GlyCosmos Portal

Displaying entries **16576 - 16600** of **16604** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
P04275	von Willebrand factor	F8VWF VWF	30	203	Behcet's disease Bernard-Soulier syndrome atrial fibrillation end stage renal disease essential thrombocythemia pulmonary hypertension von Willebrand's disease 1 von Willebrand's disease 2 von Willebrand's disease 3 von Willebrand's disease
P01857	Immunoglobulin heavy constant gamma 1	IGHG1	2	207
Q14956	Transmembrane glycoprotein NMB	GPNMB HGFIN NMB UNQ1725/PRO9925	14	208	primary localized cutaneous amyloidosis 3
P01588	Erythropoietin	EPO	4	209	Alzheimer's disease Parkinson's disease acute kidney failure congestive heart failure diabetic angiopathy diabetic neuropathy diabetic retinopathy familial erythrocytosis 5 glaucoma high grade glioma limb ischemia middle cerebral artery infarction myocardial infarction nephrotic syndrome neurodegenerative disease placental insufficiency porphyria pulmonary hypertension transient cerebral ischemia
P05090	Apolipoprotein D	APOD	3	215	obesity type 2 diabetes mellitus
P05556	Integrin beta-1	FNRB ITGB1 MDF2 MSK12	27	215
P07996	Thrombospondin-1	THBS1 TSP TSP1	24	216	cholangiocarcinoma pancreatic cancer pancreatic ductal carcinoma primary open angle glaucoma
P01876	Immunoglobulin heavy constant alpha 1	IGHA1	14	217
Q08380	Galectin-3-binding protein	LGALS3BP M2BP	14	220
P41222	Prostaglandin-H2 D-isomerase	PDS PTGDS	8	221	carotid artery disease
P13987	CD59 glycoprotein	CD59 MIC11 MIN1 MIN2 MIN3 MSK21	9	224	colorectal carcinoma ovarian cancer
P00450	Ceruloplasmin	CP	15	228	aceruloplasminemia epilepsy hemosiderosis
P02790	Hemopexin	HPX	11	235
P01871	Immunoglobulin heavy constant mu	IGHM	9	237
P02763	Alpha-1-acid glycoprotein 1	AGP1 ORM1	5	238
P02788	Lactotransferrin	GIG12 LF LTF	5	252	candidiasis lung non-small cell carcinoma renal cell carcinoma
P01009	Alpha-1-antitrypsin	AAT PI PRO0684 PRO2209 SERPINA1	10	266	alpha 1-antitrypsin deficiency arteriosclerosis chemical colitis chronic obstructive pulmonary disease human immunodeficiency virus infectious disease ileitis liver cirrhosis liver disease pulmonary emphysema
P02751	Fibronectin	FN FN1	40	272	calcium oxalate nephrolithiasis membranoproliferative glomerulonephritis spondylometaphyseal dysplasia corner fracture type
P21810	Biglycan	BGN SLRR1A	8	274	Meester-Loeys syndrome X-linked spondyloepimetaphyseal dysplasia
P10909	Clusterin	AAG4 APOJ CLI CLU KUB1	14	293	atherosclerosis breast cancer diabetic retinopathy exfoliation syndrome hypertension inclusion body myositis muscular disease myocardial infarction pre-eclampsia
P02787	Serotransferrin	PRO1400 TF	8	293	anemia atransferrinemia gastrointestinal system disease hyperglycemia iron deficiency anemia restless legs syndrome type 1 diabetes mellitus
P51884	Lumican	LDC LUM SLRR2D	8	295	carotid artery disease coronary artery disease pancreatic cancer
P07602	Prosaposin	GLBA PSAP SAP1	23	297	atypical Gaucher's disease due to saposin c deficiency combined saposin deficiency late onset Parkinson's disease metachromatic leukodystrophy
P00738	Haptoglobin	HP	8	298	Plasmodium falciparum malaria arteriosclerosis gout hemolytic anemia hyperglycemia hypertension myocardial infarction pre-eclampsia pulmonary hypertension
P13473	Lysosome-associated membrane glycoprotein 2	LAMP2	33	311	Danon disease hypertrophic cardiomyopathy

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