"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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2010 | 0 | 1 | 1 |
| 2011 | 1 | 3 | 4 |
| 2012 | 2 | 1 | 3 |
| 2014 | 0 | 1 | 1 |
| 2015 | 1 | 1 | 2 |
| 2016 | 0 | 1 | 1 |
| 2017 | 0 | 1 | 1 |
| 2018 | 0 | 2 | 2 |
| 2019 | 2 | 4 | 6 |
| 2020 | 2 | 0 | 2 |
| 2021 | 0 | 3 | 3 |
| 2022 | 0 | 2 | 2 |
| 2024 | 0 | 2 | 2 |
| 2026 | 1 | 1 | 2 |
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Below are the most recent publications written about "INDEL Mutation" by people in Profiles.
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Genome-wide association study of INDELs identified four novel susceptibility loci associated with lung cancer risk. Int J Cancer. 2020 05 15; 146(10):2855-2864.
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A multi-task convolutional deep neural network for variant calling in single molecule sequencing. Nat Commun. 2019 03 01; 10(1):998.
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Megabase Length Hypermutation Accompanies Human Structural Variation at 17p11.2. Cell. 2019 03 07; 176(6):1310-1324.e10.
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De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome. Genome Med. 2019 02 28; 11(1):12.
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Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathies. Genet Med. 2019 03; 21(3):663-675.
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Spatial heterogeneity in medulloblastoma. Nat Genet. 2017 May; 49(5):780-788.
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Association between DBH 19bp insertion/deletion polymorphism and cognition in schizophrenia with and without tardive dyskinesia. Schizophr Res. 2017 04; 182:104-109.
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Association between D?H 5'-insertion/deletion polymorphism and cognition in patients with chronic schizophrenia. J Clin Psychiatry. 2016 Mar; 77(3):379-85.
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The genetic heterogeneity and mutational burden of engineered melanomas in zebrafish models. Genome Biol. 2013; 14(10):R113.
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Genomic landscape of non-small cell lung cancer in smokers and never-smokers. Cell. 2012 Sep 14; 150(6):1121-34.