GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
Q15366	Poly(rC)-binding protein 2	PCBP2	3	3
Q7Z6A9	B- and T-lymphocyte attenuator	BTLA	3	0
O95405	Zinc finger FYVE domain-containing protein 9	ZFYVE9 MADHIP SARA SMADIP	3	3
Q5T1J5	Putative coiled-coil-helix-coiled-coil-helix domain-containing protein CHCHD2P9, mitochondrial	CHCHD2P9 C9orf49 CHCHD9	3	1
A4FVC6	ABCA6 protein (Fragment)	ABCA6	3	0
Q9Y3N9	Olfactory receptor 2W1	OR2W1	3	1
Q9UBN6	Tumor necrosis factor receptor superfamily member 10D	TNFRSF10D DCR2 TRAILR4 TRUNDD	3	1
Q9H252	Potassium voltage-gated channel subfamily H member 6	KCNH6 ERG2	3	1
Q86VH5	Leucine-rich repeat transmembrane neuronal protein 3	LRRTM3	3	1
P0DTE5	UDP-glucuronosyltransferase 2A2	UGT2A2	3	0
C8C061	Bone morphogenetic protein 2	BMP2	3	0
P29460	Interleukin-12 subunit beta	IL12B NKSF2	3	1
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
Q9HBL0	Tensin-1	TNS1 TNS	3	1
Q96FL9	Polypeptide N-acetylgalactosaminyltransferase 14	GALNT14	3	3	Balo concentric sclerosis Cockayne syndrome Cornelia de Lange syndrome 1 Cornelia de Lange syndrome Dubowitz syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome acute myeloid leukemia adrenoleukodystrophy autistic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome basal cell carcinoma breast cancer breast carcinoma cancer central nervous system disease chondrodysplasia-pseudohermaphroditism syndrome colorectal cancer colorectal carcinoma corneal disease embryoma esophagus squamous cell carcinoma giant cell glioblastoma glioblastoma hepatocellular carcinoma high grade glioma keratoconus large intestine cancer liver cancer liver carcinoma lung adenocarcinoma lung cancer lung non-small cell carcinoma melanoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II narcolepsy neuroblastoma otitis media ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma signet ring cell adenocarcinoma skin melanoma
Q6IMN6	Caprin-2	CAPRIN2 C1QDC1 EEG1 KIAA1873 RNG140	3	1
A0A7D9G5L2	MHC Class I chain-related protein	MICA	3	0
B0YJ32	Laminin alpha-3 chain variant 1	LAMA3	3	0
A6NC57	Ankyrin repeat domain-containing protein 62	ANKRD62	3	5
Q9ULW2	Frizzled-10	FZD10	3	0
A0A385JFK4	MHC Class I chain-related protein	MICA	3	0
P11049	Leukocyte antigen CD37	CD37 TSPAN26	3	0
X5DQS5	Cell adhesion molecule 1 (Fragment)	CADM1	3	0
Q9Y6Q5	AP-1 complex subunit mu-2	AP1M2	3	1
Q96JB2	Conserved oligomeric Golgi complex subunit 3	COG3 SEC34	3	1	autosomal recessive limb-girdle muscular dystrophy type 2A breast cancer cancer

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