GlyCosmos Portal

Source	Last Updated
GlyConnect	March 24, 2025
GlycoProtDB	December 4, 2018
GlyGen	October 30, 2024
The O-GlcNAc Database	January 30, 2025
UniProt	February 20, 2025

Displaying entries **26 - 50** of **139028** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology ▲
P33076	MHC class II transactivator	CIITA MHC2TA	Homo sapiens (human)	5	1	Addison's disease MHC class II deficiency juvenile rheumatoid arthritis multiple sclerosis myocardial infarction rheumatoid arthritis systemic lupus erythematosus
Q2KHT3	Protein CLEC16A	CLEC16A KIAA0350	Homo sapiens (human)	3	1	Addison's disease multiple sclerosis rheumatoid arthritis type 1 diabetes mellitus
Q9Y3Z3	Deoxynucleoside triphosphate triphosphohydrolase SAMHD1	MOP5 SAMHD1	Homo sapiens (human)	4	1	Aicardi-Goutieres syndrome Chilblain lupus acute myeloid leukemia hepatitis B hepatitis C
P55265	Double-stranded RNA-specific adenosine deaminase	ADAR ADAR1 DSRAD G1P1 IFI4	Homo sapiens (human)	13	2	Aicardi-Goutieres syndrome Human papillomavirus infectious disease dyschromatosis symmetrica hereditaria liver cirrhosis
Q99MU3	Double-stranded RNA-specific adenosine deaminase	Adar	Mus musculus (house mouse)	2	1	Aicardi-Goutieres syndrome
P78504	Protein jagged-1	JAG1 JAGL1	Homo sapiens (human)	13	5	Alagille syndrome Charcot-Marie-Tooth disease congenital heart disease multiple sclerosis tetralogy of Fallot
Q04721	Neurogenic locus notch homolog protein 2	NOTCH2	Homo sapiens (human)	18	8	Alagille syndrome Hajdu-Cheney syndrome
Q9QXX0	Protein jagged-1	Jag1	Mus musculus (house mouse)	10	4	Alagille syndrome
O60840	Voltage-dependent L-type calcium channel subunit alpha-1F	CACNA1F CACNAF1	Homo sapiens (human)	1	0	Aland Island eye disease X-linked cone-rod dystrophy 3 congenital stationary night blindness 2A congenital stationary night blindness
P03995	Glial fibrillary acidic protein	Gfap	Mus musculus (house mouse)	1	1	Alexander disease
P14136	Glial fibrillary acidic protein	GFAP	Homo sapiens (human)	1	1	Alexander disease
Q2LD37	Bridge-like lipid transfer protein family member 1	BLTP1 FSA KIAA1109 KIAA1371 TWEEK	Homo sapiens (human)	4	1	Alkuraya-Kucinskas syndrome
P29400	Collagen alpha-5(IV) chain	COL4A5	Homo sapiens (human)	10	1	Alport syndrome X-linked Alport syndrome
Q01955	Collagen alpha-3(IV) chain	COL4A3	Homo sapiens (human)	11	1	Alport syndrome autosomal dominant Alport syndrome autosomal recessive Alport syndrome benign familial hematuria end stage renal disease
Q8K4E0	Centrosome-associated protein ALMS1	Alms1 Kiaa0328	Mus musculus (house mouse)	10	1	Alstrom syndrome obesity
Q8TCU4	Centrosome-associated protein ALMS1	ALMS1 KIAA0328	Homo sapiens (human)	44	3	Alstrom syndrome
P00749	Urokinase-type plasminogen activator	PLAU	Homo sapiens (human)	5	31	Alzheimer's disease 1 Alzheimer's disease Quebec platelet disorder adult respiratory distress syndrome end stage renal disease lung non-small cell carcinoma mitral valve prolapse myocardial infarction peritonitis pleural empyema pulmonary fibrosis urinary bladder cancer urolithiasis
P14599	Amyloid-beta-like protein	Appl CG7727	Drosophila melanogaster (fruit fly)	5	0	Alzheimer's disease 1 Alzheimer's disease
P05164	Myeloperoxidase	MPO	Homo sapiens (human)	10	69	Alzheimer's disease 1 acute kidney failure asthma cardiovascular system disease cystic fibrosis end stage renal disease hepatocellular carcinoma keratosis liver cirrhosis lung cancer lung disease lupus nephritis pancreatic cancer vasculitis
Q9NZC2	Triggering receptor expressed on myeloid cells 2	TREM2	Homo sapiens (human)	2	0	Alzheimer's disease 17
O14672	Disintegrin and metalloproteinase domain-containing protein 10	ADAM10 KUZ MADM	Homo sapiens (human)	15	58	Alzheimer's disease 18 reticulate acropigmentation of Kitamura
P02649	Apolipoprotein E	APOE	Homo sapiens (human)	11	6	Alzheimer's disease 2 Alzheimer's disease 3 Alzheimer's disease Kuhnt-Junius degeneration Sjogren's syndrome abdominal aortic aneurysm age related macular degeneration 1 amyotrophic lateral sclerosis angle-closure glaucoma atherosclerosis atopic dermatitis bile duct cancer breast cancer cerebral infarction cerebrovascular disease cholelithiasis congestive heart failure coronary artery disease diabetes mellitus diabetic retinopathy dilated cardiomyopathy exfoliation syndrome familial combined hyperlipidemia gallbladder cancer herpes simplex virus keratitis herpes simplex hyperlipoproteinemia type III hyperuricemia low tension glaucoma lung carcinoma macular degeneration malaria multiple myeloma myocardial infarction open-angle glaucoma primary open angle glaucoma psoriasis retinal disease sea-blue histiocytosis sensorineural hearing loss
O02194	Presenilin homolog	CG18803 PS Psn	Drosophila melanogaster (fruit fly)	1	0	Alzheimer's disease 3 Alzheimer's disease dilated cardiomyopathy early-onset Parkinson's disease
Q8IZY2	Phospholipid-transporting ATPase ABCA7	ABCA7	Homo sapiens (human)	10	5	Alzheimer's disease 9
P35355	Prostaglandin G/H synthase 2	Cox-2 Cox2 Ptgs2	Rattus norvegicus (Norway rat)	4	0	Alzheimer's disease Barrett's esophagus Huntington's disease Parkinsonism Wernicke encephalopathy acute kidney failure adenocarcinoma brain ischemia cystitis diabetic neuropathy endometriosis gastric ulcer gastritis hypertension lung cancer nephrotic syndrome pleurisy polycystic kidney disease portal hypertension pulmonary emphysema pulmonary hypertension retrograde amnesia secondary hyperparathyroidism status epilepticus steatotic liver disease ulcerative colitis

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