INDEL Mutation [mutace INDEL]

topical
17
Terms

INDEL mutace
inzerční/deleční mutace

 

INDELs Mutation
Insertion-Deletion Mutation
Insertions-Deletions Mutation

Persistent link   https://www.medvik.cz/link/D054643
Definition

A mutation named with the blend of insertion and deletion. It refers to a length difference between two ALLELES where it is unknowable if the difference was originally caused by a SEQUENCE INSERTION or by a SEQUENCE DELETION. If the number of nucleotides in the insertion/deletion is not divisible by three, and it occurs in a protein coding region, it is also a FRAMESHIFT MUTATION.

DUI
D054643 MeSH Browser
CUI
M0506591
History note
2008
Public note
2008

G Phenomena and Processes
G05.365.590 Mutation 5 029
G05.365.590.029 Allelic Imbalance 2
G05.365.590.060 Base Pair Mismatch 14
G05.365.590.175 Chromosome Aberrations 1 578
G05.365.590.195 Codon, Nonsense 52
G05.365.590.220 DNA Repeat Expansion 7
G05.365.590.265 Frameshift Mutation 47
G05.365.590.288 Gain of Function Mutation 18
G05.365.590.310 Gene Amplification 334
G05.365.590.320 Gene Duplication 65
G05.365.590.335 Genomic Instability 88
G05.365.590.350 Germ-Line Mutation 202
G05.365.590.500 INDEL Mutation 17
G05.365.590.538 Loss of Function Mutation 13
G05.365.590.575 Mutagenesis, Insertional 56
G05.365.590.594 Mutation Accumulation 3
G05.365.590.612 Mutation Rate 18
G05.365.590.650 Mutation, Missense 216
G05.365.590.675 Point Mutation 246
G05.365.590.762 Sequence Deletion 104
G05.365.590.770 Sequence Inversion 2
G05.365.590.803 Silent Mutation 2
G05.365.590.835 Suppression, Genetic 29
G05.558 Mutagenesis 276
G05.558.315 Gene Amplification 334
G05.558.320 Gene Duplication 65
G05.558.370 INDEL Mutation 17
G05.558.800 Sequence Deletion 104
G05.558.805 Sequence Inversion 2
G05.558.835 Suppression, Genetic 29
G05.558.860 Translocation, Genetic 343