GlyCosmos Portal

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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 **15951 - 15975** 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
Q9Y5X5	Neuropeptide FF receptor 2	NPFFR2 GPR74 NPFF2 NPGPR	Homo sapiens (human)	4	0
P56747	Claudin-6	CLDN6	Homo sapiens (human)	4	1
P46940	Ras GTPase-activating-like protein IQGAP1	IQGAP1 KIAA0051	Homo sapiens (human)	4	4
Q99880	Histone H2B type 1-L	H2BC13 H2BFC HIST1H2BL	Homo sapiens (human)	4	1
Q13523	Serine/threonine-protein kinase PRP4 homolog	PRP4K KIAA0536 PRP4 PRP4B PRP4H PRPF4K	Homo sapiens (human)	4	2
Q12999	Tetraspanin-31	TSPAN31 SAS	Homo sapiens (human)	4	0
Q9P1Y6	PHD and RING finger domain-containing protein 1	PHRF1 KIAA1542	Homo sapiens (human)	4	2
B4DS77	Protein shisa-9	SHISA9	Homo sapiens (human)	4	2
Q14439	G-protein coupled receptor 176	GPR176	Homo sapiens (human)	4	0
Q96N87	Inactive sodium-dependent neutral amino acid transporter B(0)AT3	SLC6A18 B0AT3 XTRP2	Homo sapiens (human)	4	0
P09172	Dopamine beta-hydroxylase	DBH	Homo sapiens (human)	4	12
B4DHZ6	Transferrin, isoform CRA_c	TF	Homo sapiens (human)	4	0
O00429	Dynamin-1-like protein	DNM1L DLP1 DRP1	Homo sapiens (human)	4	1
Q96DF8	Splicing factor ESS-2 homolog	ESS2 DGCR13 DGCR14 DGSH DGSI ES2	Homo sapiens (human)	4	2
Q75T13	GPI inositol-deacylase	PGAP1	Homo sapiens (human)	4	6	Burkitt lymphoma Laron syndrome achondroplasia agnosia autosomal recessive intellectual developmental disorder brain disease cerebral degeneration choreatic disease congenital disorder of glycosylation depressive disorder developmental coordination disorder dysthymic disorder dystonia epilepsy factor XII deficiency focal epilepsy fundus dystrophy holoprosencephaly 1 holoprosencephaly intellectual disability learning disability lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia paroxysmal nocturnal hemoglobinuria partial motor epilepsy stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 visual epilepsy
Q9UQP3	Tenascin-N	TNN TNW	Homo sapiens (human)	4	15
V9HWF6	Alpha-1-acid glycoprotein	HEL-S-153w	Homo sapiens (human)	4	0
Q9Y661	Heparan sulfate glucosamine 3-O-sulfotransferase 4	HS3ST4 3OST4	Homo sapiens (human)	4	0	acute lymphoblastic leukemia age related macular degeneration amphetamine abuse degeneration of macula and posterior pole lymphoblastic lymphoma macular degeneration
P25789	Proteasome subunit alpha type-4	PSMA4 HC9 PSC9	Homo sapiens (human)	4	1
Q9C002	Normal mucosa of esophagus-specific gene 1 protein	NMES1 C15orf48	Homo sapiens (human)	4	1
O76096	Cystatin-F	CST7	Homo sapiens (human)	4	2
Q9UHG2	ProSAAS	PCSK1N	Homo sapiens (human)	4	4
Q96J65	ATP-binding cassette sub-family C member 12	ABCC12 MRP9	Homo sapiens (human)	4	0
Q9UBU7	Protein DBF4 homolog A	DBF4 ASK DBF4A ZDBF1	Homo sapiens (human)	4	1
Q9Y5H9	Protocadherin alpha-2	PCDHA2	Homo sapiens (human)	4	0

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