"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.
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".
Below are MeSH descriptors whose meaning is more specific than "INDEL Mutation".
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.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "INDEL Mutation" by people in Profiles.
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Simultaneous Gene Excision and Integration by Dual-Guide CRISPR-Cas9. Methods Mol Biol. 2021; 2307:69-83.