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 **8051 - 8075** 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
P61562	Syncytin-1	ERVW-1 ERVWE1	Hylobates pileatus (pileated gibbon)	7	0
A4RF05	Vacuolar protein sorting/targeting protein 10	VPS10	Pyricularia oryzae 70-15	7	0
Q95228	Kappa-casein (Fragment)	CSN3 CSN10 CSNK	Odocoileus virginianus virginianus (Virginia white-tailed deer)	7	0
Q9W0R5	Probable G-protein coupled receptor Mth-like 10	mthl10 mth2	Drosophila melanogaster (fruit fly)	7	0
P25705	ATP synthase subunit alpha, mitochondrial	ATP5F1A ATP5A ATP5A1 ATP5AL2 ATPM	Homo sapiens (human)	7	1
P26096	Hemagglutinin	HA	Influenza A virus (A/equine/C.Detroit/1/64(H7N7))	7	0
Q13469	Nuclear factor of activated T-cells, cytoplasmic 2	NFATC2 NFAT1 NFATP	Homo sapiens (human)	7	2
Q6FQN3	ABC multidrug transporter SNQ2	SNQ2	Nakaseomyces glabratus CBS 138	7	0
Q61576	Peptidyl-prolyl cis-trans isomerase FKBP10	Fkbp10 Fkbp-rs Fkbp1-rs Fkbp6 Fkbp65 Fkbprp	Mus musculus (house mouse)	7	6
Q9NAS9	CLIP domain-containing serine protease B15	CLIPB15 ser3	Anopheles gambiae (African malaria mosquito)	7	0
Q61292	Laminin subunit beta-2	Lamb2 Lams	Mus musculus (house mouse)	7	11
Q5PRE5	Proline and serine-rich protein 1	Proser1	Mus musculus (house mouse)	7	1
B2KSC5	Pre-glycoprotein polyprotein GP complex	GPC	North American arenavirus	7	0
O00443	Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha	PIK3C2A	Homo sapiens (human)	7	1	Duchenne muscular dystrophy Gamstorp-Wohlfart syndrome Kaposi's sarcoma Laron syndrome Norum disease Tangier disease Unverricht-Lundborg syndrome abetalipoproteinemia achondroplasia acquired immunodeficiency syndrome acute myocardial infarction anodontia arteriosclerotic cardiovascular disease atherosclerosis atypical chronic myeloid leukemia, BCR-ABL1 negative 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 blepharospasm breast cancer breast carcinoma cancer choreaacanthocytosis chronic monocytic leukemia congenital hypothyroidism congenital muscular dystrophy coronary artery disease coronary thrombosis cryptorchidism diabetes mellitus disease of mental health distal myopathy early myoclonic encephalopathy embryoma episodic ataxia type 1 facioscapulohumeral muscular dystrophy familial periodic paralysis fibromyalgia focal hand dystonia gastrointestinal stromal tumor glaucoma hypercalcemia hyperphosphatemia hypolipoproteinemia hypothyroidism leukopenia limb-girdle muscular dystrophy lymphoid leukemia muscular dystrophy myeloid leukemia myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myositis myotonic dystrophy type 2 myxedema nephrocalcinosis neuroleptic malignant syndrome nutmeg liver 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 phosphorus metabolism disease placental insufficiency protein-losing enteropathy psychotic disorder rippling muscle disease 2 schizoaffective disorder schizophrenia schizophreniform disorder scoliosis sensorineural hearing loss silent myocardial infarction systemic lupus erythematosus thrombocytopenia tibial muscular dystrophy tooth agenesis type 2 diabetes mellitus
A0PJK7	Cadherin-related family member 5	Cdhr5 Mupcdh	Mus musculus (house mouse)	7	0
Q00968	Pro-epidermal growth factor	EGF	Sus scrofa (pig)	7	0
Q05D42	Cdcp1 protein (Fragment)	Cdcp1	Mus musculus (house mouse)	7	0
A2QAS2	Probable mannosyl-oligosaccharide alpha-1,2-mannosidase 1B	mns1B msdS	Aspergillus niger CBS 513.88	7	0
P33306	Protein BCK2	BCK2 CTR7	Saccharomyces cerevisiae S288C	7	1
Q02809	Procollagen-lysine,2-oxoglutarate 5-dioxygenase 1	PLOD1 LLH PLOD	Homo sapiens (human)	7	57	Ehlers-Danlos syndrome kyphoscoliotic type 1 brittle cornea syndrome 1
A0A2K6K3H4	Angiotensin-converting enzyme	ACE	Rhinopithecus bieti (black snub-nosed monkey)	7	0
C4R628	Vacuolar membrane protease	PAS_chr3_0953	Komagataella phaffii GS115	7	0
Q751Z0	Plasma membrane fusion protein PRM1	PRM1	Eremothecium gossypii ATCC 10895	7	0
Q6Z8L2	Putative laccase-9	LAC9	Oryza sativa Japonica Group (Japanese rice)	7	0
P17697	Clusterin	CLU	Bos taurus (cattle)	7	0

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