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 **1351 - 1375** of **18496** in total

« First

‹ Prev

…

51

52

53

54

55

56

57

58

59

…

Next ›

Last »
UniProt ID ▼	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
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
Q9P1D8	Putative uncharacterized protein PRO2289	PRO2289	Homo sapiens (human)	2	1
Q9P1A6	Disks large-associated protein 2	DLGAP2 C8orf68 DAP2 ERICH1-AS1	Homo sapiens (human)	3	3
Q9P126	C-type lectin domain family 1 member B	CLEC1B CLEC2	Homo sapiens (human)	3	1	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 Evans' syndrome Marfan syndrome Pick's disease Reye syndrome adult respiratory distress syndrome androgen insensitivity syndrome arteriosclerotic cardiovascular disease atherosclerosis atrioventricular septal defect autoimmune thrombocytopenic purpura bacterial sepsis blood coagulation disease cancer cerebral degeneration cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coronary artery disease diabetes mellitus diabetic ketoacidosis embryoma gallbladder disease hematopoietic system disease hemolytic-uremic syndrome hepatocellular carcinoma liver cancer liver disease lung benign neoplasm melanoma newborn respiratory distress syndrome nonpapillary renal cell carcinoma nutmeg liver obsolete inherited blood coagulation disease papillary renal cell carcinoma pneumonia renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid renal cell carcinoma situs inversus skin melanoma split hand-foot malformation 1 stomach cancer stomach carcinoma thrombocytopenia due to platelet alloimmunization thrombocytopenia thrombophilia thrombotic thrombocytopenic purpura tuberous sclerosis type 2 diabetes mellitus viral infectious disease
Q9P121	Neurotrimin	NTM IGLON2 NT	Homo sapiens (human)	7	0	Kartagener syndrome Mycobacterium avium complex disease Parkinson's disease acquired immunodeficiency syndrome actinic keratosis acute myeloid leukemia acute myocardial infarction attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bronchiectasis cancer chronic obstructive pulmonary disease congenital aphakia congenital heart disease congestive heart failure coronary thrombosis depressive disorder embryoma endophthalmitis esophagitis familial medullary thyroid carcinoma gallbladder disease gastroesophageal reflux disease hepatocellular carcinoma intracranial aneurysm late onset Parkinson's disease leprosy liver cancer liver disease lung disease lymphadenitis major depressive disorder melancholic depression multiple endocrine neoplasia type 2A myocardial infarction myopia neurotic disorder nicotine dependence obsolete melancholia peptic esophagitis primary ciliary dyskinesia 1 primary ciliary dyskinesia primary open angle glaucoma pulmonary tuberculosis schizophrenia seborrheic keratosis silent myocardial infarction skin disease thyroid gland medullary carcinoma tuberculosis tuberculous pneumothorax
Q9P109	Beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 4	GCNT4	Homo sapiens (human)	2	0
Q9P0X4	Voltage-dependent T-type calcium channel subunit alpha-1I	CACNA1I KIAA1120	Homo sapiens (human)	7	1
Q9P0W2	SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1-related	HMG20B BRAF35 HMGX2 HMGXB2 SMARCE1R	Homo sapiens (human)	0	1
Q9P0V9	Septin-10	SEPTIN10 SEPT10	Homo sapiens (human)	0	1
Q9P0V8	SLAM family member 8	SLAMF8 BLAME	Homo sapiens (human)	1	1

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements