GlyCosmos Portal

Source	Last Updated
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 **9126 - 9150** of **126547** in total

« First

‹ Prev

…

362

363

364

365

366

367

368

369

370

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
F4JA91	Subtilisin-like protease SBT4.5	SBT4.5	Arabidopsis thaliana (thale cress)	7	0
P19801	Diamine oxidase [copper-containing]	AOC1 ABP ABP1 DAO	Homo sapiens (human)	7	77
P49015	Copper-transporting ATPase 1 (Fragment)	ATP7A	Cricetulus griseus (Chinese hamster)	7	0
Q5N7A3	Laccase-6	LAC6	Oryza sativa Japonica Group (Japanese rice)	7	0
Q9LKR7	Beta-glucosidase 24	BGLU24	Arabidopsis thaliana (thale cress)	7	0
Q9LZC5	GDSL esterase/lipase At5g03820	At5g03820	Arabidopsis thaliana (thale cress)	7	0
A0A0S6XH62	ABC-type transporter frbG	frbG	fungal sp. No.11243	7	0
P32781	A-agglutinin-binding subunit	AGA2	Saccharomyces cerevisiae S288C	7	0
Q6UXX5	Inter-alpha-trypsin inhibitor heavy chain H6	ITIH6 ITIH5L	Homo sapiens (human)	7	1
P35858	Insulin-like growth factor-binding protein complex acid labile subunit	IGFALS ALS	Homo sapiens (human)	7	17
Q62645	Glutamate receptor ionotropic, NMDA 2D	Grin2d GluN2D	Rattus norvegicus (Norway rat)	7	0
D2CFS3	Pre-glycoprotein polyprotein GP complex	GPC	Mammarenavirus juninense	7	0
Q207Z6	Hemagglutinin	HA	Influenza A virus (A/turkey/Turkey/1/2005(H5N1))	7	0
P0CO60	Putative lipase ATG15	ATG15	Cryptococcus neoformans var. neoformans JEC21	7	0
Q1ZZM3	Probable rhamnogalacturonase E	rhgE	Aspergillus niger	7	0
F8VQL0	Hepatocyte growth factor receptor	Met	Mus musculus (house mouse)	7	0
Q8NFY4	Semaphorin-6D	SEMA6D KIAA1479	Homo sapiens (human)	7	2
F6V9L3	Angiotensin-converting enzyme	ACE2	Equus caballus (horse)	7	0
Q04695	Keratin, type I cytoskeletal 17	KRT17	Homo sapiens (human)	7	1
Q63HQ2	Pikachurin	EGFLAM AGRINL AGRNL PIKA	Homo sapiens (human)	7	4
Q91WV7	Amino acid transporter heavy chain SLC3A1	Slc3a1 Nbat	Mus musculus (house mouse)	7	14
P17801	Putative receptor protein kinase ZmPK1	PK1	Zea mays	7	0
O60931	Cystinosin	CTNS	Homo sapiens (human)	7	0	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Fanconi anemia Fanconi syndrome Laron syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome achondroplasia androgen insensitivity syndrome anhidrosis 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 bacterial vaginosis bone disease cartilage disease cerebral degeneration cone-rod dystrophy connective tissue disease cystinosis diabetes mellitus diabetic ketoacidosis disease of metabolism distal myopathy eunuchism exocrine pancreatic insufficiency facioscapulohumeral muscular dystrophy fundus albipunctatus glomerulonephritis hypogonadism hypohidrosis hypokalemia hypophosphatemia kidney disease kidney failure limb-girdle muscular dystrophy lysosomal storage disease male infertility muscular dystrophy nephritis nephrolithiasis nephrosis obsolete asthenopia 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 obsolete constipation oculopharyngeal muscular dystrophy osteomalacia premature menopause proteinuria pyoureter recurrent corneal erosion retinal disease retinitis pigmentosa retinitis rickets spondyloepimetaphyseal dysplasia, Sponastrime type uric acid nephrolithiasis vaginitis vulvitis vulvovaginitis
Q9XWL9	Patched-related protein 18	ptr-18	Caenorhabditis elegans	7	0
Q86917	G-protein coupled receptor homolog Q2/3L	Q2/3L	Sheeppox virus KS-1	7	0

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements