Address
:
[go:
up one dir
,
main page
]
Include Form
Remove Scripts
Accept Cookies
Show Images
Show Referer
Rotate13
Base64
Strip Meta
Strip Title
Session Cookies
Browse using
OpenLink Faceted Browser
OpenLink Structured Data Editor
LodLive Browser
Formats
RDF:
N-Triples
N3
Turtle
JSON
XML
OData:
Atom
JSON
Microdata:
JSON
HTML
Embedded:
JSON
Turtle
Other:
CSV
JSON-LD
Faceted Browser
Sparql Endpoint
About:
Missense mutation
An Entity of Type:
Thing
,
from Named Graph:
http://dbpedia.org
,
within Data Space:
dbpedia.org
Genetic point mutation that results in an amino acid change in a protein
Property
Value
dbo:
description
геномда бір нуклеин негізінің алмасуымен байланысты пайда болған мутациялар
(kk)
mutació puntual genètica que dóna lloc a un canvi d’aminoàcids en una proteïna
(ca)
genetic point mutation that results in an amino acid change in a protein
(en)
dbo:
thumbnail
wiki-commons
:Special:FilePath/Missense_Mutation_Example.jpg?width=300
dbo:
wikiPageWikiLink
dbr
:Nonsynonymous_substitution
dbr
:Alanine
dbc
:Mutation
dbc
:Modification_of_genetic_information
dbr
:Thymine
dbr
:Arginine
dbr
:Nonsense_mutation
dbr
:Epidermolysis_bullosa
dbr
:Phenotype
dbr
:Glutamic_acid
dbr
:Superoxide_dismutase
dbr
:Valine
dbr
:Point_mutation
dbr
:Amino_acid
dbr
:Genetics
dbr
:Protein
dbr
:Leucine
dbr
:Guanine
dbr
:Asparagine
dbr
:Threonine
dbr
:Cancer
dbr
:Hemoglobin
dbr
:Serine
dbr
:Ka/Ks_ratio
dbr
:Missense_mRNA
dbr
:LMNA
dbr
:Nucleotide
dbr
:Stop_codon
dbr
:Synonymous_substitution
dbr
:Amyotrophic_lateral_sclerosis
dbr
:Salt_bridge_(protein)
dbr
:Mandibuloacral_dysplasia
dbr
:Codon
dbr
:Sickle-cell_disease
dbr
:Beta_chain
dbr
:Fast_parallel_proteolysis_(FASTpp)
dbr
:Progeria_syndrome
dbr
:File:Missense_Mutation_Example.jpg
dbr
:File:LMNA_protein_(1IFR)_mutation_R527L_PMID_22549407.png
dbp:
displayAuthors
6
(xsd:integer)
dbp:
nameListStyle
vanc
(en)
dbp:
wikiPageUsesTemplate
dbt
:Commons_category
dbt
:Reflist
dbt
:Mutation
dbt
:Cs1_config
dbt
:Short_description
dct:
subject
dbc
:Mutation
dbc
:Modification_of_genetic_information
gold:
hypernym
dbr
:Mutation
rdfs:
label
Missense mutation
(en)
طفرة مغلطة
(ar)
Mutació amb canvi de sentit
(ca)
Mutación con cambio de sentido
(es)
Mutation faux sens
(fr)
ミスセンス突然変異
(ja)
Mutacja zmiany sensu
(pl)
Mutação do Tipo Missense
(pt)
Миссенс-мутация
(ru)
Missense-mutation
(sv)
錯義突變
(zh)
owl:
sameAs
freebase
:Missense mutation
wikidata
:Missense mutation
dbpedia-fr
:Missense mutation
dbpedia-zh
:Missense mutation
dbpedia-ja
:Missense mutation
dbpedia-pt
:Missense mutation
dbpedia-he
:Missense mutation
dbpedia-da
:Missense mutation
dbpedia-es
:Missense mutation
dbpedia-fa
:Missense mutation
dbpedia-ru
:Missense mutation
dbpedia-sv
:Missense mutation
dbpedia-vi
:Missense mutation
dbpedia-pl
:Missense mutation
dbpedia-ca
:Missense mutation
dbpedia-ar
:Missense mutation
dbpedia-bs
:Missense mutation
dbpedia-fi
:Missense mutation
dbpedia-gl
:Missense mutation
dbpedia-kk
:Missense mutation
dbpedia-no
:Missense mutation
dbpedia-global
:Missense mutation
prov:
wasDerivedFrom
wikipedia-en
:Missense_mutation?oldid=1291654405&ns=0
foaf:
depiction
wiki-commons
:Special:FilePath/Point_mutations-en.png
wiki-commons
:Special:FilePath/Missense_Mutation_Example.jpg
wiki-commons
:Special:FilePath/Adenine-Thymine_tautomers.png
wiki-commons
:Special:FilePath/DNA_Repair_Mechanisms.png
wiki-commons
:Special:FilePath/LMNA_protein_(1IFR)_mutation_R527L_PMID_22549407.png
wiki-commons
:Special:FilePath/Phylogenetic_tree_of_SNP_variations.png
wiki-commons
:Special:FilePath/Sickle_cell_anemia.jpg
foaf:
isPrimaryTopicOf
wikipedia-en
:Missense_mutation
is
dbo:
wikiPageRedirects
of
dbr
:Missense
dbr
:Missense_mutations
dbr
:Missense_substitution
is
dbo:
wikiPageWikiLink
of
dbr
:Lujan–Fryns_syndrome
dbr
:Roussy–Lévy_syndrome
dbr
:Nonsynonymous_substitution
dbr
:Noggin_(protein)
dbr
:Prp8
dbr
:Familial_natural_short_sleep
dbr
:TOC1_(gene)
dbr
:Neurogenetics
dbr
:Kuru_(disease)
dbr
:Neural_crest
dbr
:Advanced_sleep_phase_disorder
dbr
:Noonan_syndrome_with_multiple_lentigines
dbr
:Dravet_syndrome
dbr
:Neoplasm
dbr
:Frameshift_mutation
dbr
:Pantothenate_kinase-associated_neurodegeneration
dbr
:Mitochondrial_DNA_depletion_syndrome
dbr
:Ocular_albinism_type_1
dbr
:Mutation_rate
dbr
:Silver_dapple_gene
dbr
:JUNQ_and_IPOD
dbr
:Neonatal_diabetes
dbr
:Neuroligin
dbr
:Index_of_genetics_articles
dbr
:Aldolase_A_deficiency
dbr
:1000_Genomes_Project
dbr
:Genetic_code
dbr
:Parastremmatic_dwarfism
dbr
:Adolescent_idiopathic_scoliosis
dbr
:Autosomal_dominant_intellectual_disabi...al_anomalies-cardiac_defects_syndrome
dbr
:CHAMP1-associated_intellectual_disability_syndrome
dbr
:Curry–Jones_syndrome
dbr
:FBXW7_neurodevelopmental_syndrome
dbr
:Hypodysfibrinogenemia
dbr
:Mandibulofacial_dysostosis-microcephaly_syndrome
dbr
:Meacham_syndrome
dbr
:Palmoplantar_keratoderma_with_deafness
dbr
:Pallid_bat
dbr
:Melanopsin
dbr
:Single-nucleotide_polymorphism
dbr
:Nonsense_mutation
dbr
:Waardenburg_syndrome
dbr
:CYLD_cutaneous_syndrome
dbr
:Champagne_gene
dbr
:Fainting_goat
dbr
:Dominant_white
dbr
:Silent_mutation
dbr
:Estrogen_insensitivity_syndrome
dbr
:Malpuech_facial_clefting_syndrome
dbr
:Mutant_protein
dbr
:Thromboxane_receptor
dbr
:UTP—glucose-1-phosphate_uridylyltransferase
dbr
:Sodium/glucose_cotransporter_1
dbr
:Niemann–Pick_disease
dbr
:Point_mutation
dbr
:Asinara_donkey
dbr
:Epoxygenase
dbr
:Benign_familial_neonatal_seizures
dbr
:Retinol_dehydrogenase
dbr
:DNA_repair
dbr
:Molecular_genetics
dbr
:Protein_biosynthesis
dbr
:Chestnut_(horse_color)
dbr
:Oculocutaneous_albinism_type_I
dbr
:Bilateral_frontoparietal_polymicrogyria
dbr
:D-bifunctional_protein_deficiency
dbr
:Cherubism
dbr
:Stargardt_disease
dbr
:Wiskott–Aldrich_syndrome
dbr
:Causes_of_Parkinson's_disease
dbr
:Ghosal_hematodiaphyseal_dysplasia
dbr
:Inborn_errors_of_carbohydrate_metabolism
dbr
:Index_of_molecular_biology_articles
dbr
:Gene
dbr
:Tay–Sachs_disease
dbr
:Smith–Lemli–Opitz_syndrome
dbr
:Co-receptor
dbr
:Birt–Hogg–Dubé_syndrome
dbr
:ASPM_(gene)
dbr
:Forward_genetics
dbr
:Abruzzo–Erickson_syndrome
dbr
:Acute_fatty_liver_of_pregnancy
dbr
:Progeroid_syndromes
dbr
:MT-ATP6
dbr
:Leukoencephalopathy_with_neuroaxonal_spheroids
dbr
:Coronavirus_nucleocapsid_protein
dbr
:Facial_infiltrating_lipomatosis
dbr
:Animal_model_of_schizophrenia
dbr
:Human_variability
dbr
:Albinism
dbr
:Glucose-6-phosphate_dehydrogenase
dbr
:Hereditary_haemochromatosis
dbr
:Primary_effusion_lymphoma
dbr
:Alternating_hemiplegia
dbr
:Chylomicron_retention_disease
dbr
:Johanson–Blizzard_syndrome
dbr
:Melanoma
dbr
:Carcinogenesis
dbr
:Mutation
dbr
:Dystonia
dbr
:Ribose-5-phosphate_isomerase
dbr
:New_Forest_pony
dbr
:Neurofibromatosis_type_II
dbr
:Pyruvate_kinase_deficiency
dbr
:Hereditary_sensory_and_autonomic_neuropathy_type_I
dbr
:DHHC_domain
dbr
:DNA_construct
dbr
:Northern_epilepsy_syndrome
dbr
:Cream_gene
dbr
:Hereditary_neuropathy_with_liability_to_pressure_palsy
dbr
:3-Hydroxy-3-methylglutaryl-CoA_lyase
dbr
:Variants_of_SARS-CoV-2
dbr
:Tennessee_Walking_Horse
dbr
:Congenital_myasthenic_syndrome
dbr
:Saethre–Chotzen_syndrome
dbr
:TRPA1
dbr
:P-type_calcium_channel
dbr
:Hypoprothrombinemia
dbr
:Ka/Ks_ratio
dbr
:Missense_mRNA
dbr
:Spinal_muscular_atrophy_with_progressive_myoclonic_epilepsy
dbr
:ACTC1
dbr
:COX6B1
dbr
:CSPG4
dbr
:TIMM8A
dbr
:Cranio-lenticulo-sutural_dysplasia
dbr
:Lenz–Majewski_syndrome
dbr
:Stop_codon
dbr
:Equine_coat_color_genetics
dbr
:Inverted_repeat
dbr
:Juvenile_myoclonic_epilepsy
dbr
:Antley–Bixler_syndrome
dbr
:Hay–Wells_syndrome
dbr
:Centronuclear_myopathy
dbr
:Crouzon_syndrome
dbr
:Causes_of_autism
dbr
:Alagille_syndrome
dbr
:Catecholaminergic_polymorphic_ventricular_tachycardia
dbr
:Van_der_Woude_syndrome
dbr
:Neuronal_ceroid_lipofuscinosis
dbr
:Cancer_epigenetics
dbr
:Complex_vertebral_malformation
dbr
:Megacolon
dbr
:Morgan_horse
dbr
:Omenn_syndrome
dbr
:Coding_region
dbr
:Laminopathy
dbr
:Björnstad_syndrome
dbr
:Synonymous_substitution
dbr
:NPAS2
dbr
:Steroidogenic_factor_1
dbr
:Parkin_(protein)
dbr
:Aromatase_deficiency
dbr
:Congenital_distal_spinal_muscular_atrophy
dbr
:Hydrolethalus_syndrome
dbr
:Ichthyosis_prematurity_syndrome
dbr
:Recombination_signal_sequences
dbr
:Rs16891982
dbr
:Helical_growth
dbr
:Dysfibrinogenemia
dbr
:H3K27me3
dbr
:Amino_acid_replacement
dbr
:Endocrine_therapy_resistance_in_breast_cancer
dbr
:Diane_Lipscombe
dbr
:Sex-linked_barring
dbr
:L1_syndrome
dbr
:Microphthalmia,_syndromic_12_(MCOPS12)
dbr
:Vel_blood_group
dbr
:Sid_blood_group_system
dbr
:Ubiquitin-activating_enzyme
dbr
:C18orf63
dbr
:C2orf81
dbr
:C6orf58
dbr
:CCDC130
dbr
:COX14
dbr
:CXorf66
dbr
:Dehydrodolichyl_diphosphate_synthase
dbr
:FAM151A
dbr
:GIPC3
dbr
:LOXL3
dbr
:LSMEM1
dbr
:MASTL
dbr
:Proline-rich_protein_21
dbr
:Protein_wntless_homolog
dbr
:SDHAF1
dbr
:SLC46A3
dbr
:TMEM155
dbr
:UQCC3
dbr
:WWC2
dbr
:Junior_blood_group_system
dbr
:Animal_models_of_Parkinson's_disease
dbr
:Adenosine_deaminase_2_deficiency
dbr
:Calvarial_doughnut_lesions-bone_fragility_syndrome
dbr
:Multisystemic_smooth_muscle_dysfunction_syndrome
dbr
:Leigh_syndrome,_French_Canadian_type
dbr
:Blue_cone_monochromacy
dbr
:Nav1.7
dbr
:BRCA1
dbr
:ABHD12
dbr
:Bestrophin_1
dbr
:FARS2
dbr
:GABRB3
dbr
:GBP2
dbr
:Glycogenin-1
dbr
:Granulin
dbr
:HAND2
dbr
:HIPK2
dbr
:Hydroxyacyl-Coenzyme_A_dehydrogenase
dbr
:KAT6A
dbr
:KCNC1
dbr
:MAFB_(gene)
dbr
:MYL7
dbr
:NDUFAF1
dbr
:NDUFAF7
dbr
:P4HB
dbr
:PITX1
dbr
:PKM2
dbr
:PLD3
dbr
:POLD1
dbr
:PSMB8
dbr
:PSTPIP2
dbr
:RAB7A
dbr
:RAPSN
dbr
:Retinaldehyde-binding_protein_1
dbr
:SCN1A
dbr
:SCO2
dbr
:SUCLA2
dbr
:SURF1
dbr
:SYNGAP1-related_intellectual_disability
dbr
:TBX15
dbr
:Transmembrane_protein_251
dbr
:WNK4
dbr
:YME1L1
dbr
:ZNF337
dbr
:ADAR
dbr
:CLCN5
dbr
:Collagen,_type_VII,_alpha_1
dbr
:ISCU
dbr
:Spongy_degeneration_of_the_central_nervous_system
dbr
:Coronavirus_membrane_protein
dbr
:ORF1ab
dbr
:Angiotensin-converting_enzyme_2
dbr
:CHEK2
dbr
:Cell–cell_recognition
dbr
:ETV6
dbr
:Fibroblast_growth_factor_receptor_3
dbr
:Glucagon_receptor
dbr
:Keratin_5
dbr
:Norepinephrine_transporter
dbr
:SLC22A5
dbr
:Sodium-chloride_symporter
dbr
:TRPV6
dbr
:Neotenic_complex_syndrome
dbr
:Hemoglobin_M_disease
dbr
:DNA_methylation_in_cancer
dbr
:Congenital_hypofibrinogenemia
dbr
:Microlissencephaly
dbr
:Dysosteosclerosis
dbr
:Tyrosinase
dbr
:GRIN_disorder
dbr
:Zaki_syndrome
dbr
:Glossary_of_genetics
dbr
:Marsili_syndrome
dbr
:Arginine_finger
dbr
:Escherichia_coli_NC101
dbr
:HK1
dbr
:Ethylene_as_a_plant_hormone
dbr
:O-6-methylguanine-DNA_methyltransferase
dbr
:Glossary_of_genetics_(M−Z)
dbr
:CX3CR1
dbr
:Cerebral_autosomal_recessive_arteriopa...ical_infarcts_and_leukoencephalopathy
dbr
:Missense
dbr
:Missense_mutations
dbr
:Missense_substitution
dbr
:No-SCAR_(Scarless_Cas9_Assisted_Recombineering)_Genome_Editing
is
foaf:
primaryTopic
of
wikipedia-en
:Missense_mutation
This content was extracted from
Wikipedia
and is licensed under the
Creative Commons Attribution-ShareAlike 4.0 International