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 **1751 - 1775** 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
Q9NRF8	CTP synthase 2	CTPS2	Homo sapiens (human)	0	1
Q9NRF2	SH2B adapter protein 1	SH2B1 KIAA1299 SH2B	Homo sapiens (human)	1	1
Q9NRE2	Teashirt homolog 2	TSHZ2 C20orf17 TSH2 ZNF218	Homo sapiens (human)	1	1
Q9NRE1	Matrix metalloproteinase-26	MMP26	Homo sapiens (human)	2	0
Q9NRD9	Dual oxidase 1	DUOX1 DUOX LNOX1 THOX1	Homo sapiens (human)	6	1
Q9NRD8	Dual oxidase 2	DUOX2 LNOX2 THOX2	Homo sapiens (human)	6	1
Q9NRC8	NAD-dependent protein deacetylase sirtuin-7	SIRT7 SIR2L7	Homo sapiens (human)	3	1
Q9NRC6	Spectrin beta chain, non-erythrocytic 5	SPTBN5 BSPECV HUBSPECV HUSPECV	Homo sapiens (human)	1	2
Q9NRC1	Suppressor of tumorigenicity 7 protein	ST7 FAM4A1 HELG RAY1	Homo sapiens (human)	1	0
Q9NRB3	Carbohydrate sulfotransferase 12	CHST12	Homo sapiens (human)	7	5	lupus erythematosus systemic lupus erythematosus
Q9NRA8	Eukaryotic translation initiation factor 4E transporter	EIF4ENIF1	Homo sapiens (human)	5	1
Q9NRA2	Sialin	SLC17A5	Homo sapiens (human)	3	0	Alzheimer's disease Balo concentric sclerosis Crimean-Congo hemorrhagic fever Gilbert syndrome HELLP syndrome IgA glomerulonephritis Japanese encephalitis Lassa fever Parkinson's disease Plasmodium falciparum malaria Reye syndrome Stevens-Johnson syndrome Wilson disease abdominal obesity-metabolic syndrome 1 acrodermatitis acute pancreatitis adrenoleukodystrophy agammaglobulinemia agranulocytosis alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis allergic asthma alternating exotropia amelogenesis imperfecta type 1E amnestic disorder amyotrophic lateral sclerosis type 1 anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autoimmune hepatitis autoimmune polyendocrine syndrome bilirubin metabolic disorder cancer cardiovascular system disease cataract 2 multiple types cataract 30 cataract 32 multiple types central nervous system disease cerebral degeneration cerebral infarction cerebrovascular disease cholestasis chromosome 17p13.1 deletion syndrome chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer common cold communicating hydrocephalus congenital nystagmus congenital ptosis congestive heart failure coronary artery disease dementia dengue disease dengue hemorrhagic fever depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis diarrhea disease of metabolism disseminated intravascular coagulation dissociated nystagmus dysthymic disorder embryoma epilepsy essential hypertension essential thrombocythemia exotropia familial hyperlipidemia familial nephrotic syndrome fascioliasis fibromyalgia gallbladder disease gingival hypertrophy gingival overgrowth glomerulonephritis glucose intolerance glycogen storage disease II head and neck squamous cell carcinoma heart disease hemochromatosis hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma hydrocephalus hyperglycemia hypertension hypohidrotic ectodermal dysplasia immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome intellectual disability intrahepatic cholestasis of pregnancy intrinsic asthma iron metabolism disease kidney disease kidney failure large intestine cancer late onset Parkinson's disease learning disability leukodystrophy leukopenia lipoid nephrosis lissencephaly liver cancer liver carcinoma liver cirrhosis liver disease lung cancer lung non-small cell carcinoma lymphopenia lysosomal storage disease macrocytic anemia major depressive disorder medium chain acyl-CoA dehydrogenase deficiency melancholic depression melanoma microphthalmia monocular exotropia myelodysplastic syndrome myocarditis myositis narcolepsy nasopharyngitis nephritis nephrosis nephrotic syndrome neurodegenerative disease neurotic disorder neutropenia obesity obsolete Matthew-Wood syndrome obsolete melancholia obstructive hydrocephalus obstructive sleep apnea osteoarthritis osteomalacia pancreatitis pancytopenia parapsoriasis pathologic nystagmus pneumonia portal vein thrombosis pre-eclampsia prediabetes syndrome primary polycythemia primary sclerosing cholangitis psoriasis ptosis purpura fulminans pustulosis of palm and sole pyoureter retrograde amnesia rheumatoid arthritis rickets sclerosing cholangitis senile degeneration of brain severe congenital neutropenia sialuria sickle cell anemia skin melanoma spontaneous ocular nystagmus steatotic liver disease subcortical band heterotopia thrombocytopenia tuberculosis type 2 diabetes mellitus uremia viral infectious disease visceral leishmaniasis visual epilepsy yellow fever
Q9NRA1	Platelet-derived growth factor C	PDGFC SCDGF	Homo sapiens (human)	3	5
Q9NR99	Matrix-remodeling-associated protein 5	MXRA5	Homo sapiens (human)	44	60
Q9NR97	Toll-like receptor 8	TLR8	Homo sapiens (human)	23	9
Q9NR96	Toll-like receptor 9	TLR9	Homo sapiens (human)	14	5
Q9NR82	Potassium voltage-gated channel subfamily KQT member 5	KCNQ5	Homo sapiens (human)	1	1
Q9NR81	Rho guanine nucleotide exchange factor 3	ARHGEF3	Homo sapiens (human)	0	1
Q9NR80	Rho guanine nucleotide exchange factor 4	ARHGEF4 KIAA1112	Homo sapiens (human)	2	1
Q9NR71	Neutral ceramidase	ASAH2 HNAC1	Homo sapiens (human)	23	0	Alzheimer's disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome celiac disease colorectal cancer congenital diaphragmatic hernia cystic fibrosis dementia diabetes mellitus diabetic ketoacidosis gallbladder disease gamma heavy chain disease glaucoma heavy chain disease inflammatory bowel disease large intestine cancer liver disease lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 neuroblastoma obesity systemic Epstein-Barr virus positive T-cell lymphoma of childhood type 2 diabetes mellitus
Q9NR64	Kelch-like protein 1	KLHL1 KIAA1490	Homo sapiens (human)	1	1
Q9NR61	Delta-like protein 4	DLL4	Homo sapiens (human)	4	0
Q9NR56	Muscleblind-like protein 1	MBNL1 EXP KIAA0428 MBNL	Homo sapiens (human)	1	1
Q9NR50	Translation initiation factor eIF2B subunit gamma	EIF2B3	Homo sapiens (human)	0	1
Q9NR48	Histone-lysine N-methyltransferase ASH1L	ASH1L KIAA1420 KMT2H	Homo sapiens (human)	2	3

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