GlyCosmos Portal

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Displaying entries **119601 - 119625** 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
Q91897	Fibroblast growth factor receptor	fgfr1.L E59 X1FGFR XFGFR-1 bfgfr cek fgfr-1 fgfr1 fgfr1-a fgfr1-b fgfr1.S flg flt-2 flt2 kal2 ogd x1fgfr xfgfr1	Xenopus laevis (African clawed frog)	8	0
A0A6J2LQK7	Fibroblast growth factor receptor	FGFR2	Phyllostomus discolor (pale spear-nosed bat)	8	0
Q86XN7	Proline and serine-rich protein 1	PROSER1 C13orf23 KIAA2032	Homo sapiens (human)	8	1
A0A2K6EKX8	Fibroblast growth factor receptor	FGFR1	Propithecus coquereli (Coquerel's sifaka)	8	0
Q8BJD1	Inter-alpha-trypsin inhibitor heavy chain H5	Itih5	Mus musculus (house mouse)	8	6
O70513	Galectin-3-binding protein	Lgals3bp	Rattus norvegicus (Norway rat)	8	0
A0A7K4RPT7	Fibroblast growth factor receptor 2 (Fragment)	Fgfr2	Columbina picui (picui ground-dove)	8	0
A0A5N4CGI3	Fibroblast growth factor receptor	Cadr_000026450	Camelus dromedarius (Arabian camel)	8	0
A0A1U8BFM4	Fibroblast growth factor receptor	Fgfr1	Mesocricetus auratus (golden hamster)	8	0
Q9BUN1	Protein MENT	MENT C1orf56	Homo sapiens (human)	8	4
A0A2K6L1U8	Fibroblast growth factor receptor	FGFR1	Rhinopithecus bieti (black snub-nosed monkey)	8	0
Q90275	Cadherin-2	cdh2 pac	Danio rerio (zebrafish)	8	0
A0A1A8DSP8	Fibroblast growth factor receptor	FGFR2	Nothobranchius kadleci	8	0
A0A7K7IMG5	Fibroblast growth factor receptor 1 (Fragment)	Fgfr1	Loxia curvirostra	8	0
Q54DA4	Putative potassium transport protein DDB_G0292412	DDB_G0292412	Dictyostelium discoideum	8	0
A0A7K9EWF3	Fibroblast growth factor receptor 1 (Fragment)	Fgfr1	Baryphthengus martii	8	0
A0A1S3FN18	Fibroblast growth factor receptor	Fgfr2	Dipodomys ordii (Ord's kangaroo rat)	8	0
A0A2K5Y6T6	Fibroblast growth factor receptor	FGFR1	Mandrillus leucophaeus (drill)	8	0
Q68Y56	Toll-like receptor 4	TLR4	Sus scrofa (pig)	8	0
A0A383ZEG2	Fibroblast growth factor receptor	FGFR2	Balaenoptera acutorostrata scammoni	8	0
P04062	Lysosomal acid glucosylceramidase	GBA1 GBA GC GLUC	Homo sapiens (human)	8	33	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 B-cell lymphoma Burkitt lymphoma Canavan 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 Cogan syndrome DiGeorge syndrome Fabry disease Gaucher's disease perinatal lethal Gaucher's disease type I Gaucher's disease type II Gaucher's disease type III Gaucher's disease type IIIC Gaucher's disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Lafora disease Langerhans-cell histiocytosis Laron syndrome Lewy body dementia Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease type C1 Niemann-Pick disease type C2 Niemann-Pick disease PCWH syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 2 Parkinson's disease 4 Parkinson's disease Pick's disease REM sleep behavior disorder Reye syndrome Sjogren-Larsson syndrome Tay-Sachs disease Unverricht-Lundborg syndrome West Nile fever Wolman disease abdominal obesity-metabolic syndrome 1 achondroplasia acquired hyperkeratosis actinic keratosis adult lymphoma agenesis of the corpus callosum with peripheral neuropathy agnosia alternating hemiplegia of childhood amyotrophic lateral sclerosis anemia arthritis arthropathy atypical Gaucher's disease due to saposin c deficiency autonomic neuropathy autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis autosomal recessive osteopetrosis 7 blepharospasm brain disease cancer cardiac arrest central nervous system disease central nervous system lymphoma cerebral degeneration childhood lymphoma chylomicron retention disease communicating hydrocephalus congestive heart failure dementia dentatorubral-pallidoluysian atrophy depressive disorder developmental coordination disorder diffuse interstitial keratitis diffuse large B-cell lymphoma dissociated nystagmus dysthymic disorder dystonia early myoclonic encephalopathy ectropion embryoma endometriosis of uterus endometriosis esotropia essential hypertension essential tremor female stress incontinence fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome focal hand dystonia follicular lymphoma glucose intolerance hemopericardium hepatitis B hepatopulmonary syndrome hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hydrocephalus hypertension hypomyelinating leukodystrophy 2 hypomyelinating leukodystrophy 3 hypomyelinating leukodystrophy 4 hypomyelinating leukodystrophy 6 hypomyelinating leukodystrophy 9 ichthyosis interstitial lung disease intracranial aneurysm keratosis follicularis late onset Parkinson's disease leukoencephalopathy with vanishing white matter leukopenia lingual-facial-buccal dyskinesia lipid storage disease liver cirrhosis lymphoma lysosomal storage disease macrocytic anemia major depressive disorder melancholic depression metachromatic leukodystrophy microcephaly mitral valve stenosis mongolian spot monocular esotropia motor peripheral neuropathy movement disease multiple myeloma nervous system disease neuroblastoma neurodegenerative disease neurotic disorder non-Hodgkin lymphoma obsolete congenital ichthyosiform erythroderma obsolete constipation obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia obsolete ymphosarcoma obstructive hydrocephalus ophthalmoplegia osteoarthritis osteonecrosis osteopetrosis osteosclerosis pancytopenia pathologic nystagmus pericardial effusion placental insufficiency polyhydramnios prediabetes syndrome primary pulmonary hypertension progressive muscular atrophy progressive myoclonus epilepsy 4 progressive myoclonus epilepsy progressive supranuclear palsy proteinuria pseudoxanthoma elasticum reticulosarcoma schizophrenia seborrheic keratosis secondary Parkinson disease senile degeneration of brain sensorineural hearing loss skin disease speech disorder sphingolipidosis spontaneous ocular nystagmus thrombocytopenia velocardiofacial syndrome
A0A6J2A980	Fibroblast growth factor receptor	FGFR1	Acinonyx jubatus (cheetah)	8	0
A0A6P8RAA0	Fibroblast growth factor receptor	FGFR1	Geotrypetes seraphini	8	0
Q05BC3	Echinoderm microtubule-associated protein-like 1	Eml1	Mus musculus (house mouse)	8	1
O89335	Lectin-like protein EP153R	Pret-069	African swine fever virus tick/South Africa/Pretoriuskop Pr4/1996	8	0

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