GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol ▲	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9Y666	Solute carrier family 12 member 7	SLC12A7 KCC4	3	7
A0AV02	Solute carrier family 12 member 8	SLC12A8 CCC9	1	0
Q9BXP2	Solute carrier family 12 member 9	SLC12A9 CCC6 CIP1	2	3
Q9BZW2	Solute carrier family 13 member 1	SLC13A1 NAS1 NASI1	3	0
Q8WWT9	Na(+)/dicarboxylate cotransporter 3	SLC13A3 NADC3 SDCT2	3	1
Q86YT5	Na(+)/citrate cotransporter	SLC13A5 NACT	1	0
Q13336	Urea transporter 1	SLC14A1 HUT11 JK RACH1 UT1 UTE	2	3
Q15849	Urea transporter 2	SLC14A2 HUT2 UT2	1	0
P46059	Solute carrier family 15 member 1	SLC15A1 PEPT1	7	0
Q16348	Solute carrier family 15 member 2	SLC15A2 PEPT2	5	0
Q8IY34	Solute carrier family 15 member 3	SLC15A3 OCTP PHT2 PTR3	6	0
Q8N697	Solute carrier family 15 member 4	SLC15A4 PHT1 PTR4	2	3
P53985	Monocarboxylate transporter 1	SLC16A1 MCT1	0	1
O15427	Monocarboxylate transporter 4	SLC16A3 MCT3 MCT4	1	1
O60669	Monocarboxylate transporter 2	SLC16A7 MCT2	1	1
Q7RTY1	Monocarboxylate transporter 9	SLC16A9 C10orf36 MCT9	0	1
Q14916	Sodium-dependent phosphate transport protein 1	SLC17A1 NPT1	3	0
O00624	Sodium-dependent phosphate transport protein 3	SLC17A2 NPT3	4	1
O00476	Sodium-dependent phosphate transport protein 4	SLC17A3 NPT4	4	0
Q9Y2C5	Probable small intestine urate exporter	SLC17A4	5	0
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
Q9P2U8	Vesicular glutamate transporter 2	SLC17A6 DNPI VGLUT2	3	0
Q8NDX2	Vesicular glutamate transporter 3	SLC17A8 VGLUT3	1	0
P54219	Chromaffin granule amine transporter	SLC18A1 VAT1 VMAT1	3	0
Q05940	Synaptic vesicular amine transporter	SLC18A2 SVMT VMAT2	2	0

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