GlyCosmos Portal

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The O-GlcNAc Database	June 3, 2024
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Displaying entries **120551 - 120575** 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
V5BNS0	T-complex protein 1 subunit gamma	TCDM_05217	Trypanosoma cruzi Dm28c	0	1
P38833	Uncharacterized protein YHR127W	YHR127W	Saccharomyces cerevisiae S288C	4	1
Q6P9N1	Hyccin	Hycc1 Drctnnb1a Fam126a	Mus musculus (house mouse)	3	1
Q9UNZ5	Leydig cell tumor 10 kDa protein homolog	C19orf53	Homo sapiens (human)	0	1
Q9UL16	Cilia- and flagella-associated protein 45	CFAP45 CCDC19 NESG1	Homo sapiens (human)	0	1
P85973	Purine nucleoside phosphorylase	Pnp Np	Rattus norvegicus (Norway rat)	0	1
Q7Z5P4	17-beta-hydroxysteroid dehydrogenase 13	HSD17B13 SCDR9 SDR16C3	Homo sapiens (human)	1	1
V5DFU6	mannose-6-phosphate isomerase	TCDM_05062	Trypanosoma cruzi Dm28c	0	1
Q9VCR7	Cystinosin homolog	CG17119	Drosophila melanogaster (fruit fly)	2	1
Q13670	Putative postmeiotic segregation increased 2-like protein 11	PMS2P11 PMS2L11 PMSR6	Homo sapiens (human)	0	1
Q4DDS8	DNA-(apurinic or apyrimidinic site) endonuclease	Tc00.1047053509901.170	Trypanosoma cruzi strain CL Brener	0	1
Q923D2	Flavin reductase (NADPH)	Blvrb Scan	Mus musculus (house mouse)	0	1
Q13882	Protein-tyrosine kinase 6	PTK6 BRK	Homo sapiens (human)	0	1
V5BQQ6	AMP-activated protein kinase glycogen-binding domain-containing protein	TCDM_02643	Trypanosoma cruzi Dm28c	0	1
P32259	Mediator of RNA polymerase II transcription subunit 16	SIN4 BEL2 GAL22 MED16 RYE1 SDI3 SSF5 SSN4 TSF3	Saccharomyces cerevisiae S288C	4	1
Q9NVI1	Fanconi anemia group I protein	FANCI KIAA1794	Homo sapiens (human)	0	1
O43426	Synaptojanin-1	SYNJ1 KIAA0910	Homo sapiens (human)	7	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 Creutzfeldt-Jakob disease Down syndrome Duchenne muscular dystrophy Joubert syndrome 1 Joubert syndrome Laron syndrome Parkinson's disease 19A Parkinson's disease 1 Parkinson's disease 20 Parkinson's disease 23 Parkinson's disease 2 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Unverricht-Lundborg syndrome achondroplasia amnestic disorder amyotrophic lateral sclerosis anodontia attention deficit hyperactivity disorder autistic disorder autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bipolar disorder blepharospasm blindness borderline personality disorder brain disease cerebral degeneration cone-rod dystrophy congenital muscular dystrophy congenital nystagmus congenital ptosis dementia developmental and epileptic encephalopathy 1 developmental and epileptic encephalopathy 53 dissociated nystagmus distal myopathy dystonia early infantile epileptic encephalopathy early myoclonic encephalopathy early-onset Parkinson's disease epilepsy esophagitis facioscapulohumeral muscular dystrophy focal hand dystonia fundus albipunctatus gastroesophageal reflux disease giant cell glioblastoma glioblastoma high grade glioma intellectual disability intermittent explosive disorder isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia locked-in syndrome microcephaly muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 neuroblastoma neurodegenerative disease obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete infantile epileptic encephalopathy oculopharyngeal muscular dystrophy optic atrophy pathologic nystagmus peptic esophagitis progressive muscular atrophy ptosis quadriplegia retinal degeneration retinitis pigmentosa retrograde amnesia rhabdomyosarcoma rippling muscle disease 2 scoliosis secondary Parkinson disease spontaneous ocular nystagmus status epilepticus tauopathy tooth agenesis visual epilepsy
Q8K363	ATP-dependent RNA helicase DDX18	Ddx18	Mus musculus (house mouse)	1	1
A8MWD9	Putative small nuclear ribonucleoprotein G-like protein 15	SNRPGP15	Homo sapiens (human)	1	1
Q9P0X4	Voltage-dependent T-type calcium channel subunit alpha-1I	CACNA1I KIAA1120	Homo sapiens (human)	7	1
Q9BYM8	RanBP-type and C3HC4-type zinc finger-containing protein 1	RBCK1 C20orf18 RNF54 UBCE7IP3 XAP3 XAP4	Homo sapiens (human)	0	1
K2M5Q0	Transmembrane protein	MOQ_005974	Trypanosoma cruzi marinkellei	0	1
Q9Z2D6	Methyl-CpG-binding protein 2	Mecp2	Mus musculus (house mouse)	5	1
Q9BVV7	Mitochondrial import inner membrane translocase subunit Tim21	TIMM21 C18orf55 TIM21	Homo sapiens (human)	2	1
P43565	Serine/threonine-protein kinase RIM15	RIM15 TAK1	Saccharomyces cerevisiae S288C	3	1

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