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 **16526 - 16550** 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
P13639	Elongation factor 2	EEF2 EF2	Homo sapiens (human)	5	3
P21675	Transcription initiation factor TFIID subunit 1	TAF1 BA2R CCG1 CCGS TAF2A	Homo sapiens (human)	2	3
P48745	CCN family member 3	CCN3 IGFBP9 NOV NOVH	Homo sapiens (human)	9	3
Q15393	Splicing factor 3B subunit 3	SF3B3 KIAA0017 SAP130	Homo sapiens (human)	4	3
Q76FK4	Nucleolar protein 8	NOL8 C9orf34 NOP132	Homo sapiens (human)	2	3
Q9BY84	Dual specificity protein phosphatase 16	DUSP16 KIAA1700 MKP7	Homo sapiens (human)	2	3
Q11203	CMP-N-acetylneuraminate-beta-1,4-galactoside alpha-2,3-sialyltransferase	ST3GAL3 SIAT6	Homo sapiens (human)	3	3	Unverricht-Lundborg syndrome West syndrome agnosia amyotrophic lateral sclerosis attention deficit hyperactivity disorder autosomal recessive intellectual developmental disorder 12 autosomal recessive intellectual developmental disorder bipolar disorder blepharospasm brain cancer breast cancer breast carcinoma cancer cerebral degeneration cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma choreatic disease congenital disorder of glycosylation depressive disorder developmental and epileptic encephalopathy 15 developmental coordination disorder diabetes mellitus dysthymic disorder dystonia early infantile epileptic encephalopathy early myoclonic encephalopathy embryoma epilepsy focal epilepsy focal hand dystonia hepatocellular carcinoma influenza intellectual disability learning disability lingual-facial-buccal dyskinesia liver cancer major depressive disorder melancholic depression microcephaly neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia pancreatic adenocarcinoma partial motor epilepsy progressive muscular atrophy prostate cancer prostate carcinoma pterygium schizophrenia stereotypic movement disorder stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 type 2 diabetes mellitus visual epilepsy
Q5JU85	IQ motif and SEC7 domain-containing protein 2	IQSEC2 KIAA0522	Homo sapiens (human)	2	3
Q2KHR3	Glutamine and serine-rich protein 1	QSER1	Homo sapiens (human)	40	3
O95858	Tetraspanin-15	TSPAN15 NET7 TM4SF15	Homo sapiens (human)	3	3
Q13449	Limbic system-associated membrane protein	LSAMP IGLON3 LAMP	Homo sapiens (human)	9	3
Q8NBR0	Tumor protein p53-inducible protein 13	TP53I13 DSCP1	Homo sapiens (human)	9	3
O75592	E3 ubiquitin-protein ligase MYCBP2	MYCBP2 KIAA0916 PAM	Homo sapiens (human)	8	3
P07998	Ribonuclease pancreatic	RNASE1 RIB1 RNS1	Homo sapiens (human)	3	3
Q13336	Urea transporter 1	SLC14A1 HUT11 JK RACH1 UT1 UTE	Homo sapiens (human)	2	3
P60174	Triosephosphate isomerase	TPI1 TPI	Homo sapiens (human)	2	3	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 Behcet's disease Chagas disease Creutzfeldt-Jakob disease Ebola hemorrhagic fever Goodpasture syndrome Japanese encephalitis Pick's disease Reye syndrome Takayasu's arteritis adenocarcinoma adenoma adult respiratory distress syndrome allergic asthma alternating hemiplegia of childhood arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy aseptic meningitis asthma atherosclerosis atopic dermatitis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autonomic neuropathy bipolar disorder blastomycosis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiomyopathy central nervous system cancer central nervous system disease cerebral degeneration cholecystitis cholecystolithiasis choledocholithiasis cholelithiasis chronic fatigue syndrome chronic myeloid leukemia colorectal cancer colorectal carcinoma congenital hemolytic anemia congenital nonspherocytic hemolytic anemia congestive heart failure coronary artery disease cribriform carcinoma deafness-dystonia-optic neuronopathy syndrome dementia dengue disease dermatitis diaphragm disease diarrhea disease of metabolism dystonia embryoma encephalitis encephalomyelitis endomyocardial fibrosis epilepsy esophagus squamous cell carcinoma exanthem familial hypertrophic cardiomyopathy familial periodic paralysis favism giant cell glioblastoma giardiasis glioblastoma gliosarcoma granular cell carcinoma granulomatosis with polyangiitis head and neck cancer head and neck squamous cell carcinoma hemoglobinopathy hemolytic anemia hepatocellular carcinoma hereditary elliptocytosis high grade glioma hypertrophic cardiomyopathy immune system disease inherited metabolic disorder intellectual disability intrinsic asthma kwashiorkor large intestine cancer learning disability leech infestation lingual-facial-buccal dyskinesia liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma malignant pleural mesothelioma marasmus melanoma microsporidiosis mixed glioma multiple sclerosis myelitis myiasis myopathy nervous system disease neuroblastoma neuromuscular disease neuropathy newborn respiratory distress syndrome nodular goiter normocytic anemia nutrition disease ocular hypertension osteoarthritis osteochondritis dissecans osteoporosis papillary adenocarcinoma papillary renal cell carcinoma paracoccidioidomycosis peripheral nervous system disease periventricular leukomalacia pleurisy polyarteritis nodosa polyneuropathy progressive supranuclear palsy proliferative type fibrocystic change of breast protein-energy malnutrition reflex sympathetic dystrophy rheumatoid arthritis schizophrenia scleroderma skin melanoma squamous cell carcinoma stomach cancer stomach carcinoma systemic lupus erythematosus systemic scleroderma thyroid gland papillary carcinoma tongue squamous cell carcinoma toxoplasmosis triosephosphate isomerase deficiency trypanosomiasis tuberculosis tubular adenocarcinoma uveal melanoma viral infectious disease viral meningitis visual epilepsy yellow fever
Q9Y2B4	TP53-target gene 5 protein	TP53TG5 C20orf10	Homo sapiens (human)	1	3
P49755	Transmembrane emp24 domain-containing protein 10	TMED10 TMP21	Homo sapiens (human)	6	3
Q5T7N3	KN motif and ankyrin repeat domain-containing protein 4	KANK4 ANKRD38	Homo sapiens (human)	3	3
Q15629	Translocating chain-associated membrane protein 1	TRAM1 TRAM	Homo sapiens (human)	2	3
Q9NZC9	SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A-like protein 1	SMARCAL1 HARP	Homo sapiens (human)	2	3
Q08629	Testican-1	SPOCK1 SPOCK TIC1 TICN1	Homo sapiens (human)	9	3
P22891	Vitamin K-dependent protein Z	PROZ	Homo sapiens (human)	7	3
Q9H324	A disintegrin and metalloproteinase with thrombospondin motifs 10	ADAMTS10	Homo sapiens (human)	7	3
O14974	Protein phosphatase 1 regulatory subunit 12A	PPP1R12A MBS MYPT1	Homo sapiens (human)	59	3

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