GlyCosmos Portal

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

Displaying entries **119251 - 119275** 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
A0A803TVY4	Fibroblast growth factor receptor	FGFR1	Anolis carolinensis (green anole)	8	0
Q8BG07	5'-3' exonuclease PLD4	Pld4	Mus musculus (house mouse)	8	6
A0A6P6QJF6	Fibroblast growth factor receptor	LOC113112374	Carassius auratus (goldfish)	8	0
A0A671L818	Fibroblast growth factor receptor	LOC107655670	Sinocyclocheilus anshuiensis	8	0
G5B5S0	Fibroblast growth factor receptor	GW7_16755	Heterocephalus glaber (naked mole-rat)	8	0
A0A5N3WMR9	Angiotensin-converting enzyme	FD754_007275	Muntiacus muntjak (muntjak)	8	0
A0A8C7ATN0	Fibroblast growth factor receptor	FGFR1	Neogale vison (American mink)	8	0
A0A1D8PS71	Phytase PHO112	PHO112	Candida albicans SC5314	8	0
A0A7E6DW92	Fibroblast growth factor receptor	FGFR2	Phyllostomus discolor (pale spear-nosed bat)	8	0
A0A091E9I6	Fibroblast growth factor receptor 1 (Fragment)	N302_03452	Corvus brachyrhynchos (American crow)	8	0
A0A4D9EEK3	Fibroblast growth factor receptor	DR999_PMT07038	Platysternon megacephalum (big-headed turtle)	8	0
A0A3Q7T634	Fibroblast growth factor receptor	FGFR2	Vulpes vulpes (red fox)	8	0
A0A7L1Q088	Fibroblast growth factor receptor 1 (Fragment)	Fgfr1	Oriolus oriolus (Eurasian golden-oriole)	8	0
A0A8D0E205	Fibroblast growth factor receptor	FGFR1	Salvator merianae (Argentine black and white tegu)	8	0
A0A6J2DHJ2	Fibroblast growth factor receptor	FGFR1	Zalophus californianus (California sea lion)	8	0
A0A7K8U706	Fibroblast growth factor receptor 1 (Fragment)	Fgfr1	Oceanites oceanicus (Wilson's storm-petrel)	8	0
A0A9W3G9L9	Fibroblast growth factor receptor	FGFR1	Camelus bactrianus (Bactrian camel)	8	0
Q7FAZ3	G-type lectin S-receptor-like serine/threonine-protein kinase LECRK1	LECRK1	Oryza sativa Japonica Group (Japanese rice)	8	0
H2V7F6	Fibroblast growth factor receptor	fgfr2	Takifugu rubripes (torafugu)	8	0
Q9DR81	Hemagglutinin-esterase	HE	Bovine coronavirus strain Ontario	8	0
A0A671L7Y1	Fibroblast growth factor receptor	LOC107655670	Sinocyclocheilus anshuiensis	8	0
Q9Y286	Sialic acid-binding Ig-like lectin 7	SIGLEC7 AIRM1	Homo sapiens (human)	8	32	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 Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Guillain-Barre syndrome Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Marfan syndrome Miller Fisher syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome T-cell acute lymphoblastic leukemia Zollinger-Ellison syndrome acoustic neuroma acute biphenotypic leukemia acute leukemia acute myeloid leukemia adenosquamous carcinoma adult fibrosarcoma adult medulloblastoma agenesis of the corpus callosum with peripheral neuropathy allergic rhinitis alternating hemiplegia of childhood amyotrophic lateral sclerosis ankylosing spondylitis arthritis arthropathy atopic dermatitis atypical chronic myeloid leukemia, BCR-ABL1 negative autonomic neuropathy autosomal dominant familial periodic fever benign mesothelioma bipolar disorder bone marrow cancer brain stem infarction breast cancer breast carcinoma cancer cellular schwannoma central nervous system cancer central nervous system disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebral primitive neuroectodermal tumor cerebrovascular disease childhood medulloblastoma chordoma chronic lymphocytic leukemia chronic monocytic leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cone-rod dystrophy 2 cone-rod dystrophy delusional disorder depressive disorder dermatitis detrusor sphincter dyssynergia diabetes mellitus diabetic ketoacidosis dysthymic disorder eating disorder embryoma endometriosis of uterus endometriosis epilepsy esophagus squamous cell carcinoma familial combined hyperlipidemia familial hypercholesterolemia familial retinoblastoma fibrosarcoma gallbladder disease gangliocytoma ganglioneuroblastoma ganglioneuroma gastrinoma gastrointestinal system cancer gliosarcoma glomerulonephritis hepatitis hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 high grade glioma hyperglycemia hyperinsulinism kidney disease large intestine cancer laryngeal carcinoma larynx cancer leukemia liver disease lymphoid leukemia major depressive disorder malignant mesothelioma malignant peripheral nerve sheath tumor medulloblastoma medulloepithelioma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma melanotic neurilemmoma microphthalmia mixed glioma motor peripheral neuropathy myeloid leukemia myeloproliferative neoplasm nephritis nervous system disease neurilemmoma neuroblastoma neurodegenerative disease neuroectodermal tumor neurotic disorder obsolete Matthew-Wood syndrome obsolete T-cell lymphoblastic leukemia/lymphoma obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia osteoarthritis pancreatic ductal adenocarcinoma panic disorder paranoid schizophrenia plexiform schwannoma preretinal fibrosis progressive muscular atrophy prostate adenocarcinoma prostate cancer prostate carcinoma retinoblastoma rheumatoid arthritis rhinitis sick sinus syndrome situs inversus skin melanoma squamous cell carcinoma steatotic liver disease supratentorial primitive neuroectodermal tumor tendinitis tongue squamous cell carcinoma trilateral retinoblastoma tuberous sclerosis type 2 diabetes mellitus vasomotor rhinitis
P55317	Hepatocyte nuclear factor 3-alpha	FOXA1 HNF3A TCF3A	Homo sapiens (human)	8	1
A0A2K5XVG5	Fibroblast growth factor receptor	FGFR2	Mandrillus leucophaeus (drill)	8	0
P13806	Voltage-dependent calcium channel subunit alpha-2/delta-1	CACNA2D1 CACNL2A CCHL2A	Oryctolagus cuniculus (rabbit)	8	0

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