZP9	Derlin-2	DERL2 DER2 FLANA	Homo sapiens (human)	0	1
Q9GZQ4	Neuromedin-U receptor 2	NMUR2 NMU2R TGR1	Homo sapiens (human)	3	0
Q9GZQ6	Neuropeptide FF receptor 1	NPFFR1 GPR147 NPFF1	Homo sapiens (human)	5	0
Q9GZR1	Sentrin-specific protease 6	SENP6 KIAA0797 SSP1 SUSP1	Homo sapiens (human)	2	2
Q9GZR2	RNA exonuclease 4	REXO4 PMC2 XPMC2H	Homo sapiens (human)	0	1
Q9GZR5	Very long chain fatty acid elongase 4	ELOVL4	Homo sapiens (human)	2	6	Kuhnt-Junius degeneration Leber congenital amaurosis Sjogren-Larsson syndrome Stargardt disease achromatopsia acquired color blindness acquired hyperkeratosis acute myocardial infarction age related macular degeneration alternating hemiplegia of childhood angioedema anhidrosis autonomic neuropathy autosomal dominant cerebellar ataxia autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis blindness blue color blindness cancer cardiac arrest central nervous system disease cerebellar ataxia cerebellar disease color blindness cone-rod dystrophy 2 cone-rod dystrophy 7 cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness coronary thrombosis degeneration of macula and posterior pole diabetes mellitus diabetic ketoacidosis dissociated nystagmus dry eye syndrome epilepsy erythrokeratodermia variabilis et progressiva 1 erythrokeratodermia variabilis eye disease fundus albipunctatus glycogen storage disease II granuloma annulare hepatocellular carcinoma hypertropia hypohidrosis ichthyosis inguinal hernia keratosis follicularis liver cancer locked-in syndrome macular degeneration mechanical strabismus mongolian spot myocardial infarction nervous system disease neurodegenerative disease night blindness obsolete congenital ichthyosiform erythroderma ophthalmoplegia pathologic nystagmus pseudoxanthoma elasticum quadriplegia red color blindness red-green color blindness retinitis pigmentosa 25 retinitis pigmentosa 30 retinitis pigmentosa silent myocardial infarction skin disease spinocerebellar ataxia type 34 spontaneous ocular nystagmus strabismus thrombocytopenia type 2 diabetes mellitus urticaria visual epilepsy xerophthalmia
Q9GZR7	ATP-dependent RNA helicase DDX24	DDX24	Homo sapiens (human)	2	1
Q9GZS3	Superkiller complex protein 8	SKIC8 WDR61	Homo sapiens (human)	0	1
Q9GZS9	Carbohydrate sulfotransferase 5	CHST5	Homo sapiens (human)	3	1	adenocarcinoma adenoma cribriform carcinoma granular cell carcinoma tubular adenocarcinoma
Q9GZT3	SRA stem-loop-interacting RNA-binding protein, mitochondrial	SLIRP C14orf156	Homo sapiens (human)	0	1
Q9GZT5	Protein Wnt-10a	WNT10A	Homo sapiens (human)	3	2
Q9GZT9	Egl nine homolog 1	EGLN1 C1orf12	Homo sapiens (human)	0	1
Q9GZU1	Mucolipin-1	MCOLN1 ML4 TRPML1	Homo sapiens (human)	2	3
Q9GZU2	Paternally-expressed gene 3 protein	PEG3 KIAA0287 ZSCAN24	Homo sapiens (human)	1	1
Q9GZU3	Transmembrane protein 39B	TMEM39B	Homo sapiens (human)	1	0
Q9GZU5	Nyctalopin	NYX CLRP	Homo sapiens (human)	6	0	Balo concentric sclerosis Leber congenital amaurosis 1 Stargardt disease achromatopsia 3 achromatopsia acquired color blindness adrenoleukodystrophy blue color blindness central nervous system disease color blindness cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness 1B congenital stationary night blindness 2A congenital stationary night blindness dissociated nystagmus enhanced S-cone syndrome eye disease fundus albipunctatus hypertropia leukemia mechanical strabismus myopia narcolepsy nervous system disease night blindness ophthalmoplegia pathologic nystagmus red color blindness red-green color blindness retinal disease retinitis pigmentosa retinitis spontaneous ocular nystagmus strabismus
Q9GZU7	Carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1	CTDSP1 NIF3 NLIIF SCP1	Homo sapiens (human)	1	1
Q9GZU8	PSME3-interacting protein	PSME3IP1 C16orf94 FAM192A NIP30 PIP30	Homo sapiens (human)	0	1

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