GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
Q9NZ32	Actin-related protein 10	ACTR10 ACTR11 ARP10 ARP11	0	1
Q8WV99	AN1-type zinc finger protein 2B	ZFAND2B AIRAPL	2	1
P69892	Hemoglobin subunit gamma-2	HBG2	0	1
Q5SSJ5	Heterochromatin protein 1-binding protein 3	HP1BP3	5	1
Q08050	Forkhead box protein M1	FOXM1 FKHL16 HFH11 MPP2 WIN	1	1
O60609	GDNF family receptor alpha-3	GFRA3	4	1
O95361	Tripartite motif-containing protein 16	TRIM16 EBBP	0	1
Q4J6C6	Prolyl endopeptidase-like	PREPL KIAA0436	0	1
Q04446	1,4-alpha-glucan-branching enzyme	GBE1	0	1	B-cell lymphoma Cauda equina syndrome Fabry disease Gerstmann-Straussler-Scheinker syndrome Gorham's disease Guillain-Barre syndrome Noonan syndrome 1 acute myeloid leukemia bronchus cancer bronchus carcinoma cancer cardiomyopathy carnitine palmitoyltransferase II deficiency cerebral infarction cerebrovascular disease chronic inflammatory demyelinating polyneuritis chronic inflammatory demyelinating polyradiculoneuropathy chronic ulcer of skin chylomicron retention disease congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A congestive heart failure contractures, pterygia, and spondylocarpotarsal fusion syndrome cystinuria cytochrome-c oxidase deficiency disease dementia diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism embryoma endomyocardial fibrosis esophagus squamous cell carcinoma familial lipoprotein lipase deficiency familial periodic paralysis fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease III glycogen storage disease IV glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease VI glycogen storage disease VII glycogen storage disease hypertrophic cardiomyopathy idiopathic scoliosis intellectual disability learning disability leukodystrophy lipid storage disease liver disease locked-in syndrome lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma megaconial type congenital muscular dystrophy melanoma mitochondrial metabolism disease mitochondrial myopathy mitochondrial trifunctional protein deficiency multiple sclerosis muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 myopathy nemaline myopathy neurogenic bladder obsolete ymphosarcoma ovarian cancer ovarian carcinoma paraplegia polyhydramnios porphyria portal hypertension quadriplegia rigid spine muscular dystrophy 1 skin melanoma
Q9UK53	Inhibitor of growth protein 1	ING1	0	1
Q92754	Transcription factor AP-2 gamma	TFAP2C	0	1
Q15696	U2 small nuclear ribonucleoprotein auxiliary factor 35 kDa subunit-related protein 2	ZRSR2 U2AF1-RS2 U2AF1L2 U2AF1RS2 URP	1	1
Q8N910	Putative uncharacterized protein PAK6-AS1	PAK6-AS1 C15orf56	0	1
Q08188	Protein-glutamine gamma-glutamyltransferase E	TGM3	0	1
P00491	Purine nucleoside phosphorylase	PNP NP	0	1	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Chagas disease Evans' syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Lesch-Nyhan syndrome MELAS syndrome MHC class II deficiency Nezelof syndrome Omenn syndrome Pick's disease Reye syndrome Richter's syndrome T cell deficiency acute lymphoblastic leukemia adenosine deaminase deficiency adult lymphoma agammaglobulinemia agnosia alternating hemiplegia of childhood anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autoimmune disease autoimmune hemolytic anemia autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura autonomic neuropathy bladder carcinoma breast cancer breast carcinoma cancer carcinoma carotid artery disease central nervous system disease central nervous system lymphoma central nervous system vasculitis central retinal vein occlusion cerebral degeneration cerebral malaria cerebral palsy childhood acute lymphocytic leukemia childhood lymphoma chronic lymphocytic leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer combined T cell and B cell immunodeficiency coronary artery disease critical illness polyneuropathy cutaneous leishmaniasis cyclic hematopoiesis developmental coordination disorder diabetic cataract diabetic retinopathy disease of metabolism embryoma esophageal cancer esophageal carcinoma fetal erythroblastosis gangliosidosis giant cell glioblastoma glioblastoma granulomatous angiitis head and neck squamous cell carcinoma hematologic cancer hepatocellular carcinoma herpes simplex high grade glioma hyperuricemia immune system disease inflammatory and toxic neuropathy intellectual disability large intestine cancer learning disability liver cancer locked-in syndrome lupus erythematosus lymphoblastic lymphoma lymphoma lymphopenia macrocytic anemia malaria maxillary sinus squamous cell carcinoma melanoma meningoencephalitis molybdenum cofactor deficiency type A monoclonal gammopathy of uncertain significance nervous system disease neuroblastoma neurodegenerative disease neuropathy obsolete T lymphocyte deficiency obsolete T-cell lymphoblastic leukemia/lymphoma obsolete ymphosarcoma osteoporosis otitis media ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma periodontal disease periodontitis peripheral T-cell lymphoma peripheral nervous system disease phosphoribosylpyrophosphate synthetase superactivity pneumonia polyneuropathy primary immunodeficiency disease prostate cancer prostate carcinoma purine nucleoside phosphorylase deficiency purine-pyrimidine metabolic disorder quadriplegia reflex sympathetic dystrophy retinal vein occlusion sarcomatoid carcinoma severe combined immunodeficiency sinusitis skin melanoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy substance abuse substance-related disorder systemic lupus erythematosus thyroid gland medullary carcinoma trypanosomiasis tuberculosis urinary bladder cancer urinary tract obstruction vascular disease
Q9Y662	Heparan sulfate glucosamine 3-O-sulfotransferase 3B1	HS3ST3B1 3OST3B1 HS3ST3B	5	1	bladder carcinoma breast cancer endometriosis of ovary endometriosis of uterus endometriosis hepatitis B lung cancer lung non-small cell carcinoma pancreatic cancer pancreatic carcinoma urinary bladder cancer
P23560	Brain-derived neurotrophic factor	BDNF	1	1
Q8NA61	Protein chibby homolog 2	CBY2 SPERT	1	1
P28072	Proteasome subunit beta type-6	PSMB6 LMPY Y	0	1
Q9NRW3	DNA dC->dU-editing enzyme APOBEC-3C	APOBEC3C APOBEC1L PBI	0	1
O75153	Clustered mitochondria protein homolog	CLUH KIAA0664	0	1
P50219	Motor neuron and pancreas homeobox protein 1	MNX1 HLXB9	2	1
Q96FN5	Kinesin-like protein KIF12	KIF12	0	1
Q9NXC5	GATOR2 complex protein MIOS	MIOS	0	1
Q5SY80	Cation channel sperm-associated auxiliary subunit epsilon	CATSPERE C1orf101	11	1

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