GlyCosmos Portal

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GlyConnect	April 19, 2023
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GlyGen	June 4, 2024
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Displaying entries **8676 - 8700** 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
P13504	Interleukin-1 receptor type 1	Il1r1 Il-1r1 Il1ra	Mus musculus (house mouse)	7	0
P19699	Hemagglutinin	HA	Influenza A virus (A/equine/Kentucky/2/1986(H3N8))	8	0
M9Z894	Fic domain protein (Fragment)	FICD	Platax orbicularis (orbicular batfish)	1	0
Q8LCW9	Large ribosomal subunit protein P1w	RPP1A	Arabidopsis thaliana (thale cress)	0	1
A0A2K5NNA2	Voltage-dependent L-type calcium channel subunit alpha	CACNA1S	Cercocebus atys (sooty mangabey)	2	0
A1L3I3	Protein FAM171A2	fam171a2	Xenopus laevis (African clawed frog)	3	0
A0A0X8EER5	Matrix protein 2	M2 M	Influenza A virus (A/North Carolina/33/2015(H3N2))	1	0
A0A2R9BA36	Hyaluronidase	HYAL3	Pan paniscus (pygmy chimpanzee)	1	0
A0A0X8ECQ6	Matrix protein 2	M2 M	Influenza A virus (A/Alaska/208/2015(H3N2))	1	0
A0A1X9I535	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
A0A0P7UMV4	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase	Z043_104901	Scleropages formosus (Asian bonytongue)	1	0
A0A2K6A1L6	P2X purinoceptor	P2RX3	Mandrillus leucophaeus (drill)	1	0
Q9TXK1	CUB_2 domain-containing protein	CELE_F54E2.1	Caenorhabditis elegans	2	0
O88273	Gremlin-2	Grem2 Cktsf1b2 Prdc	Mus musculus (house mouse)	2	0
A0A2I2UGF1	Voltage-dependent L-type calcium channel subunit alpha	CACNA1C	Felis catus (domestic cat)	1	0
Q3IAG5	Matrix protein 2	M2 M	Influenza A virus (A/New York/433/2000(H3N2))	1	0
A0A7L3G9K1	Hyaluronidase (Fragment)	Hyal1	Anhinga rufa (African darter)	1	0
Q289N7	Matrix protein 2	M2 M	Influenza A virus (A/Canterbury/36/2000(H1N1))	1	0
C7FGC2	Matrix protein 2	M2 M	Influenza A virus (A/Ohio/04/2008(H3N2))	1	0
Q9CR00	26S proteasome non-ATPase regulatory subunit 9	Psmd9	Mus musculus (house mouse)	1	2
P94111	Protein STRICTOSIDINE SYNTHASE-LIKE 12	SSL12 SS1 SS13	Arabidopsis thaliana (thale cress)	1	0
P32019	Type II inositol 1,4,5-trisphosphate 5-phosphatase	INPP5B OCRL2	Homo sapiens (human)	0	1	Dent disease Duchenne muscular dystrophy Joubert syndrome 1 Joubert syndrome amyotrophic lateral sclerosis autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy congenital hypothyroidism congenital muscular dystrophy distal myopathy facioscapulohumeral muscular dystrophy giant cell glioblastoma glaucoma glioblastoma hypothyroidism limb-girdle muscular dystrophy muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myxedema obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy progressive muscular atrophy rippling muscle disease 2
Q69ZF7	Metal transporter CNNM4	Cnnm4 Acdp4 Kiaa1592	Mus musculus (house mouse)	5	10
A0A3M7E138	SMP-30/Gluconolactonase/LRE-like region domain-containing protein	D0863_05873	Hortaea werneckii	1	0
A0A7L1I130	ATP receptor (Fragment)	P2rx6	Nycticryphes semicollaris	1	0

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