Insertion (genetics)
In genetics, an insertion (also called an insertion mutation) is the addition of one or more nucleotide base pairs into a DNA sequence. This can often happen in microsatellite regions due to the DNA polymerase slipping. Insertions can be anywhere in size from one base pair incorrectly inserted into a DNA sequence to a section of one chromosome inserted into another. The mechanism of the smallest single base insertion mutations is believed to be through base-pair separation between the template and primer strands followed by non-neighbor base stacking, which can occur locally within the DNA polymerase active site. On a chromosome level, an insertion refers to the insertion of a larger sequence into a chromosome. This can happen due to unequal crossover during meiosis.
Wikipage disambiguates
Wikipage redirect
5′ flanking regionANNOVARASPM (gene)Adaptive evolution in the human genome1,2-dimethoxyethaanAmfloraBFASTCLCN5Cancer syndromeCarcinogenesisCat coat geneticsCell-free fetal DNAChromosomal crossoverChromosome abnormalityCoding regionComparative genomics1,2-dimethoxyethaanComputational phylogeneticsCongenital mirror movement disorderCraig VenterCre-Lox recombinationCytogenetic notationDNADeletion (genetics)DysfibrinogenemiaDysosteosclerosisEnd-sequence profilingEvolving digital ecological networkFrameshift mutationGATA2GATA2 deficiencyGLUT1Gap penaltyGene expansionGene insertionGenetic codeGenetic insertionGenetic insertionsGenetically modified virusGenome-wide association study
Link from a Wikipage to another Wikipage
primaryTopic
Insertion (genetics)
In genetics, an insertion (also called an insertion mutation) is the addition of one or more nucleotide base pairs into a DNA sequence. This can often happen in microsatellite regions due to the DNA polymerase slipping. Insertions can be anywhere in size from one base pair incorrectly inserted into a DNA sequence to a section of one chromosome inserted into another. The mechanism of the smallest single base insertion mutations is believed to be through base-pair separation between the template and primer strands followed by non-neighbor base stacking, which can occur locally within the DNA polymerase active site. On a chromosome level, an insertion refers to the insertion of a larger sequence into a chromosome. This can happen due to unequal crossover during meiosis.
has abstract
En genética, una inserción (ta ...... clase separada de mutaciones.
@es
In genetics, an insertion (als ...... a separate class of mutations.
@en
Insercja (interkalacja) – najc ...... od miejsca insercji począwszy.
@pl
Insertie is een toevoeging van ...... rtie van een andere sequentie.
@nl
L'insertion est une mutation g ...... cytoplasmique après épissage).
@fr
Uma inserção genética é a adiç ...... ons de transcrição e tradução.
@pt
Инсерция (от англ. insertion — ...... рушений индели (англ. indels).
@ru
في علم الوراثة، الغرز أو طفرة ...... من كروموسوم إلى كروموسوم آخر.
@ar
插入(英語:Insertion)是指一個或多個核苷酸鹼基對插 ...... 插入另一條染色體,常發生在減數分裂時,染色體發生互換的時候。
@zh
Wikipage page ID
page length (characters) of wiki page
Wikipage revision ID
994,982,154
Link from a Wikipage to another Wikipage
wikiPageUsesTemplate
subject
hypernym
comment
En genética, una inserción (ta ...... a la inserción de una secuenc
@es
In genetics, an insertion (als ...... qual crossover during meiosis.
@en
Insercja (interkalacja) – najc ...... od miejsca insercji począwszy.
@pl
Insertie is een toevoeging van ...... rtie van een andere sequentie.
@nl
L'insertion est une mutation g ...... r lors d'un enjambement inégal
@fr
Uma inserção genética é a adiç ...... nto desigual durante a meiose.
@pt
Инсерция (от англ. insertion — ...... рушений индели (англ. indels).
@ru
في علم الوراثة، الغرز أو طفرة ...... من كروموسوم إلى كروموسوم آخر.
@ar
插入(英語:Insertion)是指一個或多個核苷酸鹼基對插 ...... 插入另一條染色體,常發生在減數分裂時,染色體發生互換的時候。
@zh
label
Inserción (genética)
@es
Insercja
@pl
Insertie (chromosomen)
@nl
Insertion (Genetik)
@de
Insertion (genetics)
@en
Insertion (génétique)
@fr
Inserção (genética)
@pt
Инсерция
@ru
غرز (وراثة)
@ar
插入 (遺傳學)
@zh