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 **16951 - 16975** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
Q6UXK5	Leucine-rich repeat neuronal protein 1	LRRN1 KIAA1497	Homo sapiens (human)	7	5
Q8WXS8	A disintegrin and metalloproteinase with thrombospondin motifs 14	ADAMTS14	Homo sapiens (human)	7	1
P36268	Inactive glutathione hydrolase 2	GGT2P GGT2	Homo sapiens (human)	7	6
Q6UX72	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 9	B3GNT9	Homo sapiens (human)	7	2	rheumatoid arthritis
O60883	G-protein coupled receptor 37-like 1	GPR37L1 ETBRLP2	Homo sapiens (human)	7	2
P51531	Probable global transcription activator SNF2L2	SMARCA2 BAF190B BRM SNF2A SNF2L2	Homo sapiens (human)	7	2
Q63HN8	E3 ubiquitin-protein ligase RNF213	RNF213 ALO17 C17orf27 KIAA1554 KIAA1618 MYSTR	Homo sapiens (human)	7	3
Q9BXB1	Leucine-rich repeat-containing G-protein coupled receptor 4	LGR4 GPR48	Homo sapiens (human)	7	5
Q9UHF1	Epidermal growth factor-like protein 7	EGFL7 MEGF7	Homo sapiens (human)	7	2
P25116	Proteinase-activated receptor 1	F2R CF2R PAR1 TR	Homo sapiens (human)	7	3
Q99988	Growth/differentiation factor 15	GDF15 MIC1 PDF PLAB PTGFB	Homo sapiens (human)	7	4
P37173	TGF-beta receptor type-2	TGFBR2	Homo sapiens (human)	7	12
Q9UMX0	Ubiquilin-1	UBQLN1 DA41 PLIC1	Homo sapiens (human)	7	1
P14679	Tyrosinase	TYR	Homo sapiens (human)	7	0
P13727	Bone marrow proteoglycan	PRG2 MBP	Homo sapiens (human)	7	6	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 Duchenne muscular dystrophy Ehlers-Danlos syndrome spondylodysplastic type 2 Pick's disease Reye syndrome allergic asthma asthma 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 breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cerebral degeneration cholera colorectal cancer colorectal carcinoma congenital muscular dystrophy dermatophytosis dilated cardiomyopathy 1A dilated cardiomyopathy distal myopathy embryoma endometrial cancer endometrial carcinoma eosinophilic esophagitis facioscapulohumeral muscular dystrophy fungal infectious disease intrinsic asthma large intestine cancer limb-girdle muscular dystrophy lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma muscular dystrophy myelofibrosis myofibrillar myopathy 1 myofibrillar myopathy 3 nodular prostate 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 prostate cancer prostate carcinoma prostatic adenoma rippling muscle disease 2 uterine corpus cancer
O75170	Serine/threonine-protein phosphatase 6 regulatory subunit 2	PPP6R2 KIAA0685 PP6R2 SAPS2	Homo sapiens (human)	7	2
P35443	Thrombospondin-4	THBS4 TSP4	Homo sapiens (human)	7	5
P04180	Phosphatidylcholine-sterol acyltransferase	LCAT	Homo sapiens (human)	7	28	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 Bloom syndrome Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Norum disease Pick's disease Reye syndrome Tangier disease abdominal obesity-metabolic syndrome 1 abetalipoproteinemia acute chest syndrome acute myocardial infarction agenesis of the corpus callosum with peripheral neuropathy anemia aortic atherosclerosis arcus senilis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation blindness brain stem infarction cardiovascular system disease carotid artery disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cholesterol-ester transfer protein deficiency choreaacanthocytosis chronic kidney disease chylomicron retention disease congestive heart failure corneal dystrophy coronary artery disease coronary thrombosis disease of metabolism dry eye syndrome familial combined hyperlipidemia familial hypercholesterolemia familial hyperlipidemia familial lipoprotein lipase deficiency familial nephrotic syndrome gallbladder disease glomerulonephritis granular corneal dystrophy heart disease hemolytic anemia hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hyperalphalipoproteinemia 1 hyperlipoproteinemia type V hypolipoproteinemia inherited metabolic disorder kidney disease kidney failure lipoid nephrosis liver cancer liver disease macrocytic anemia macular corneal dystrophy motor peripheral neuropathy myocardial infarction nephritis nephrosis nephrotic syndrome nutmeg liver obesity obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum ovarian cancer ovarian carcinoma proteinuria pyoureter recurrent corneal erosion renal osteodystrophy rheumatoid arthritis sickle cell anemia silent myocardial infarction steatotic liver disease uremia xerophthalmia
Q9UJU6	Drebrin-like protein	DBNL CMAP SH3P7	Homo sapiens (human)	7	1
P10092	Calcitonin gene-related peptide 2	CALCB CALC2	Homo sapiens (human)	7	1
P27169	Serum paraoxonase/arylesterase 1	PON1 PON	Homo sapiens (human)	7	55
P04792	Heat shock protein beta-1	HSPB1 HSP27 HSP28	Homo sapiens (human)	7	1
Q9Y4B4	Helicase ARIP4	RAD54L2 ARIP4 KIAA0809	Homo sapiens (human)	7	2
Q8TE56	A disintegrin and metalloproteinase with thrombospondin motifs 17	ADAMTS17	Homo sapiens (human)	7	2
Q8TE57	A disintegrin and metalloproteinase with thrombospondin motifs 16	ADAMTS16 KIAA2029	Homo sapiens (human)	7	1

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