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 **7851 - 7875** 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
Q9P258	Protein RCC2	RCC2 KIAA1470 TD60	Homo sapiens (human)	2	2
Q9P253	Vacuolar protein sorting-associated protein 18 homolog	VPS18 KIAA1475	Homo sapiens (human)	0	1
Q9P246	Stromal interaction molecule 2	STIM2 KIAA1482	Homo sapiens (human)	1	0
Q9P244	Leucine-rich repeat and fibronectin type III domain-containing protein 1	LRFN1 KIAA1484 SALM2	Homo sapiens (human)	4	4
Q9P243	Zinc finger protein ZFAT	ZFAT KIAA1485 ZFAT1 ZNF406	Homo sapiens (human)	0	1
Q9P242	Neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 2	NYAP2 KIAA1486	Homo sapiens (human)	1	1
Q9P232	Contactin-3	CNTN3 KIAA1496 PANG	Homo sapiens (human)	13	12	ACTH-secreting pituitary adenoma Baraitser-Winter syndrome Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Raynaud disease Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 allergic contact dermatitis anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autistic disorder branchiootic syndrome breast cancer breast carcinoma cancer cardiomyopathy catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia chronic kidney disease colitis cone-rod dystrophy 2 cone-rod dystrophy coronary artery disease depressive disorder diarrhea dilated cardiomyopathy 1B distal arthrogryposis dry eye syndrome dysthymic disorder embryoma endomyocardial fibrosis essential hypertension familial hypertrophic cardiomyopathy fibromyalgia gastroenteritis generalized anxiety disorder giant cell glioblastoma glioblastoma glomerulonephritis high grade glioma hypertension hypertrophic cardiomyopathy ileitis ileocolitis kidney disease long QT syndrome major depressive disorder melancholic depression morbid obesity mosaic variegated aneuploidy syndrome 1 nephritis nephrosis neurotic disorder obesity obsolete melancholia orofaciodigital syndrome I orofaciodigital syndrome X paraplegia parapsoriasis peripheral artery disease phobic disorder pituitary-dependent Cushing's disease pityriasis rubra pilaris post-traumatic stress disorder prolactinoma psoriasis pustulosis of palm and sole pyoureter restless legs syndrome spinal cord disease trichohepatoenteric syndrome 1 trichohepatoenteric syndrome xerophthalmia
Q9P225	Dynein axonemal heavy chain 2	DNAH2 DNAHC2 DNHD3 KIAA1503	Homo sapiens (human)	1	1
Q9P219	Protein Daple	CCDC88C DAPLE KIAA1509	Homo sapiens (human)	7	1
Q9P218	Collagen alpha-1(XX) chain	COL20A1 KIAA1510	Homo sapiens (human)	3	1
Q9P217	Zinc finger SWIM domain-containing protein 5	ZSWIM5 KIAA1511	Homo sapiens (human)	1	1
Q9P212	1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase epsilon-1	PLCE1 KIAA1516 PLCE PPLC	Homo sapiens (human)	3	1	46,XY sex reversal Alzheimer's disease Barrett's esophagus 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 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 3 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 Japanese encephalitis Miller-Dieker lissencephaly syndrome West Nile fever acute myeloid leukemia adenocarcinoma adenoma adenosarcoma agenesis of the corpus callosum with peripheral neuropathy atrophic gastritis bladder carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease chromosome 17p13.1 deletion syndrome chronic kidney disease chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma common wart congestive heart failure cribriform carcinoma cytochrome-c oxidase deficiency disease dengue disease dengue hemorrhagic fever embryoma esophageal cancer esophageal carcinoma esophagitis esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia familial nephrotic syndrome focal segmental glomerulosclerosis gallbladder cancer gallbladder carcinoma gastric adenocarcinoma gastric cardia adenocarcinoma gastric cardia carcinoma gastritis gastroesophageal reflux disease gastrointestinal system cancer glomerulonephritis granular cell carcinoma head and neck squamous cell carcinoma heart disease hepatitis B hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hypertension large intestine cancer lipoid nephrosis lissencephaly liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma migraine mitochondrial metabolism disease motor peripheral neuropathy myelodysplastic syndrome nephritis nephroblastoma nephrotic syndrome type 1 nephrotic syndrome type 2 nephrotic syndrome type 3 nephrotic syndrome obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum open-angle glaucoma peptic esophagitis primary open angle glaucoma proteinuria sarcomatoid carcinoma squamous cell carcinoma squamous cell neoplasm stomach cancer stomach carcinoma temporal arteritis tongue squamous cell carcinoma tubular adenocarcinoma urinary bladder cancer viral infectious disease yellow fever
Q9P202	Whirlin	WHRN DFNB31 KIAA1526	Homo sapiens (human)	1	1
Q9P1Z3	Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3	HCN3 KIAA1535	Homo sapiens (human)	1	1
Q9P1Z2	Calcium-binding and coiled-coil domain-containing protein 1	CALCOCO1 KIAA1536	Homo sapiens (human)	0	1
Q9P1Y6	PHD and RING finger domain-containing protein 1	PHRF1 KIAA1542	Homo sapiens (human)	4	2
Q9P1Y5	Calmodulin-regulated spectrin-associated protein 3	CAMSAP3 KIAA1543	Homo sapiens (human)	5	1
Q9P1W8	Signal-regulatory protein gamma	SIRPG SIRPB2	Homo sapiens (human)	5	1
Q9P1W3	Calcium permeable stress-gated cation channel 1	TMEM63C C14orf171 CSC1	Homo sapiens (human)	1	1
Q9P1U1	Actin-related protein 3B	ACTR3B ARP11 ARP4	Homo sapiens (human)	0	1
Q9P1U0	DNA-directed RNA polymerase I subunit RPA12	POLR1H RPA12 ZNRD1	Homo sapiens (human)	0	1
Q9P1Q5	Olfactory receptor 1A1	OR1A1	Homo sapiens (human)	2	0
Q9P1Q0	Vacuolar protein sorting-associated protein 54	VPS54 HCC8	Homo sapiens (human)	0	1
Q9P1P5	Trace amine-associated receptor 2	TAAR2 GPR58	Homo sapiens (human)	3	0
Q9P1P4	Putative trace amine-associated receptor 3	TAAR3P GPR57 TAAR3	Homo sapiens (human)	1	0

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