Base Pair Mismatch [chybné párování bází]

topical
14
Terms

Base Pair Mismatches

Persistent link   https://www.medvik.cz/link/D020137
Definition

The presence of an uncomplimentary base in double-stranded DNA caused by spontaneous deamination of cytosine or adenine, mismatching during homologous recombination, or errors in DNA replication. Multiple, sequential base pair mismatches lead to formation of heteroduplex DNA; (NUCLEIC ACID HETERODUPLEXES).

DUI
D020137 MeSH Browser
CUI
M0029876
History note
1999
Public note
1999

Allowable subheadings

DE
drug effects 2
ES
ethics 0
GE
genetics 3
IM
immunology 0
PH
physiology 0
RE
radiation effects 0

G Phenomena and Processes
G05 Genetic Phenomena 135
G05.200 DNA Damage 956
G05.200.052 Base Pair Mismatch 14
G05.200.104 DNA Adducts 277
G05.200.210 DNA Breaks 13
G05.200.220 DNA Degradation, Necrotic 4
G05.200.230 DNA Fragmentation 90
G05.200.615 Pyrimidine Dimers 19
G05.365 Genetic Variation 858
G05.365.590 Mutation 4 993
G05.365.590.029 Allelic Imbalance 2
G05.365.590.060 Base Pair Mismatch 14
G05.365.590.175 Chromosome Aberrations 1 574
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 333
G05.365.590.320 Gene Duplication 65
G05.365.590.335 Genomic Instability 87
G05.365.590.350 Germ-Line Mutation 199
G05.365.590.500 INDEL Mutation 17
G05.365.590.538 Loss of Function Mutation 12
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 212
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
G05.365.590.917 Synthetic Lethal Mutations 4

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