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 **122601 - 122625** 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
P83741	Serine/threonine-protein kinase WNK1	Wnk1 Hsn2 Prkwnk1	Mus musculus (house mouse)	44	2
P22303	Acetylcholinesterase	ACHE	Homo sapiens (human)	3	2	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 3 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Balo concentric sclerosis Chagas disease Clostridium difficile colitis Creutzfeldt-Jakob disease Duchenne muscular dystrophy Gamstorp-Wohlfart syndrome Gerstmann-Straussler-Scheinker syndrome Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Hirschsprung's disease Horner's syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease IGSF1 deficiency syndrome Japanese encephalitis Kawasaki disease Lafora disease Lambert-Eaton myasthenic syndrome Lewy body dementia Marfan syndrome Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Noonan syndrome 1 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Peutz-Jeghers syndrome Pick's disease Q fever Reye syndrome Schwartz-Jampel syndrome 1 Wilson-Turner syndrome abdominal obesity-metabolic syndrome 1 acoustic neuroma acute monocytic leukemia acute myeloid leukemia acute myocardial infarction acute stress disorder adrenoleukodystrophy adult medulloblastoma allergic asthma alternating hemiplegia of childhood amnestic disorder amphetamine abuse amyloidosis amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anaplastic astrocytoma anterior horn cell disease anxiety disorder arteriosclerotic cardiovascular disease asthma atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome autonomic neuropathy 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 distal hereditary motor neuronopathy 1 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 bacterial sepsis bipolar disorder bladder carcinoma blood platelet disease brain cancer brain disease breast cancer breast carcinoma cancer cardiac arrest cardiovascular system disease carotid artery disease cauda equina neoplasm central nervous system disease central nervous system origin vertigo centronuclear myopathy X-linked centronuclear myopathy cerebellar ataxia cerebellar disease cerebral atherosclerosis cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease chancroid childhood cerebral astrocytoma childhood disintegrative disease childhood leukemia childhood medulloblastoma chromophobe renal cell carcinoma chronic kidney disease chronic monocytic leukemia chronic myelomonocytic leukemia chronic obstructive pulmonary disease clear cell renal cell carcinoma cognitive disorder collecting duct carcinoma colon cancer colonic benign neoplasm colonic pseudo-obstruction colorectal cancer colorectal carcinoma congenital hypothyroidism congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy congenital myasthenic syndrome 5 congenital myasthenic syndrome congenital myopathy 1A congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 congenital structural myopathy congestive heart failure contractures, pterygia, and spondylocarpotarsal fusion syndrome conversion disorder coronary artery disease coronary thrombosis cystic fibrosis dementia dengue disease depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis disease of metabolism dissociative amnesia dissociative disorder distal myopathy dysthymic disorder dystonia embryoma endocrine exophthalmos endometritis enophthalmos epilepsy episodic ataxia type 1 essential thrombocythemia facioscapulohumeral muscular dystrophy familial hyperlipidemia fibrillary astrocytoma fibromyalgia focal epilepsy frontotemporal dementia gallbladder disease gemistocytic astrocytoma generalized anxiety disorder glaucoma head and neck squamous cell carcinoma heart disease hemiplegia hepatocellular carcinoma high grade glioma hyperglycemia hypothyroidism idiopathic scoliosis immune system disease impotence inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease intellectual disability intracranial arteriosclerosis intrinsic asthma irritable bowel syndrome juvenile myelomonocytic leukemia juvenile pilocytic astrocytoma kidney cancer large intestine cancer laryngeal squamous cell carcinoma lateral sclerosis learning disability leptospirosis leukemia limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia liver cancer liver carcinoma liver cirrhosis liver disease lower respiratory tract disease lung benign neoplasm lung cancer lung non-small cell carcinoma lung small cell carcinoma lymphogranuloma venereum major depressive disorder malaria malignant astrocytoma medulloblastoma medullomyoblastoma megaconial type congenital muscular dystrophy melancholic depression melanoma melanotic medulloblastoma migraine morbid obesity motor neuron disease movement disease multiple epiphyseal dysplasia multiple sclerosis muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myasthenia gravis myelodysplastic syndrome myelomeningocele myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myositis myotonic dystrophy type 2 myxedema narcolepsy nasal cavity disease necrotizing ulcerative gingivitis nemaline myopathy nervous system disease neuroblastoma neurocirculatory asthenia neurodegenerative disease neurofibroma neuromuscular disease neuromuscular junction disease neurotic disorder nonpapillary renal cell carcinoma normocytic anemia nutmeg liver obesity 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 constipation obsolete exophthalmos obsolete melancholia obsolete ymphosarcoma oculopharyngeal muscular dystrophy orbital disease osteochondrodysplasia osteoporosis ovarian cancer overnutrition papillary adenocarcinoma papillary renal cell carcinoma paranasal sinus disease partial motor epilepsy perineurioma peripheral nerve sheath neoplasm peripheral nervous system neoplasm persian gulf syndrome phobic disorder pilocytic astrocytoma polydactyly premature ejaculation primary pulmonary hypertension prion disease progressive muscular atrophy prostate cancer prostate carcinoma protoplasmic astrocytoma psychologic dyspareunia psychotic disorder renal carcinoma renal cell carcinoma retrograde amnesia rigid spine muscular dystrophy 1 rippling muscle disease 2 sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder secondary Parkinson disease silent myocardial infarction situs inversus skin melanoma sleeping sickness spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spinal muscular atrophy sporadic breast cancer status epilepticus stomach cancer stomach carcinoma subacute delirium subependymal giant cell astrocytoma substance abuse substance-related disorder temporal arteritis teratocarcinoma tethered spinal cord syndrome thanatophoric dysplasia thrombocytopenia thyroid gland papillary carcinoma trypanosomiasis tuberous sclerosis type 2 diabetes mellitus typhus ulcerative colitis upper respiratory tract disease urinary bladder cancer varicose veins vascular dementia viral infectious disease visual epilepsy vitiligo von Hippel-Lindau disease yaws yellow fever
B2RQG2	PHD finger protein 3	Phf3	Mus musculus (house mouse)	1	2
P06745	Glucose-6-phosphate isomerase	Gpi Gpi1	Mus musculus (house mouse)	1	2
Q8WVM7	Cohesin subunit SA-1	STAG1 SA1 SCC3	Homo sapiens (human)	2	2
P38570	Integrin alpha-E	ITGAE	Homo sapiens (human)	11	2
Q96PQ5	Putative protein phosphatase inhibitor 2-like protein 1	PPP1R2P1	Homo sapiens (human)	2	2
P49848	Transcription initiation factor TFIID subunit 6	TAF6 TAF2E TAFII70	Homo sapiens (human)	19	2
Q9C099	Leucine-rich repeat and coiled-coil domain-containing protein 1	LRRCC1 CLERC KIAA1764	Homo sapiens (human)	2	2
Q9CXZ1	NADH dehydrogenase [ubiquinone] iron-sulfur protein 4, mitochondrial	Ndufs4	Mus musculus (house mouse)	1	2
Q8TEQ8	GPI ethanolamine phosphate transferase 3	PIGO	Homo sapiens (human)	4	2	Cogan syndrome Hirschsprung's disease Marfan syndrome Unverricht-Lundborg syndrome absence epilepsy blepharospasm capillary disease childhood absence epilepsy cleft palate colorectal cancer colorectal carcinoma craniosynostosis diffuse interstitial keratitis early myoclonic encephalopathy esotropia focal hand dystonia hereditary hemorrhagic telangiectasia hydronephrosis hyperopia imperforate anus intellectual disability isolated cleft palate large intestine cancer learning disability monocular esotropia nonepidermolytic palmoplantar keratoderma oligohydramnios palmoplantar keratosis scoliosis sensorineural hearing loss situs inversus syndromic X-linked intellectual disability 94 telangiectasis tuberous sclerosis visual epilepsy
O70400	PDZ and LIM domain protein 1	Pdlim1 Clim1	Mus musculus (house mouse)	8	2
O60675	Transcription factor MafK	MAFK	Homo sapiens (human)	12	2
P53994	Ras-related protein Rab-2A	Rab2a Rab2	Mus musculus (house mouse)	1	2
Q9UI26	Importin-11	IPO11 RANBP11	Homo sapiens (human)	1	2
Q9DBG3	AP-2 complex subunit beta	Ap2b1 Clapb1	Mus musculus (house mouse)	3	2
Q62009	Periostin	Postn Osf2	Mus musculus (house mouse)	1	2
Q03145	Ephrin type-A receptor 2	Epha2 Eck Myk2 Sek2	Mus musculus (house mouse)	2	2
O15547	P2X purinoceptor 6	P2RX6 P2RXL1 P2X6	Homo sapiens (human)	3	2
Q80U04	E3 ubiquitin-protein ligase Praja-2	Pja2 Kiaa0438 Rnf131	Mus musculus (house mouse)	1	2
O75157	TSC22 domain family protein 2	TSC22D2 KIAA0669 TILZ4	Homo sapiens (human)	9	2
P62750	Large ribosomal subunit protein uL23	RPL23A	Homo sapiens (human)	2	2
Q70Z35	Phosphatidylinositol 3,4,5-trisphosphate-dependent Rac exchanger 2 protein	PREX2 DEPDC2	Homo sapiens (human)	2	2
Q923U0	TOM1-like protein 1	Tom1l1 Srcasm	Mus musculus (house mouse)	2	2
Q9ULM3	YEATS domain-containing protein 2	YEATS2 KIAA1197	Homo sapiens (human)	35	2

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