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Allele : Tnnt1<tm1.2Jin> troponin T1, skeletal, slow; targeted mutation 1.2, Jian-Ping Jin

Primary Identifier  MGI:5635256 Allele Type  Targeted
Attribute String  Null/knockout Gene  Tnnt1
Transmission  Germline Strain of Origin  129P2/OlaHsd-Hprt1<b-m3>
Is Recombinase  false Is Wild Type  false
molecularNote  LoxP sites were inserted into intron 10 and intron 13. Cre-mediated recombination removed exons 11 through 13. The predicted truncated product mimicks the protein involved in Amish nemaline myopathy. A FRT-flanked neomycin resistance cassette was inserted into intron 10. Western blot analysis confirmed the absence of protein expression in the soleus muscle.
  • mutations:
  • Intragenic deletion,
  • Insertion
  • synonyms:
  • ssTnT-KO,
  • Tnnt1-exon 11-13 deletion,
  • Tnnt1-exon 11-13 deletion,
  • ssTnT-KO
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

6 Publication categories