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          <label>129S6/SvEvTac</label>
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                  <label>Inbred mouse strain</label>
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                  <label>FVB</label>
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                  <label>DBA</label>
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                  <label>SJL</label>
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                  <label>C3H</label>
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                <string>PMID: 10615122</string>
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                <string>Beck, J.A., et al., Genealogies of mouse inbred strains (2000), Nature, Jan2000, v24, p23</string>
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                <string>Inbr and colour depends on substrain (see below). Origin: Dunn 1928 from crosses of coat colour stocks from English fanciers and a chinchilla stock from Castle. This strain has a common origin with strain 101. Most substrains carry the white-bellied agouti gene AW though only a subset have the agouti pattern as many carry albino or chinchilla and/or the pink-eyed dilution gene, p, which is derived from Asian mice of the Mus musculus type (see also strains SJL, P/J and FS/Ei) (Brilliant et al, 1994).

It is known for the high incidence of spontaneous testicular teratomas, though the incidence differs between substrains, but more recently it has been the most widely used strain in the production of targeted mutations due to the availability of several lines of embryonic stem cells. Two recent studies show that there is major genetic variation within the 129 &quot;family&quot;, at least some of which must be attributed to genetic contamination (Threadgill et al, 1997,Simpson et al, 1997). Strain 129/SvJ was genetically contaminated in about 1978 by an unknown strain, and differs from other 129 substrains at about 25% of SSLP genetic markers. Threadgill et al suggest that it is equivalent to a recombinant congenic strain and suggest that it is designated 129cX/Sv. Simpson et al recognised three major groups of substrains: parental substrains, steel substrains and &quot;ter&quot; substrains. Threadgill et al identified substrains 129/Ola, 129/J, 129/Sv, 129/ReJ and 129/RrRk, and the associated embryonic stem cells.

Clearly, major revision of the nomenclature of this group of strains is necessary. This will be undertaken in the next revision. In the mean time, people doing targeted mutagenesis should take special care to ensure that the genotype of their embryonic stem cell culture matches the substrain of mice which they use.</string>
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                <string>2007-08-14</string>
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      <counter>0</counter>
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    <BioportalEntry>
      <strings>
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        <string>Beck, J.A., et al., Genealogies of mouse inbred strains (2000), Nature, Jan2000, v24, p23</string>
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        <string>Type: Inbred Strain
Type: Segregating Inbred
TJL Mating System: Sibling x Sibling         (Female x Male)
Species: laboratory mouse
H2 Haplotype: b
Generation: F155 (18-OCT-06)
Appearance
    pink-eyed, light-bellied chinchilla
    Related Genotype: Aw/Aw p Tyrc-ch/p Tyrc-ch

Important Note
    This strain is homozygous for Cdh23ahl, the age related hearing loss 1 mutation, which on this background results in progressive hearing loss with onset between 3 and 5 months of age.

Strain Description
    For a complete history of the numerous 129 substrains please refer to Simpson, et al., 1997. Historically, the 129 inbred mice are known for the high incidence of spontaneous testicular teratomas, though the incidence differs between substrains. Most recently 129 mice are widely used strain in the production of targeted mutations due to the availability of several lines of embryonic stem cells. There is major genetic variation within the 129 &quot;family&quot;, which has led to an update of the nomenclature and a division of substrains into three major groups: parental substrains, steel substrains and &quot;ter&quot; substrains. Investigators using 129 substrains for targeted mutagenesis should be careful in the selection of the appropriate 129 substrain to match the embryonic stem cell line.</string>
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        <string>obo_annot:modifiedDate</string>
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        <string>2007-08-23</string>
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    </BioportalEntry>
    <BioportalEntry>
      <strings>
        <string>birn_annot:jaxMiceID</string>
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      <list>
        <string>001137</string>
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    </BioportalEntry>
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</BioportalConcept>

