GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **2251 - 2275** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
Q6NXR4	TELO2-interacting protein 2	TTI2 C8orf41	Homo sapiens (human)	1
P50225	Sulfotransferase 1A1	SULT1A1 STP STP1	Homo sapiens (human)	1
Q96KQ7	Histone-lysine N-methyltransferase EHMT2	EHMT2 BAT8 C6orf30 G9A KMT1C NG36	Homo sapiens (human)	1
Q9BZL3	Small integral membrane protein 3	SMIM3 C5orf62 NID67	Homo sapiens (human)	0
P21266	Glutathione S-transferase Mu 3	GSTM3 GST5	Homo sapiens (human)	1
Q5VV67	Peroxisome proliferator-activated receptor gamma coactivator-related protein 1	PPRC1 KIAA0595	Homo sapiens (human)	1
Q86SG5	Protein S100-A7A	S100A7A S100A15 S100A7L1	Homo sapiens (human)	1
Q8NAB2	Kelch repeat and BTB domain-containing protein 3	KBTBD3 BKLHD3	Homo sapiens (human)	1
Q68EA5	Zinc finger protein 57	ZNF57 ZNF424	Homo sapiens (human)	1
Q8TDJ5	Tyrosine-protein kinase receptor	TFG/ALK fusion	Homo sapiens (human)	1
Q8IZV5	Retinol dehydrogenase 10	RDH10 SDR16C4	Homo sapiens (human)	1
Q6WKZ4	Rab11 family-interacting protein 1	RAB11FIP1 RCP	Homo sapiens (human)	1
Q8N1Q8	Acyl-coenzyme A thioesterase THEM5	THEM5 ACOT15	Homo sapiens (human)	1	catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia steatotic liver disease
Q8N1L9	Basic leucine zipper transcriptional factor ATF-like 2	BATF2	Homo sapiens (human)	1
P98179	RNA-binding protein 3	RBM3 RNPL	Homo sapiens (human)	1
P32121	Beta-arrestin-2	ARRB2 ARB2 ARR2	Homo sapiens (human)	1
Q92636	Protein FAN	NSMAF FAN	Homo sapiens (human)	1
P41240	Tyrosine-protein kinase CSK	CSK	Homo sapiens (human)	1
P54710	Sodium/potassium-transporting ATPase subunit gamma	FXYD2 ATP1C ATP1G1	Homo sapiens (human)	1
Q6ZUT9	DENN domain-containing protein 5B	DENND5B	Homo sapiens (human)	1
O75461	Transcription factor E2F6	E2F6	Homo sapiens (human)	1
O95394	Phosphoacetylglucosamine mutase	PGM3 AGM1	Homo sapiens (human)	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	Homo sapiens (human)	1
Q8N140	EP300-interacting inhibitor of differentiation 3	EID3	Homo sapiens (human)	1
Q6PGP7	Superkiller complex protein 3	SKIC3 KIAA0372 TTC37	Homo sapiens (human)	1

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