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 **16576 - 16600** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
P48378	DNA-binding protein RFX2	RFX2	Homo sapiens (human)	1
P29992	Guanine nucleotide-binding protein subunit alpha-11	GNA11 GA11	Homo sapiens (human)	1
Q9ULE6	Paladin	PALD1 KIAA1274 PALD	Homo sapiens (human)	1
P22059	Oxysterol-binding protein 1	OSBP OSBP1	Homo sapiens (human)	1
Q00005	Serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B beta isoform	PPP2R2B	Homo sapiens (human)	1
Q86W50	RNA N6-adenosine-methyltransferase METTL16	METTL16 METT10D	Homo sapiens (human)	1
Q969Q0	Ribosomal protein eL42-like	RPL36AL	Homo sapiens (human)	1
Q9Y2D2	UDP-N-acetylglucosamine transporter	SLC35A3	Homo sapiens (human)	1	Marfan syndrome autism spectrum disorder autistic disorder central nervous system cancer congenital disorder of glycosylation epilepsy gliosarcoma high grade glioma intellectual disability learning disability microcephaly mixed glioma mucopolysaccharidosis IV multiple epiphyseal dysplasia osteochondrodysplasia scoliosis situs inversus spondylocostal dysostosis syndromic X-linked intellectual disability 94 tuberous sclerosis visual epilepsy
Q15697	Zinc finger protein 174	ZNF174 ZSCAN8	Homo sapiens (human)	1
Q9H0E7	Ubiquitin carboxyl-terminal hydrolase 44	USP44	Homo sapiens (human)	1
P49753	Acyl-coenzyme A thioesterase 2, mitochondrial	ACOT2 PTE2 PTE2A	Homo sapiens (human)	1	coronary artery disease diabetes mellitus type 2 diabetes mellitus
O60765	Zinc finger protein 354A	ZNF354A EZNF HKL1 TCF17	Homo sapiens (human)	1
A0A087WWU8	Tropomyosin 3	TPM3	Homo sapiens (human)	1
Q8N616	Putative uncharacterized protein encoded by LINC00311	LINC00311 NCRNA00311 TMEM148	Homo sapiens (human)	1
Q8TCT1	Phosphoethanolamine/phosphocholine phosphatase	PHOSPHO1	Homo sapiens (human)	1	diabetes mellitus osteomalacia rickets type 2 diabetes mellitus
Q9UPM6	LIM/homeobox protein Lhx6	LHX6 LHX6.1	Homo sapiens (human)	1
P05161	Ubiquitin-like protein ISG15	ISG15 G1P2 UCRP	Homo sapiens (human)	1
E9PRG8	Uncharacterized protein C11orf98	C11orf98	Homo sapiens (human)	1
P41743	Protein kinase C iota type	PRKCI DXS1179E	Homo sapiens (human)	1
Q9H2Z4	Homeobox protein Nkx-2.4	NKX2-4 NKX2D	Homo sapiens (human)	1
Q9Y330	Zinc finger and BTB domain-containing protein 12	ZBTB12 C6orf46 G10 NG35	Homo sapiens (human)	1
Q8N6N3	UPF0690 protein C1orf52	C1orf52 BAG	Homo sapiens (human)	1
Q9Y3B4	Splicing factor 3B subunit 6	SF3B6 SAP14 SF3B14 SF3B14A	Homo sapiens (human)	1
Q00577	Transcriptional activator protein Pur-alpha	PURA PUR1	Homo sapiens (human)	1
Q15147	1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-4	PLCB4	Homo sapiens (human)	1	46,XY sex reversal Chagas disease Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Kawasaki disease abdominal obesity-metabolic syndrome 1 absence epilepsy acute chest syndrome acute myeloid leukemia adenocarcinoma adenoma agenesis of the corpus callosum with peripheral neuropathy agnosia ankylosis bipolar disorder breast cancer breast carcinoma cancer central sleep apnea childhood absence epilepsy childhood acute myeloid leukemia cleft palate congenital ptosis coronary aneurysm cribriform carcinoma cutaneous fibrous histiocytoma dengue hemorrhagic fever depressive disorder embryoma endometriosis of uterus endometriosis essential thrombocythemia gastrointestinal stromal tumor granular cell carcinoma hereditary neuropathy with liability to pressure palsies hidradenoma isolated cleft palate lung cancer lung non-small cell carcinoma major depressive disorder melancholic depression melanoma mood disorder motor peripheral neuropathy myelodysplastic syndrome neurotic disorder obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia obstructive sleep apnea ptosis schizoaffective disorder schizophrenia schizophreniform disorder sensorineural hearing loss skin melanoma skin papilloma skin tag syringoma tongue disease trypanosomiasis tubular adenocarcinoma uveal melanoma

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