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 **6001 - 6025** 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
Q8LPT1	ABC transporter B family member 6	ABCB6 MDR6 PGP6	Arabidopsis thaliana (thale cress)	8	0
A0A673IZH8	Fibroblast growth factor receptor	LOC107724577	Sinocyclocheilus rhinocerous	8	0
B3LZ39	Glutamate [NMDA] receptor subunit 1	Nmdar1	Drosophila ananassae	8	0
A0A7L2S781	Fibroblast growth factor receptor 2 (Fragment)	Fgfr2	Mystacornis crossleyi	8	0
A0A7K7TW42	Fibroblast growth factor receptor 1 (Fragment)	Fgfr1	Ibidorhyncha struthersii	8	0
Q9Z2G6	Protein sel-1 homolog 1	Sel1l Sel1h	Mus musculus (house mouse)	8	9
Q29451	Lysosomal alpha-mannosidase	MAN2B1 MANB	Bos taurus (cattle)	8	0
A0A7L3R010	Fibroblast growth factor receptor 1 (Fragment)	Fgfr1	Cettia cetti	8	0
Q12789	General transcription factor 3C polypeptide 1	GTF3C1	Homo sapiens (human)	8	4
A0A8B7V5X2	Fibroblast growth factor receptor	Fgfr2	Castor canadensis (American beaver)	8	0
O76061	Stanniocalcin-2	STC2	Homo sapiens (human)	8	6
A0A7L0ZUA2	Fibroblast growth factor receptor 2 (Fragment)	Fgfr2	Oxyruncus cristatus (sharpbill)	8	0
B3NS99	Tyrosine-protein kinase-like otk	otk	Drosophila erecta	8	0
A0A7L0JZ20	Fibroblast growth factor receptor 2 (Fragment)	Fgfr2	Chauna torquata (southern screamer)	8	0
A0A2R9B1F3	Fibroblast growth factor receptor	FGFR2	Pan paniscus (pygmy chimpanzee)	8	0
A0A2K6GVQ0	Fibroblast growth factor receptor	FGFR2	Propithecus coquereli (Coquerel's sifaka)	8	0
A0A8B8TXI0	Fibroblast growth factor receptor	FGFR2	Camelus ferus (Wild Bactrian camel)	8	0
A0A6D2XXZ6	Fibroblast growth factor receptor	fgfr2	Takifugu rubripes (torafugu)	8	0
A0A2K5WIM5	Fibroblast growth factor receptor	FGFR1	Macaca fascicularis (crab-eating macaque)	8	0
A0A0A6YXN8	Signal-regulatory protein beta 1B	Sirpb1b	Mus musculus (house mouse)	8	3
Q8JFR5	Mast/stem cell growth factor receptor kita	kita kit sparse	Danio rerio (zebrafish)	8	0
Q5VV63	Attractin-like protein 1	ATRNL1 KIAA0534	Homo sapiens (human)	8	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 B-cell lymphoma Becker muscular dystrophy Bloom syndrome Duchenne muscular dystrophy Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Langerhans-cell histiocytosis Laron syndrome Marfan syndrome Pick's disease Reye syndrome Sjogren's syndrome Wilson disease achondroplasia acromegaly acute myeloid leukemia adult hypophosphatasia allergic asthma amyotrophic lateral sclerosis ankylosing spondylitis asthma 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 bone cancer bone disease bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer cardiovascular system disease cartilage disease cerebral degeneration cerebral palsy childhood osteosarcoma cholestasis choriocarcinoma chromophobe renal cell carcinoma chromosome 17p13.1 deletion syndrome clear cell renal cell carcinoma cleft palate collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer connective tissue disease craniosynostosis diabetes mellitus distal arthrogryposis distal myopathy embryonal cancer endomyocardial fibrosis esophagitis extrahepatic cholestasis facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy familial hyperlipidemia familial hypocalciuric hypercalcemia 1 gallbladder disease gastroesophageal reflux disease germ cell and embryonal cancer germ cell cancer germinoma goiter heart disease hematopoietic system disease hemiplegia hemochromatosis hepatitis C hepatitis hepatocellular carcinoma hereditary elliptocytosis hypercalcemia hyperpituitarism hypogonadism hypophosphatasia infantile hypophosphatasia inflammatory liposarcoma iron metabolism disease isolated cleft palate keratoconjunctivitis sicca kidney failure large intestine cancer limb-girdle muscular dystrophy lipoma lissencephaly liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma muscular dystrophy myeloproliferative disorder with eosinophilia myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 nephrocalcinosis nephrolithiasis neurodegenerative disease non-Hodgkin lymphoma nonpapillary renal cell carcinoma nontoxic goiter 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 obsolete ymphosarcoma oculopharyngeal muscular dystrophy osteoporosis osteosarcoma papillary renal cell carcinoma peptic esophagitis phosphorus metabolism disease placenta cancer pleomorphic lipoma primary biliary cholangitis primary hyperparathyroidism progressive muscular atrophy prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma reticulosarcoma rheumatoid arthritis sarcomatoid renal cell carcinoma sclerosing liposarcoma situs inversus spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy steatotic liver disease subcortical band heterotopia thyroid gland disease tuberous sclerosis type 2 diabetes mellitus uremia uric acid nephrolithiasis vitelliform macular dystrophy well-differentiated liposarcoma
A0A7L4I2D7	Fibroblast growth factor receptor 2 (Fragment)	Fgfr2	Scopus umbretta (hamerkop)	8	0
A0A6P3RAC5	Fibroblast growth factor receptor	FGFR1	Pteropus vampyrus (large flying fox)	8	0
L5KB29	Fibroblast growth factor receptor	PAL_GLEAN10021565	Pteropus alecto (black flying fox)	8	0

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