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 **9526 - 9550** 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
P0DN87	Choriogonadotropin subunit beta 7	CGB7	Homo sapiens (human)	6	0
O00451	GDNF family receptor alpha-2	GFRA2 GDNFRB RETL2 TRNR2	Homo sapiens (human)	6	6	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Hirschsprung's disease adenocarcinoma adenoma bipolar disorder cancer colorectal cancer colorectal carcinoma follicular adenoma frontotemporal dementia hepatocellular carcinoma large intestine cancer lingual-facial-buccal dyskinesia liver cancer microcystic adenoma neuroblastoma neuropathy pancreatic cancer pancreatic carcinoma papillary adenoma peripheral nervous system disease polyneuropathy preretinal fibrosis schizophrenia secondary Parkinson disease
Q9H6E4	Coiled-coil domain-containing protein 134	CCDC134	Homo sapiens (human)	6	2
A0A0F7IQ06	Alpha v integrin	Itgav	Mus musculus (house mouse)	6	0
Q07837	Amino acid transporter heavy chain SLC3A1	SLC3A1 NBAT	Homo sapiens (human)	6	37	IgA glomerulonephritis Marfan syndrome abdominal obesity-metabolic syndrome 1 acute myocardial infarction 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 breast cancer breast carcinoma bulimia nervosa calcinosis calcium metabolism disease cancer chronic kidney disease colon carcinoma colorectal cancer congenital myasthenic syndrome 22 congenital ptosis coronary thrombosis cystinuria diabetes mellitus diabetic ketoacidosis distal myopathy epilepsy essential hypertension facioscapulohumeral muscular dystrophy galactosemia giant cell glioblastoma glioblastoma glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease high grade glioma hypercalcemia hypertension hypoglycemia hypogonadism hypotonia-cystinuria syndrome interstitial nephritis kidney failure lactic acidosis limb-girdle muscular dystrophy muscular dystrophy myocardial infarction nephrocalcinosis nephrolithiasis nephrosclerosis 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 panic disorder phosphorus metabolism disease primary pulmonary hypertension prostate cancer prostate carcinoma ptosis pyelitis pyelonephritis renal hypertension renal infectious disease silent myocardial infarction situs inversus synovial sarcoma tuberous sclerosis type 2 diabetes mellitus uric acid nephrolithiasis urinary tract obstruction vesicoureteral reflux visual epilepsy
Q9NIV1	Eukaryotic translation initiation factor 2-alpha kinase	PEK EIF2AK3	Drosophila melanogaster (fruit fly)	6	0
Q5QQ52	Xylosyltransferase sqv-6	sqv-6 xt	Caenorhabditis briggsae	6	0
D4APE3	Subtilisin-like protease 11	SUB11	Trichophyton benhamiae CBS 112371	6	0
P97855	Ras GTPase-activating protein-binding protein 1	G3bp1 G3bp	Mus musculus (house mouse)	6	3
P05543	Thyroxine-binding globulin	SERPINA7 TBG	Homo sapiens (human)	6	41
Q8N5C8	TGF-beta-activated kinase 1 and MAP3K7-binding protein 3	TAB3 MAP3K7IP3	Homo sapiens (human)	6	1
P16220	Cyclic AMP-responsive element-binding protein 1	CREB1	Homo sapiens (human)	6	3
Q8HZK2	Dual oxidase 2	DUOX2	Sus scrofa (pig)	6	0
O62855	Deoxyribonuclease-2-alpha	DNASE2 DNASE2A DNL2	Sus scrofa (pig)	6	0
C0SJ49	Leucine aminopeptidase 1	LAP1	Paracoccidioides brasiliensis Pb03	6	0
Q15059	Bromodomain-containing protein 3	BRD3 KIAA0043 RING3L	Homo sapiens (human)	6	1
Q553W9	Ceroid-lipofuscinosis neuronal protein 5 homolog	cln5	Dictyostelium discoideum	6	0
Q8SPY6	Non-secretory ribonuclease	RNASE2 EDN RNS2	Chlorocebus aethiops (grivet)	6	0
Q6K4T4	LRR receptor kinase SERK2	SERK4	Oryza sativa Japonica Group (Japanese rice)	6	0
Q3UFS5	Phospholipid transfer protein	Pltp	Mus musculus (house mouse)	6	0
Q9ULB1	Neurexin-1	NRXN1 KIAA0578	Homo sapiens (human)	6	6
Q5UQP0	Uncharacterized protein L448	MIMI_L448	Acanthamoeba polyphaga mimivirus	6	0
Q3UKC6	receptor protein-tyrosine kinase	Csf1r	Mus musculus (house mouse)	6	0
A6ZRQ9	Topoisomerase I damage affected protein 7	TDA7	Saccharomyces cerevisiae YJM789	6	0
Q9GYL2	Metal transporter cnnm-2	cnnm-2	Caenorhabditis elegans	6	0

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