GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of GlyTouCan IDs	Disease Ontology
Q5VV67	Peroxisome proliferator-activated receptor gamma coactivator-related protein 1	PPRC1 KIAA0595	1
Q86SG5	Protein S100-A7A	S100A7A S100A15 S100A7L1	1
Q8NAB2	Kelch repeat and BTB domain-containing protein 3	KBTBD3 BKLHD3	1
Q68EA5	Zinc finger protein 57	ZNF57 ZNF424	1
Q8TDJ5	Tyrosine-protein kinase receptor	TFG/ALK fusion	1
Q8IZV5	Retinol dehydrogenase 10	RDH10 SDR16C4	1
Q6WKZ4	Rab11 family-interacting protein 1	RAB11FIP1 RCP	1
Q8N1Q8	Acyl-coenzyme A thioesterase THEM5	THEM5 ACOT15	1	catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia steatotic liver disease
Q8N1L9	Basic leucine zipper transcriptional factor ATF-like 2	BATF2	1
P98179	RNA-binding protein 3	RBM3 RNPL	1
P32121	Beta-arrestin-2	ARRB2 ARB2 ARR2	1
Q92636	Protein FAN	NSMAF FAN	1
P41240	Tyrosine-protein kinase CSK	CSK	1
P54710	Sodium/potassium-transporting ATPase subunit gamma	FXYD2 ATP1C ATP1G1	1
Q6ZUT9	DENN domain-containing protein 5B	DENND5B	1
O75461	Transcription factor E2F6	E2F6	1
O95394	Phosphoacetylglucosamine mutase	PGM3 AGM1	1	Desbuquois dysplasia Laron syndrome MHC class II deficiency Richter's syndrome achondroplasia adenosine deaminase deficiency agranulocytosis allergic asthma allergic rhinitis asthma atopic dermatitis bacterial sepsis breast cancer breast carcinoma bronchiectasis central nervous system lymphoma chronic ethmoiditis chronic lymphocytic leukemia chronic sphenoidal sinusitis chronic ulcer of skin combined T cell and B cell immunodeficiency congenital disorder of glycosylation cystic fibrosis dermatitis epilepsy esophagitis gastroesophageal reflux disease granuloma annulare hemolytic anemia hyper IgE recurrent infection syndrome 1 hypereosinophilic syndrome intellectual disability intrinsic asthma lactose intolerance learning disability lymphoma lymphopenia membranoproliferative glomerulonephritis mucopolysaccharidosis IV multiple epiphyseal dysplasia neuropathy neutropenia obsolete ymphosarcoma osteochondrodysplasia osteomyelitis otitis media pancytopenia peptic esophagitis peripheral nervous system disease polyneuropathy primary immunodeficiency disease scoliosis sensorineural hearing loss severe combined immunodeficiency severe congenital neutropenia subacute sclerosing panencephalitis vasomotor rhinitis visual epilepsy
O00483	Cytochrome c oxidase subunit NDUFA4	NDUFA4	1
Q8N140	EP300-interacting inhibitor of differentiation 3	EID3	1
Q6PGP7	Superkiller complex protein 3	SKIC3 KIAA0372 TTC37	1
Q56A73	Spindlin-4	SPIN4	1
Q8TAS1	Serine/threonine-protein kinase Kist	UHMK1 KIS KIST	1
P55209	Nucleosome assembly protein 1-like 1	NAP1L1 NRP	1
Q9P032	NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 4	NDUFAF4 C6orf66 HRPAP20	1
P13805	Troponin T, slow skeletal muscle	TNNT1 TNT	1

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