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INDEL Mutation - Genetics
Research News and Information
Definition of 'INDEL Mutation'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. Common names: INDEL Mutation; INDEL Mutations; Mutation, INDEL; Mutations, INDEL; Insertion-Deletion Mutation; Insertion Deletion Mutation; Insertion-Deletion Mutations; Mutation, Insertion-Deletion; Mutations, Insertion-Deletion |
Saturday, March 20, 2010
29 Sep 2009 
OBJECTIVES: To determine the effects of the polymorphisms CFH Tyr402His and ARMS2 del443ins54 on susceptibility to age-related macular degeneration (AMD) and to find the frequencies of these single-nucleotide polymorphisms in an Italian population ... Read more...
Targeted capture and massively parallel sequencing of 12 human exomes.
14 Aug 2009 Genome-wide association studies suggest that common genetic variants explain only a modest fraction of heritable risk for common diseases, raising the question of whether rare variants account for a significant fraction of unexplained heritability. ... Read more...
A highly annotated whole-genome sequence of a Korean individual.
6 Jul 2009 Recent advances in sequencing technologies have initiated an era of personal genome sequences. To date, human genome sequences have been reported for individuals with ancestry in three distinct geographical regions: a Yoruba African, two individuals ... Read more...
Latest indexed articles for 'INDEL Mutation - Genetics'
These are the very latest articles for this heading:
- Typing of ARMS2 and CFH in age-related macular degeneration: case-control study and assessment of frequency in the Italian population. 29 Sep 2009
- Targeted capture and massively parallel sequencing of 12 human exomes. 14 Aug 2009
- A highly annotated whole-genome sequence of a Korean individual. 6 Jul 2009
- Ride the wavelet: A multiscale analysis of genomic contexts flanking small insertions and deletions. 3 Jun 2009
- Insertion/deletion polymorphism of angiotensin converting enzyme gene in Korean hypertensive adolescents. 22 May 2009
- Aromatase gene (CYP19A1) variants, female infertility and ovarian stimulation outcome: a preliminary report. 29 Apr 2009
- MMP-13 promoter polymorphisms in patients with chronic periodontitis: effects on GCF MMP-13 levels and outcome of periodontal therapy. 20 Apr 2009
- ACE insertion/deletion polymorphism and its relationships to the components of metabolic syndrome in elderly Slovaks. 27 Feb 2009
- Population genomics of domestic and wild yeasts. 9 Feb 2009
- Phylogenomics and protein signatures elucidating the evolutionary relationships among the Gammaproteobacteria. 30 Jan 2009
- Babesia microti-group parasites compared phylogenetically by complete sequencing of the CCTeta gene in 36 isolates.
30 Dec 2008 - Basing population genetic inferences and models of molecular evolution upon desired stationary distributions of DNA or protein sequences. 25 Dec 2008
- Evidence for a new root of the tree of life. 29 Nov 2008
- Identification of new variants within the two functional genes CCL3 and CCL3L encoding the CCL3 (MIP-1alpha) chemokine: implications for HIV-1 infection. 23 Nov 2008
- Insertion/deletion polymorphism of the angiotensin-converting enzyme gene is associated with schizophrenia in a Spanish population. 2 Nov 2008
- Using gene expression databases for classical trait QTL candidate gene discovery in the BXD recombinant inbred genetic reference population: mouse forebrain weight. 23 Sep 2008
- The pattern of insertion/deletion polymorphism in Arabidopsis thaliana. 7 Aug 2008
- Relationships between blood pressure, polymorphism of angiotensin-converting enzyme (ACE), body composition and biochemical characteristics in elderly Slovaks. 30 May 2008
- Mutation of a gene for thyroid transcription factor-1 (TITF1) in a patient with clinical features of resistance to thyrotropin. 26 May 2008
- Angiotensin-converting enzyme insertion/deletion gene polymorphic variant as a marker of coronary artery disease: a meta-analysis. 24 May 2008
See a longer list of these articles.
Technical information about 'INDEL Mutation'
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.
Descriptor UI: D054643
Alternative terms: INDEL Mutation; INDEL Mutations; Mutation, INDEL; Mutations, INDEL; Insertion-Deletion Mutation; Insertion Deletion Mutation; Insertion-Deletion Mutations; Mutation, Insertion-Deletion; Mutations, Insertion-Deletion;
Allowable Qualifiers: drug effects; genetics; immunology; physiology; radiation effects;
Tree Number: G05.355.600.370; G05.365.590.500;
History Note: 2008