Concept information
Preferred term
t-Complex Genome Region
Type
-
mesh:Descriptor
Definition
- A 20 cM region of mouse chromosome 17 that is represented by a least two HAPLOTYPES. One of the haplotypes is referred to as the t-haplotype and contains an unusual array of mutations that affect embryonic development and male fertility. The t-haplotype is maintained in the gene pool by the presence of unusual features that prevent its recombination.
Broader concept
Entry terms
- t-Complex Region
Allowable Qualifier(s)
In other languages
-
French
URI
http://data.loterre.fr/ark:/67375/JVR-DX428DFR-T
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