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 **1701 - 1725** 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
H3BSZ0	Transmembrane protein 87A	TMEM87A	Homo sapiens (human)	2	0
Q6ZMM2	ADAMTS-like protein 5	ADAMTSL5 THSD6	Homo sapiens (human)	2	2
Q9P242	Neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 2	NYAP2 KIAA1486	Homo sapiens (human)	1	1
P04196	Histidine-rich glycoprotein	HRG	Homo sapiens (human)	7	104
Q96QV6	Histone H2A type 1-A	H2AC1 H2AFR HIST1H2AA	Homo sapiens (human)	1	2
Q7Z6K4	Notch-regulated ankyrin repeat-containing protein	NRARP	Homo sapiens (human)	1	1
Q96BF3	Transmembrane and immunoglobulin domain-containing protein 2	TMIGD2 CD28H IGPR1	Homo sapiens (human)	3	0
Q9Y672	Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase	ALG6	Homo sapiens (human)	1	0	antithrombin III deficiency congenital disorder of glycosylation Ia congenital disorder of glycosylation Ic congenital disorder of glycosylation type I congenital disorder of glycosylation epilepsy hypertropia mechanical strabismus ophthalmoplegia protein C deficiency protein S deficiency strabismus thrombophilia visual epilepsy
Q8WVV4	Protein POF1B	POF1B	Homo sapiens (human)	0	1
A0A1C8DTU5	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
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
C9JDK4	Autophagy-related protein 9 (Fragment)	ATG9A	Homo sapiens (human)	1	0
P30408	Transmembrane 4 L6 family member 1	TM4SF1 M3S1 TAAL6	Homo sapiens (human)	2	0
Q9H8Y5	tRNA endonuclease ANKZF1	ANKZF1 ZNF744	Homo sapiens (human)	1	1
Q9BQS2	Synaptotagmin-15	SYT15	Homo sapiens (human)	0	1
Q19K85	MHC class I antigen (Fragment)	HLA-Cw	Homo sapiens (human)	1	0
Q8NDV7	Trinucleotide repeat-containing gene 6A protein	TNRC6A CAGH26 KIAA1460 TNRC6	Homo sapiens (human)	22	5
Q6ZS27	Zinc finger protein 662	ZNF662	Homo sapiens (human)	0	1
Q9Y3B8	Oligoribonuclease, mitochondrial	REXO2 SFN SMFN	Homo sapiens (human)	0	1
Q14590	Zinc finger protein 235	ZNF235 ZFP93 ZNF270	Homo sapiens (human)	0	1
H0Y5D1	Complement C1s (Fragment)	C1S	Homo sapiens (human)	1	0
Q5T848	Metabotropic glycine receptor	GPR158 KIAA1136	Homo sapiens (human)	5	0
A0A2H4G436	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
A0A804HIZ0	Voltage-dependent L-type calcium channel subunit alpha	CACNA1C	Homo sapiens (human)	1	0
Q9Y3D8	Adenylate kinase isoenzyme 6	AK6 CINAP	Homo sapiens (human)	0	1

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