GlyCosmos Portal

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GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
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The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **1876 - 1900** 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
P11688	Integrin alpha-5	Itga5	Mus musculus (house mouse)	14	6
Q03137	Ephrin type-A receptor 4	Epha4 Sek Sek1	Mus musculus (house mouse)	5	6
P00735	Prothrombin	F2	Bos taurus (cattle)	3	6
Q9EPR5	VPS10 domain-containing receptor SorCS2	Sorcs2	Mus musculus (house mouse)	9	6
Q3URE9	Leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 2	Lingo2 Lrrn6c	Mus musculus (house mouse)	10	6
Q62469	Integrin alpha-2	Itga2	Mus musculus (house mouse)	9	6
P97333	Neuropilin-1	Nrp1 Nrp	Mus musculus (house mouse)	7	6
Q99J21	Mucolipin-1	Mcoln1 Trpml1	Mus musculus (house mouse)	4	6
Q9EPN1	Neurobeachin	Nbea Lyst2	Mus musculus (house mouse)	21	6
P28654	Decorin	Dcn	Mus musculus (house mouse)	5	6
Q61026	Nuclear receptor coactivator 2	Ncoa2 Grip1 Src2 Tif2	Mus musculus (house mouse)	9	6
Q9H1A3	Protein-L-histidine N-pros-methyltransferase	METTL9 DREV	Homo sapiens (human)	1	6
Q5RJH3	Cadherin-12	Cdh12	Mus musculus (house mouse)	4	6
P70407	Cadherin-9	Cdh9	Mus musculus (house mouse)	6	6
Q9ULT8	E3 ubiquitin-protein ligase HECTD1	HECTD1 KIAA1131	Homo sapiens (human)	26	6
Q6P7S1	Acid ceramidase	Asah1	Rattus norvegicus (Norway rat)	4	6
P55011	Solute carrier family 12 member 2	SLC12A2 NKCC1	Homo sapiens (human)	3	6
Q5VYK3	Proteasome adapter and scaffold protein ECM29	ECPAS ECM29 KIAA0368	Homo sapiens (human)	10	6
P11247	Myeloperoxidase	Mpo	Mus musculus (house mouse)	6	6
P05555	Integrin alpha-M	Itgam	Mus musculus (house mouse)	16	6
Q8C172	Ceramide synthase 6	Cers6 Lass6	Mus musculus (house mouse)	1	6
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
F8VQJ3	Laminin, gamma 1	Lamc1	Mus musculus (house mouse)	14	6
Q3TQ02	Alkaline phosphatase	Alpl Akp2	Mus musculus (house mouse)	3	6
P62847	Small ribosomal subunit protein eS24	RPS24	Homo sapiens (human)	1	6

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