INDEL Mutation

"INDEL Mutation" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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.

Descriptor ID	D054643
MeSH Number(s)	G05.365.590.500 G05.558.370
Concept/Terms	INDEL Mutation INDEL Mutation INDEL Mutations Mutation, INDEL Mutations, INDEL Insertion-Deletion Mutation Insertion Deletion Mutation Insertion-Deletion Mutations Mutation, Insertion-Deletion Mutations, Insertion-Deletion

Below are MeSH descriptors whose meaning is more general than "INDEL Mutation".

Biological Sciences [G]
Genetic Phenomena [G05]
Genetic Variation [G05.365]
Mutation [G05.365.590]
INDEL Mutation [G05.365.590.500]
Mutagenesis [G05.558]
INDEL Mutation [G05.558.370]

Below are MeSH descriptors whose meaning is more specific than "INDEL Mutation".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "INDEL Mutation" by people in this website by year, and whether "INDEL Mutation" was a major or minor topic of these publications.

Bar chart showing 2 publications over 2 distinct years, with a maximum of 1 publications in 2015 and 2018

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
2015	0	1	1
2018	0	1	1