GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **3976 - 4000** 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
Q17RC7	Exocyst complex component 3-like protein 4	EXOC3L4 C14orf73	Homo sapiens (human)	1	1
Q96A65	Exocyst complex component 4	EXOC4 KIAA1699 SEC8 SEC8L1	Homo sapiens (human)	1	2
O00471	Exocyst complex component 5	EXOC5 SEC10 SEC10L1	Homo sapiens (human)	0	1
Q9UPT5	Exocyst complex component 7	EXOC7 EXO70 KIAA1067	Homo sapiens (human)	0	1
Q8IYI6	Exocyst complex component 8	EXOC8	Homo sapiens (human)	0	1
Q9Y3B2	Exosome complex component CSL4	EXOSC1 CSL4	Homo sapiens (human)	0	1
Q01780	Exosome complex component 10	EXOSC10 PMSCL PMSCL2 RRP6	Homo sapiens (human)	2	2
Q13868	Exosome complex component RRP4	EXOSC2 RRP4	Homo sapiens (human)	0	1
Q9NQT5	Exosome complex component RRP40	EXOSC3 RRP40	Homo sapiens (human)	0	1
Q9NPD3	Exosome complex component RRP41	EXOSC4 RRP41 SKI6	Homo sapiens (human)	0	1
Q9NQT4	Exosome complex component RRP46	EXOSC5 CML28 RRP46	Homo sapiens (human)	1	2
Q5RKV6	Exosome complex component MTR3	EXOSC6 MTR3	Homo sapiens (human)	0	1
Q15024	Exosome complex component RRP42	EXOSC7 KIAA0116 RRP42	Homo sapiens (human)	0	1
Q96B26	Exosome complex component RRP43	EXOSC8 OIP2 RRP43	Homo sapiens (human)	1	2
Q06265	Exosome complex component RRP45	EXOSC9 PMSCL1	Homo sapiens (human)	0	1
Q8NEV8	Exophilin-5	EXPH5 KIAA0624 SLAC2B	Homo sapiens (human)	0	1
H7C1H6	Exostosin glycosyltransferase 1 (Fragment)	EXT1	Homo sapiens (human)	1	0
S5Y321	Exostosin (Fragment)	EXT1	Homo sapiens (human)	1	0
Q16394	Exostosin-1	EXT1	Homo sapiens (human)	2	1	Alzheimer's disease Cenani-Lenz syndactyly syndrome Cornelia de Lange syndrome 4 Cornelia de Lange syndrome Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Laron syndrome Legg-Calve-Perthes disease Lennox-Gastaut syndrome Leri-Weill dyschondrosteosis Maffucci syndrome Ollier disease Pick's disease Reye syndrome Ritter's disease Werner syndrome achondroplasia acute lymphoblastic leukemia adenocarcinoma adenoma adult acute lymphocytic leukemia anaplastic astrocytoma antisocial personality disorder arthritis arthropathy autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome bone cancer bone disease bone osteosarcoma breast cancer breast carcinoma cancer cartilage disease central nervous system cancer cerebral degeneration cervix uteri carcinoma in situ cherubism childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood leukemia chondroblastoma chondroma chondrosarcoma cleidocranial dysplasia clubfoot conduct disorder connective tissue disease cranial nerve disease cranial nerve palsy cribriform carcinoma cryoglobulinemia diabetes mellitus disease of mental health embryoma endometrial cancer endometrial carcinoma epilepsy exostosis familial hypercholesterolemia familial nephrotic syndrome fibrillary astrocytoma fibromyalgia frontotemporal dementia gallbladder disease gemistocytic astrocytoma gliosarcoma granular cell carcinoma head and neck squamous cell carcinoma hepatitis A hepatitis B hepatitis C hepatitis E hepatitis hepatocellular carcinoma hereditary multiple exostoses high grade glioma humeroradial synostosis hydrocephalus hyperostosis hypogonadism hypogonadotropic hypogonadism 7 with or without anosmia immune system disease intellectual disability juvenile myoclonic epilepsy juvenile pilocytic astrocytoma learning disability leukemia lipoid nephrosis liver cancer liver disease lupus nephritis malignant astrocytoma membranous glomerulonephritis metachondromatosis microcephaly mixed glioma mucopolysaccharidosis III mucopolysaccharidosis type IIIA multiple myeloma myositis nephrotic syndrome osteoarthritis osteonecrosis osteopoikilosis osteoporosis osteosarcoma periarthritis personality disorder pilocytic astrocytoma progeria protoplasmic astrocytoma psychotic disorder radioulnar synostosis rectal benign neoplasm rectum adenocarcinoma rectum cancer rheumatoid arthritis schizophrenia scoliosis spinal cord disease subependymal giant cell astrocytoma tendinitis thrombophilia trichorhinophalangeal syndrome type II tubular adenocarcinoma type 2 diabetes mellitus urinary tract obstruction uterine corpus cancer vasculitis vesicoureteral reflux visual epilepsy
Q93063	Exostosin-2	EXT2	Homo sapiens (human)	2	2	Alzheimer's disease Cenani-Lenz syndactyly syndrome Dent disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Laron syndrome Leri-Weill dyschondrosteosis Maffucci syndrome Marfan syndrome Ollier disease Pick's disease Reye syndrome achondroplasia adenosarcoma agnosia anemia arthritis arthropathy autoimmune disease autoimmune lymphoproliferative syndrome bone cancer bone disease bone osteosarcoma breast cancer breast carcinoma cancer cartilage disease cerebral degeneration cherubism chondrosarcoma cleidocranial dysplasia clubfoot congenital hypothyroidism congenital nystagmus connective tissue disease cranial nerve disease cranial nerve palsy craniosynostosis cryptorchidism developmental and epileptic encephalopathy 36 developmental coordination disorder diabetes mellitus diabetic ketoacidosis dissociated nystagmus epilepsy esophagitis essential hypertension exostosis familial hypercholesterolemia frontotemporal dementia gastroesophageal reflux disease hereditary multiple exostoses humeroradial synostosis hyperostosis hypertension hypertropia hypothyroidism immune system disease intellectual disability large intestine cancer learning disability lupus nephritis macrocytic anemia mechanical strabismus membranous glomerulonephritis metachondromatosis microcephaly mucopolysaccharidosis III mucopolysaccharidosis type IIIA myxedema nephroblastoma nonsyndromic congenital nail disorder 9 obsolete constipation ophthalmoplegia osteoarthritis osteonecrosis osteosarcoma parietal foramina pathologic nystagmus peptic esophagitis periarthritis radioulnar synostosis scoliosis situs inversus spontaneous ocular nystagmus stereotypic movement disorder strabismus tendinitis tuberous sclerosis type 2 diabetes mellitus ventricular septal defect visual epilepsy
Q92935	Exostosin-like 1	EXTL1 EXTL	Homo sapiens (human)	1	0	cancer embryoma neuroblastoma
Q9UBQ6	Exostosin-like 2	EXTL2 EXTR2	Homo sapiens (human)	1	0	autosomal dominant osteopetrosis 2 autosomal recessive osteopetrosis 7 cancer chronic kidney disease hereditary multiple exostoses mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIC mucopolysaccharidosis osteopetrosis osteosclerosis
O43909	Exostosin-like 3	EXTL3 EXTL1L EXTR1 KIAA0519	Homo sapiens (human)	10	5	MHC class II deficiency acute myeloid leukemia adenosine deaminase deficiency agnosia arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant osteopetrosis 2 autosomal recessive osteopetrosis 7 bacterial sepsis brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cherubism chondrodysplasia punctata ciliary body disease cocaine abuse cocaine dependence colorectal cancer colorectal carcinoma coronary artery disease developmental coordination disorder endometriosis of uterus endometriosis epithelioid sarcoma exostosis giant cell glioblastoma glioblastoma head and neck cancer head and neck squamous cell carcinoma hereditary multiple exostoses hypereosinophilic syndrome intellectual disability iris disease large intestine cancer learning disability liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphopenia morphine dependence mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIC mucopolysaccharidosis multiple epiphyseal dysplasia nutmeg liver osteochondrodysplasia osteopetrosis osteosclerosis panuveitis periarthritis pulmonary embolism sarcoma scoliosis secondary syphilis severe combined immunodeficiency spindle cell sarcoma tendinitis tuberculosis uveitis
O00167	Eyes absent homolog 2	EYA2 EAB1	Homo sapiens (human)	0	1
Q99504	Eyes absent homolog 3	EYA3	Homo sapiens (human)	5	3

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