GlyCosmos Portal

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GlyConnect	April 19, 2023
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The O-GlcNAc Database	June 3, 2024
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Displaying entries **115201 - 115225** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
Q8N1L9	Basic leucine zipper transcriptional factor ATF-like 2	BATF2	Homo sapiens (human)	0	1
D3Z750	Maestro heat-like repeat-containing protein family member 2A	Mroh2a Heatr7b1	Mus musculus (house mouse)	1	1
P98179	RNA-binding protein 3	RBM3 RNPL	Homo sapiens (human)	0	1
Q4DSE6	Retrotransposon hot spot (RHS) protein	Tc00.1047053504057.90	Trypanosoma cruzi strain CL Brener	0	1
Q8N1I0	Dedicator of cytokinesis protein 4	DOCK4 KIAA0716	Homo sapiens (human)	3	1
Q2TJ65	Superoxide dismutase (Fragment)	FeSODA	Trypanosoma cruzi	0	1
P60891	Ribose-phosphate pyrophosphokinase 1	PRPS1	Homo sapiens (human)	2	1	Arts syndrome 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 2 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 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 type X Charcot-Marie-Tooth disease Foster-Kennedy syndrome Laron syndrome Werner syndrome X-linked nonsyndromic deafness achondroplasia acute lymphoblastic leukemia adult acute lymphocytic leukemia agenesis of the corpus callosum with peripheral neuropathy agnosia alternating exotropia anaplastic astrocytoma blindness breast cancer breast carcinoma cancer carcinoma central sleep apnea childhood acute lymphocytic leukemia childhood cerebral astrocytoma coloboma colorectal cancer colorectal carcinoma communication disorder congenital nystagmus critical illness polyneuropathy developmental coordination disorder diabetes insipidus disease of metabolism dissociated nystagmus embryoma epilepsy exotropia fibrillary astrocytoma fundus dystrophy gemistocytic astrocytoma giant cell glioblastoma glioblastoma gout hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 high grade glioma hyperuricemia inflammatory and toxic neuropathy intellectual disability juvenile pilocytic astrocytoma kidney failure kwashiorkor language disorder large intestine cancer learning disability liver cancer locked-in syndrome malignant astrocytoma marasmus meningoencephalitis monocular exotropia motor peripheral neuropathy neuroblastoma neurodegeneration with brain iron accumulation neurohypophyseal diabetes insipidus neuropathy nutrition disease nutritional optic neuropathy obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum optic atrophy optic nerve disease pancreas disease paraplegia pathologic nystagmus peripheral nervous system disease phosphoribosylpyrophosphate synthetase superactivity pilocytic astrocytoma placental insufficiency polyneuropathy primary immunodeficiency disease progeria protein-energy malnutrition protoplasmic astrocytoma quadriplegia sarcomatoid carcinoma scoliosis sensorineural hearing loss sensory peripheral neuropathy spontaneous ocular nystagmus subependymal giant cell astrocytoma uric acid nephrolithiasis visual epilepsy visual pathway disease
Q9Z2L0	Voltage-dependent anion-selective channel protein 1	Vdac1	Rattus norvegicus (Norway rat)	3	1
A0A0B4K707	Nuak1 ortholog, isoform F	Nuak CG11870 CG11871 CG11872 Dmel\CG43143 EMK/KIAA0537 NUAK Nuak1 Omphk1	Drosophila melanogaster (fruit fly)	0	1
P32121	Beta-arrestin-2	ARRB2 ARB2 ARR2	Homo sapiens (human)	0	1
E1BQ16	O-GlcNAcase	OGA	Bos taurus (cattle)	2	1
D3Z067	ADP-ribosylation factor-like protein 6 (Fragment)	Arl6	Mus musculus (house mouse)	0	1
V5ATR8	Putative Unc104-like kinesin	TCDM_07835	Trypanosoma cruzi Dm28c	0	1
Q92636	Protein FAN	NSMAF FAN	Homo sapiens (human)	0	1
B6KB88	non-specific serine/threonine protein kinase	BN1205_075890	Toxoplasma gondii VEG	0	1
A0A2I3BPW0	Protein NDRG2 (Fragment)	Ndrg2	Mus musculus (house mouse)	0	1
P41240	Tyrosine-protein kinase CSK	CSK	Homo sapiens (human)	0	1
Q4QRB4	Tubulin beta-3 chain	Tubb3	Rattus norvegicus (Norway rat)	0	1
P04247	Myoglobin	Mb	Mus musculus (house mouse)	0	1
Q7TQ70	Fibrinogen alpha chain	Fga	Rattus norvegicus (Norway rat)	0	1
Q15528	Mediator of RNA polymerase II transcription subunit 22	MED22 SURF5	Homo sapiens (human)	2	1
P56282	DNA polymerase epsilon subunit 2	POLE2 DPE2	Homo sapiens (human)	1	1
A0A125YKP3	GPI transamidase subunit PIG-U protein	BN1205_028320	Toxoplasma gondii VEG	0	1
Q14209	Transcription factor E2F2	E2F2	Homo sapiens (human)	1	1
Q4U4S6	Xin actin-binding repeat-containing protein 2	Xirp2 Cmya3 Xin2	Mus musculus (house mouse)	4	1

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