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About:
Mutation
An Entity of Type:
Thing
,
from Named Graph:
http://dbpedia.org
,
within Data Space:
dbpedia.org
Change of the nucleotide sequence of the genome of an organism
Property
Value
dbo:
description
biologie
(nl)
生物やウイルスがもつ遺伝物質の質的・量的変化
(ja)
зміна генотипу, що передається у спадок
(uk)
Breyting á röð kirna í erfðamengi
(is)
dauerhafte Erbgutveränderung
(de)
förändring i cellens genetiska material
(sv)
genetická změna
(cs)
изменение генотипа, передаваемое по наследству
(ru)
muutos eliön perimäaineksessa
(fi)
perubahan urutan nukleotida genom suatu organisme
(in)
skokowe zmiany materiału genetycznego
(pl)
sprememba zaporedja nukleotidov v genomu organizma
(sl)
canvi en la seqüència d'un nucleòtid o en l'organització de l'ADN d'un ésser viu
(ca)
sự biến đổi trình tự nucleotide trong hệ gene sinh vật
(vi)
cambiamento nella sequenza dei nucleotidi nel genoma di un organismo
(it)
spontán változás a genom nukleotid szekvenciájában
(hu)
cambio en la secuencia de un nucleótido o en la organización del ADN de un ser vivo
(es)
mudanças na sequência dos nucleotídeos do material genético de um organismo
(pt)
change of the nucleotide sequence of the genome of an organism
(en)
ændring i en celles arvemateriale
(da)
canlının genomu içindeki DNA ya da RNA diziliminde meydana gelen kalıcı değişmeler
(tr)
שינוי בגנום
(iw)
تغييرات الجينوم
(ar)
基因突变
(zh)
유전정보가 기록된 DNA 분자가 여러가지 요인에 의하여 원본과 달라지는 것
(ko)
modification aléatoire de l'information génétique dans une cellule ou un virus
(fr)
dbo:
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wikiPageExternalLink
http://grenada.lumc.nl/LSDB_list/lsdbs/AR
https://mutalyzer.nl/
http://www.bbc.co.uk/programmes/b008drvm
https://web.stanford.edu/group/hopes/cgi-bin/hopes_test/all-about-mutations/
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Mutace
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Mutacio
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돌연변이
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Mutação
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Mutatie (biologie)
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Mutacja
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Мутація
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Мутация
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突变
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dbr
:Gracility
dbr
:ITD
dbr
:Identity_by_type
dbr
:List_of_X-Men_comics
dbr
:Ageing
dbr
:Arsène_Lupin
dbr
:Charlotte_Auerbach
dbr
:DDT
dbr
:Diffusion-limited_enzyme
dbr
:Fat-tailed_gerbil
dbr
:Haplogroup
dbr
:Haplotype
dbr
:Hypercycle_(chemistry)
dbr
:Luria–Delbrück_experiment
dbr
:Muscular_dystrophy
dbr
:Mutagenesis
dbr
:Octopus_minor
dbr
:Quasispecies_model
dbr
:Rett_syndrome
dbr
:Titin
dbr
:Warburg_effect_(oncology)
dbr
:Warburg_hypothesis
dbr
:Aramon_(grape)
dbr
:Archaeogenetics
dbr
:Atypical_teratoid_rhabdoid_tumor
dbr
:Cladogenesis
dbr
:Coactivator_(genetics)
dbr
:Macroevolution
dbr
:Menkes_disease
dbr
:Newton's_parakeet
dbr
:Terret_blanc
dbr
:The_Batman_(TV_series)
dbr
:Vestigiality
dbr
:Microsatellite
dbr
:Wheat
dbr
:Aicardi–Goutières_syndrome
dbr
:Androgen_receptor
dbr
:DNA_glycosylase
dbr
:Dominant_white
dbr
:Dopamine_receptor
dbr
:Dystrophin
dbr
:Estrogen_receptor
dbr
:Ethyl_methanesulfonate
dbr
:Exome
dbr
:Flight_feather
dbr
:Gap_gene
dbr
:Hereditary_hyperbilirubinemia
dbr
:Hexachlorocyclopentadiene
dbr
:Isopentenyl-diphosphate_delta_isomerase
dbr
:Isozyme
dbr
:Methyltransferase
dbr
:Mupirocin
dbr
:Mycolic_acid
dbr
:Neuropeptide_Y
dbr
:Nonsteroidal_antiandrogen
dbr
:PTEN_(gene)
dbr
:P_element
dbr
:Polycyclic_aromatic_hydrocarbon
dbr
:Propionyl-CoA_carboxylase
dbr
:Psoralen
dbr
:Ryanodine_receptor
dbr
:Sterol_O-acyltransferase
dbr
:TAAR1
dbr
:Transcription_factor
dbr
:Transferase
dbr
:Type_II_topoisomerase
dbr
:Von_Willebrand_factor
dbr
:Down_feather
dbr
:Fibroadenoma
dbr
:Myelodysplastic_syndrome
dbr
:Neurofilament
dbr
:Point_accepted_mutation
dbr
:Ampelography
dbr
:Cat_anatomy
dbr
:Complete_androgen_insensitivity_syndrome
dbr
:El_Topo
dbr
:War_on_cancer
dbr
:Cis-regulatory_element
dbr
:Coffin–Lowry_syndrome
dbr
:Cohen_syndrome
dbr
:Haplodiploidy
dbr
:History_of_life
dbr
:Joubert_syndrome
dbr
:Molecular-weight_size_marker
dbr
:Diastrophic_dysplasia
dbr
:Giant_axonal_neuropathy
dbr
:Nielluccio
dbr
:X-linked_myotubular_myopathy
dbr
:Nuclear_Device_(The_Wizard_of_Aus)
dbr
:Chris_J._Leaver
dbr
:Chromium_toxicity
dbr
:Cis_AB
dbr
:Kumquat
dbr
:Cranio-lenticulo-sutural_dysplasia
dbr
:Crested_(duck_breed)
dbr
:Crustacean_cardioactive_peptide
dbr
:Cubivore:_Survival_of_the_Fittest
dbr
:Production_of_antibiotics
dbr
:Shine–Dalgarno_sequence
dbr
:Fountain_of_Dreams
dbr
:Splice_site_mutation
dbr
:Plant_evolution
dbr
:Karen_Vousden
dbr
:Kataegis
dbr
:Astronautilia
dbr
:List_of_biophysicists
dbr
:List_of_fictional_diseases
dbr
:Macular_hypoplasia
dbr
:Major_histocompatibility_complex_and_sexual_selection
dbr
:Male_breast_cancer
dbr
:Malpuech_facial_clefting_syndrome
dbr
:Mammary-type_myofibroblastoma
dbr
:Trinucleotide_repeat_expansion
dbr
:It's_a_Disaster
dbr
:Developmental_bias
dbr
:Epstein–Barr_virus–associated_lymphoproliferative_diseases
dbr
:C9orf72
dbr
:Dmitry_Zhukov
dbr
:Insulated_neighborhood
dbr
:Sadaf_Farooqi
dbr
:Variant_of_uncertain_significance
dbr
:Natura_non_facit_saltus
dbr
:Cancer_pharmacogenomics
dbr
:Peter_Parker_(The_Amazing_Spider-Man_film_series)
dbr
:Viltolarsen
dbr
:Plácido_Navas_Lloret
dbr
:DNA_end_resection
dbr
:Phenol_sulfur_transferase_deficiency
dbr
:SARS-CoV-2_Alpha_variant
dbr
:Transfusion-dependent_anemia
dbr
:Urinary_cell-free_DNA
dbr
:Variants_of_SARS-CoV-2
dbr
:Fruit_flies_in_space
dbr
:Soft_selective_sweep
dbr
:Genetic_purging
dbr
:Position-effect_variegation
dbr
:Huntingtin
dbr
:Coalescent_theory
dbr
:Dual_inheritance_theory
dbr
:Evolution_strategy
dbr
:Fixation_(population_genetics)
dbr
:Chloroplast_DNA
dbr
:Intergenic_region
dbr
:Acquired_characteristic
dbr
:Adaptive_mutation
dbr
:Chimeric_gene
dbr
:Axenic
dbr
:Jackson–Weiss_syndrome
dbr
:Jeffrey_Flier
dbr
:Robustness_(evolution)
dbr
:Cancer_Genome_Project
dbr
:Mesoblastic_nephroma
dbr
:22q11.2_distal_deletion_syndrome
dbr
:Central_nervous_system_cavernous_hemangioma
dbr
:Hepatitis_E_virus_cis-reactive_element
dbr
:Information_gain_(decision_tree)
dbr
:List_of_The_Seven_Deadly_Sins_characters
dbr
:Phosphomimetics
dbr
:Sequence_space_(evolution)
dbr
:C2orf81
dbr
:Ccdc60
dbr
:MIPOL1
dbr
:SLC46A3
dbr
:Glucagon_receptor
dbr
:Saltation_(biology)
dbr
:Index_of_health_articles
dbr
:Replicator_equation
dbr
:Genetic_hitchhiking
dbr
:Corticotropin-releasing_hormone_receptor_1
dbr
:Crick,_Brenner_et_al._experiment
dbr
:Ka/Ks_ratio
dbr
:MonoMAC
dbr
:Formal_linguistics
dbr
:ALMS1
dbr
:Biology
dbr
:Cat
dbr
:Chernobyl_disaster
dbr
:Chicken
dbr
:Computer_virus
dbr
:Crohn's_disease
dbr
:Evolution
dbr
:Immune_system
dbr
:Language
dbr
:Linux
dbr
:Lion
dbr
:Love
dbr
:Meme
dbr
:Radium
dbr
:Angelman_syndrome
dbr
:Angiogenesis
dbr
:Caffeine
dbr
:Christina_Applegate
dbr
:Fancy_rat
dbr
:Genetic_disorder
dbr
:Hereditary_spherocytosis
dbr
:J._B._S._Haldane
dbr
:List_of_cat_body-type_mutations
dbr
:Medical_genetics
dbr
:P53
dbr
:Pelagic_cormorant
dbr
:Pheochromocytoma
dbr
:Social_selection
dbr
:Sumgait
dbr
:Trichorrhexis_invaginata
dbr
:Black_Hole_(comics)
dbr
:Chromium(III)_picolinate
dbr
:Doctorfish_tang
dbr
:Industrial_ecology
dbr
:Lipoprotein_lipase_deficiency
dbr
:Mothra_(film)
dbr
:Radioresistance
dbr
:Undifferentiated_pleomorphic_sarcoma
dbr
:Vampire_Bats_(film)
dbr
:White_lion
dbr
:Argininosuccinic_aciduria
dbr
:Catecholaminergic_polymorphic_ventricular_tachycardia
dbr
:Insertion_(genetics)
dbr
:Jaagsiekte_sheep_retrovirus
dbr
:Bramley_apple
dbr
:Channelopathy
dbr
:Microcephalin
dbr
:Occupational_cancer
dbr
:Outline_of_biology
dbr
:The_Voyage_that_Shook_the_World
dbr
:Trégorrois_Breton_dialect
dbr
:Dino_Island
dbr
:El-Fish
dbr
:Ipecac_Recordings_discography
dbr
:Machado–Joseph_disease
dbr
:Homeotic_gene
dbr
:Mutationism
dbr
:Mycoplasma_genitalium
dbr
:Neurofibromatosis_type_II
dbr
:Persistent_Müllerian_duct_syndrome
dbr
:Progressive_disease
dbr
:Duane-radial_ray_syndrome
dbr
:List_of_banana_cultivars
dbr
:Oculocutaneous_albinism
dbr
:Spinal_and_bulbar_muscular_atrophy
dbr
:Gene_polymorphism
dbr
:Titano
dbr
:Autophosphorylation
dbr
:Body_horror
dbr
:Ornithine_aminotransferase_deficiency
dbr
:Coding_region
dbr
:Hypoprothrombinemia
dbr
:Indeterminism
dbr
:List_of_Marvel_Comics_teams_and_organizations
dbr
:Factor_V
dbr
:LDL_receptor
dbr
:Trudy_Mackay
dbr
:Allele-specific_oligonucleotide
dbr
:Allochronic_speciation
dbr
:Alopecia_contractures_dwarfism_intellectual_disability_syndrome
dbr
:Alveolar_capillary_dysplasia
dbr
:Amelanism
dbr
:Aminoacylase
dbr
:Anne_Stone_(academic)
dbr
:Proteasome
dbr
:Panayiotopoulos_syndrome
dbr
:Pandemia
dbr
:Parastremmatic_dwarfism
dbr
:Paternal_age_effect
dbr
:Pathogenic_Escherichia_coli
dbr
:Pancreatic_neuroendocrine_tumor
dbr
:Resistance_Database_Initiative
dbr
:Resistance_mutation_(virology)
dbr
:Semen_cryopreservation
dbr
:United_States_Academic_Decathlon
dbr
:The_Boneyard
dbr
:The_Colours_of_Animals
dbr
:The_Family_That_Walks_on_All_Fours
dbr
:The_Genetical_Theory_of_Natural_Selection
dbr
:Crooked_Trees
dbr
:Tracheoesophageal_septum
dbr
:Trametinib
dbr
:Transgenerational_epigenetic_inheritance
dbr
:Transmission_and_infection_of_H5N1
dbr
:Transposon_mutagenesis
dbr
:Transposons_as_a_genetic_tool
dbr
:Tricho–dento–osseous_syndrome
dbr
:Tripedalism
dbr
:Tubby_protein
dbr
:TxpA-RatA_toxin-antitoxin_system
dbr
:Cellular_senescence
dbr
:Holocarboxylase_synthetase
dbr
:Nonsyndromic_deafness
dbr
:Sunturion
dbr
:Dougherty_(apple)
is
dbp:
causes
of
dbr
:Van_De_Berghe_Dequeker_syndrome
dbr
:Ornithine_transcarbamylase_deficiency
dbr
:Split_hand_split_foot-nystagmus_syndrome
dbr
:Klippel–Feil_syndrome
dbr
:Williams–Campbell_syndrome
dbr
:Congenital_insensitivity_to_pain_with_anhidrosis
dbr
:Congenital_amegakaryocytic_thrombocytopenia
dbr
:Autosomal_recessive_bestrophinopathy
dbr
:Spondyloepimetaphyseal_dysplasia-short_limb-abnormal_calcification_syndrome
dbr
:Du_Pan_syndrome
dbr
:Intellectual_disability-spasticity-ectrodactyly_syndrome
dbr
:Barth_syndrome
dbr
:Schneckenbecken_dysplasia
dbr
:Salt_and_pepper_syndrome
dbr
:Dilated_cardiomyopathy_with_ataxia_syndrome
dbr
:Autosomal_dominant_leukodystrophy_with_autonomic_disease
dbr
:Lubani_Al_Saleh_Teebi_syndrome
dbr
:Familial_natural_short_sleep
dbr
:Al_Gazali_Sabrinathan_Nair_syndrome
dbr
:Muscular_atrophy-ataxia-retinitis_pigmentosa-diabetes_mellitus_syndrome
dbr
:Marsili_syndrome
dbr
:Goldmann–Favre_syndrome
dbr
:Chudley–Mccullough_syndrome
dbr
:Corneal_dystrophy-perceptive_deafness_syndrome
dbr
:Pai_syndrome
dbr
:Autosomal_recessive_isolated_ectopia_lentis
dbr
:Bainbridge–Ropers_syndrome
dbr
:Camptodactyly,_tall_stature,_and_hearing_loss_syndrome
dbr
:Severe_intellectual_disability-progressive_spastic_diplegia_syndrome
dbr
:Absence_of_fingerprints-congenital_milia_syndrome
dbr
:Mandibulofacial_dysostosis-microcephaly_syndrome
dbr
:Proud_syndrome
dbr
:X-linked_cone-rod_dystrophy,_type_1
dbr
:Familial_thoracic_aortic_aneurysm_and_aortic_dissection
dbr
:IVIC_syndrome
dbr
:Dejerine–Sottas_disease
dbr
:North_Carolina_macular_dystrophy
dbr
:Familial_opposable_triphalangeal_thumbs_duplication
dbr
:Absence_deformity_of_leg-cataract_syndrome
dbr
:Blepharophimosis_intellectual_disability_syndromes
dbr
:Boucher-Neuhäuser_syndrome
dbr
:Calvarial_doughnut_lesions-bone_fragility_syndrome
dbr
:Collins–Pope_syndrome
dbr
:Czech_dysplasia,_metatarsal_type
dbr
:Distichiasis,_congenital_heart_defects_and_mixed_peripheral_vascular_anomalies
dbr
:Familial_multiple_cafe-au-lait_spots
dbr
:Familial_nasal_acilia
dbr
:Feigenbaum-Bergeron-Richardson_syndrome
dbr
:Hamanishi_Ueba_Tsuji_syndrome
dbr
:Heart-hand_syndrome,_Slovenian_type
dbr
:Iris_hypoplasia_with_glaucoma
dbr
:Microcephaly_deafness_syndrome
dbr
:Oculopharyngodistal_myopathy
dbr
:Ostravik-Lindemann-Solberg_syndrome
dbr
:Otofaciocervical_syndrome
dbr
:Pierre_Robin_sequence-faciodigital_anomaly_syndrome
dbr
:Rhizomelic_dysplasia,_scoliosis,_and_retinitis_pigmentosa
dbr
:SOFT_syndrome
dbr
:Scalp_defects-postaxial_polydactyly_syndrome
dbr
:Short-limb_skeletal_dysplasia_with_severe_combined_immunodeficiency
dbr
:Spondyloenchondrodysplasia
dbr
:Spondylometaphyseal_dysplasia_with_cone-rod_dystrophy
dbr
:Sudden_infant_death_with_dysgenesis_of_the_testes_syndrome
dbr
:Syndactyly-nystagmus_syndrome_due_to_2q31.1_microduplication
dbr
:Tucker_syndrome
dbr
:Ventricular_extrasystoles_with_syncopa...s-perodactyly-Robin_sequence_syndrome
dbr
:Wolfram-like_syndrome
dbr
:Wormian_bone-multiple_fractures-dentin...mperfecta-skeletal_dysplasia_syndrome
dbr
:X-linked_complicated_corpus_callosum_dysgenesis
dbr
:Y-linked_deafness,_type_1
dbr
:SLC35A1-CDG
dbr
:Metacarpal_synostosis
dbr
:Polymetatarsia
dbr
:Retinal_cone_dystrophy_3B
dbr
:Autosomal_dominant_cerebellar_ataxia,_deafness,_and_narcolepsy
dbr
:X-linked_Charcot–Marie–Tooth_disease
dbr
:Gollop-Wolfgang_complex
dbr
:Megalocornea-intellectual_disability_syndrome
dbr
:Ectrodactyly_with_tibia_aplasia/hypoplasia
dbr
:Autosomal_dominant_Charcot–Marie–Tooth_disease_type_2_with_giant_axons
dbr
:Osteopathia_striata_with_cranial_sclerosis
dbr
:Spastic_paraplegia_6
dbr
:Autosomal_dominant_intellectual_disabi...al_anomalies-cardiac_defects_syndrome
dbr
:GRIN2B-related_neurodevelopmental_disorder
dbr
:Angel-shaped_phalango-epiphyseal_dysplasia
dbr
:Al-Gazali-Donnai-Mueller_syndrome
dbr
:Autism_with_port-wine_stain_syndrome
dbr
:Boudhina-Yedes-Khiari_syndrome
dbr
:Camptodactyly-taurinuria_syndrome
dbr
:Congenital_muscular_dystrophy-infantile_cataract-hypogonadism_syndrome
dbr
:Dwarfism,_low-birth-weight_type_with_unresponsiveness_to_growth_hormone
dbr
:Hirschsprung's_disease-type_D_brachydactyly_syndrome
dbr
:Isolated_hyperCKemia
dbr
:MacDermot–Winter_syndrome
dbr
:Meacham_syndrome
dbr
:Microcephalic_primordial_dwarfism,_Montreal_type
dbr
:Microcornea,_glaucoma,_and_absent_frontal_sinuses
dbr
:Olivopontocerebellar_atrophy-deafness_syndrome
dbr
:Palmoplantar_keratoderma_with_deafness
dbr
:Say-Field-Coldwell_syndrome
dbr
:Splenogonadal_fusion-limb_defects-micrognathia_syndrome
dbr
:Tel_Hashomer_camptodactyly_syndrome
dbr
:Thai_symphalangism_syndrome
dbr
:Thumb_stiffness-brachydactyly-intellectual_disability_syndrome
dbr
:Triphalangeal_thumbs-brachyectrodactyly_syndrome
dbr
:Viljoen–Kallis–Voges_syndrome
dbr
:Weyer's_ulnar_ray/oligodactyly_syndrome
dbr
:PRICKLE1-related_progressive_myoclonus_epilepsy_with_ataxia
dbr
:Multiple_congenital_anomalies-hypotonia-seizures_syndrome
dbr
:Infantile_cerebellar_retinal_degeneration
dbr
:Cerebro-costo-mandibular_syndrome
dbr
:CAPOS_syndrome
dbr
:Autosomal_dominant_partial_epilepsy_with_auditory_features
dbr
:Cousin–Walbraum–Cegarra_syndrome
dbr
:Juvenile-onset_dystonia
is
dbp:
content
of
dbr
:Glossary_of_botanical_terms
is
dbp:
fields
of
dbr
:Shri_Mohan_Jain
is
dbp:
scope
of
dbr
:The_Monarch_Initiative
is
dbp:
species
of
dbr
:Peter_Parker_(The_Amazing_Spider-Man_film_series)
dbr
:Julie_Power
dbr
:Answer_(comics)
dbr
:Jackpot_(character)
dbr
:Alternative_versions_of_Spider-Man
dbr
:Viper_(Madame_Hydra)
dbr
:Darkdevil
dbr
:Aero_(manhua)
dbr
:Delroy_Garrett
dbr
:Power_Man_(Victor_Alvarez)
dbr
:3-D_Man
dbr
:Captain_Ultra
dbr
:Spider-Man_(Takuya_Yamashiro)
dbr
:Firebird_(Marvel_Comics)
dbr
:Spider-Man_(Pavitr_Prabhakar)
dbr
:Baron_Von_Blitzschlag
dbr
:Doctor_Minerva
dbr
:White_Tiger_(Angela_del_Toro)
dbr
:Peter_Parker_(Sam_Raimi_film_series)
is
gold:
hypernym
of
dbr
:Cis_AB
dbr
:Splice_site_mutation
dbr
:Trinucleotide_repeat_expansion
dbr
:White_lion
dbr
:ΔF508
dbr
:Nonsense_mutation
dbr
:Deletion_(genetics)
dbr
:Transition_(genetics)
dbr
:Frameshift_mutation
dbr
:Suppressor_mutation
dbr
:Point_mutation
dbr
:White_(mutation)
dbr
:Pure_hair-nail_type_ectodermal_dysplasia
dbr
:Lutino_cockatiel
dbr
:Pied_cockatiel
dbr
:Missense_mutation
dbr
:Wijcik_McIntosh
dbr
:White-faced_cockatiel
dbr
:BRCA_mutation
dbr
:Consonant_gradation
dbr
:C957T
dbr
:Nonsynonymous_substitution
dbr
:Hypodiploid_acute_lymphoblastic_leukemia
dbr
:V600E
dbr
:T790M
dbr
:Nonsense_suppressor
dbr
:Resistance_mutation
dbr
:Pseudodeficiency_alleles
dbr
:Behavior_mutation
is
owl:
differentFrom
of
dbr
:Nutation
is
foaf:
primaryTopic
of
wikipedia-en
:Mutation
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