GlyCosmos Portal

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GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
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The O-GlcNAc Database	June 3, 2024
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Displaying entries **15026 - 15050** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
Q9H0S4	Probable ATP-dependent RNA helicase DDX47	DDX47	Homo sapiens (human)	0	1
O00193	Small acidic protein	SMAP C11orf58	Homo sapiens (human)	2	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
Q7Z5P4	17-beta-hydroxysteroid dehydrogenase 13	HSD17B13 SCDR9 SDR16C3	Homo sapiens (human)	1	1
Q13670	Putative postmeiotic segregation increased 2-like protein 11	PMS2P11 PMS2L11 PMSR6	Homo sapiens (human)	0	1
Q13882	Protein-tyrosine kinase 6	PTK6 BRK	Homo sapiens (human)	0	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
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
Q9BVV7	Mitochondrial import inner membrane translocase subunit Tim21	TIMM21 C18orf55 TIM21	Homo sapiens (human)	2	1
Q9H3R5	Centromere protein H	CENPH ICEN35	Homo sapiens (human)	0	1
Q9NX65	Zinc finger and SCAN domain-containing protein 32	ZSCAN32 ZNF434	Homo sapiens (human)	0	1
P78545	ETS-related transcription factor Elf-3	ELF3 ERT ESX JEN	Homo sapiens (human)	0	1
Q9HCY8	Protein S100-A14	S100A14 S100A15	Homo sapiens (human)	0	1
Q15046	Lysine--tRNA ligase	KARS1 KARS KIAA0070	Homo sapiens (human)	2	1
Q9ULD8	Potassium voltage-gated channel subfamily H member 3	KCNH3 KIAA1282	Homo sapiens (human)	4	1
P17098	Zinc finger protein 8	ZNF8	Homo sapiens (human)	0	1
Q6P2C8	Mediator of RNA polymerase II transcription subunit 27	MED27 CRSP34 CRSP8	Homo sapiens (human)	0	1
Q13415	Origin recognition complex subunit 1	ORC1 ORC1L PARC1	Homo sapiens (human)	0	1
Q9NRG9	Aladin	AAAS ADRACALA	Homo sapiens (human)	2	1
Q9Y2V7	Conserved oligomeric Golgi complex subunit 6	COG6 KIAA1134	Homo sapiens (human)	2	1	Gilbert syndrome acquired hyperkeratosis allergic asthma anemia anhidrosis asthma bilirubin metabolic disorder blood coagulation disease cerebral degeneration cholestasis congenital disorder of glycosylation type II congenital disorder of glycosylation type IIl congenital disorder of glycosylation coronary artery disease dental caries dental enamel hypoplasia dentin caries developmental and epileptic encephalopathy 36 epilepsy gastroenteritis gastrointestinal system disease hydrocephalus hypohidrosis intellectual disability intestinal disease intrinsic asthma juvenile rheumatoid arthritis learning disability leiomyoma macrocytic anemia microcephaly myofibroma nonepidermolytic palmoplantar keratoderma palmoplantar keratosis pancytopenia parapsoriasis placental insufficiency primary biliary cholangitis primary immunodeficiency disease proctitis psoriasis pustulosis of palm and sole rheumatoid arthritis systemic lupus erythematosus thrombocytopenia uterine fibroid visual epilepsy
Q14151	Scaffold attachment factor B2	SAFB2 KIAA0138	Homo sapiens (human)	1	1

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