GlyCosmos Portal

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UniProt ID ▲	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9NR64	Kelch-like protein 1	KLHL1 KIAA1490	1	1
Q9NR71	Neutral ceramidase	ASAH2 HNAC1	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
Q9NR80	Rho guanine nucleotide exchange factor 4	ARHGEF4 KIAA1112	2	1
Q9NR81	Rho guanine nucleotide exchange factor 3	ARHGEF3	0	1
Q9NR82	Potassium voltage-gated channel subfamily KQT member 5	KCNQ5	1	1
Q9NR96	Toll-like receptor 9	TLR9	14	5
Q9NR97	Toll-like receptor 8	TLR8	23	9
Q9NR99	Matrix-remodeling-associated protein 5	MXRA5	44	60
Q9NRA1	Platelet-derived growth factor C	PDGFC SCDGF	3	5
Q9NRA2	Sialin	SLC17A5	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
Q9NRA8	Eukaryotic translation initiation factor 4E transporter	EIF4ENIF1	5	1
Q9NRB3	Carbohydrate sulfotransferase 12	CHST12	7	5	lupus erythematosus systemic lupus erythematosus
Q9NRC1	Suppressor of tumorigenicity 7 protein	ST7 FAM4A1 HELG RAY1	1	0
Q9NRC6	Spectrin beta chain, non-erythrocytic 5	SPTBN5 BSPECV HUBSPECV HUSPECV	1	2
Q9NRC8	NAD-dependent protein deacetylase sirtuin-7	SIRT7 SIR2L7	3	1
Q9NRD8	Dual oxidase 2	DUOX2 LNOX2 THOX2	6	1
Q9NRD9	Dual oxidase 1	DUOX1 DUOX LNOX1 THOX1	6	1
Q9NRE1	Matrix metalloproteinase-26	MMP26	2	0
Q9NRE2	Teashirt homolog 2	TSHZ2 C20orf17 TSH2 ZNF218	1	1
Q9NRF2	SH2B adapter protein 1	SH2B1 KIAA1299 SH2B	1	1
Q9NRF8	CTP synthase 2	CTPS2	0	1
Q9NRF9	DNA polymerase epsilon subunit 3	POLE3 CHRAC17	1	2
Q9NRG0	Chromatin accessibility complex protein 1	CHRAC1 CHRAC15	0	1
Q9NRG4	N-lysine methyltransferase SMYD2	SMYD2 KMT3C	0	1
Q9NRG9	Aladin	AAAS ADRACALA	2	1

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