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Allele : Rtel1<tm2.1Hdin> regulator of telomere elongation helicase 1; targeted mutation 2.1, Hao Ding

Primary Identifier  MGI:5559530 Allele Type  Targeted
Gene  Rtel1 Transmission  Germline
Strain of Origin  (129X1/SvJ x 129S1/Sv)F1-Kitl<+> Is Recombinase  false
Is Wild Type  false
molecularNote  Exon 34 was replaced with a modified one in which nucleotide substitutions (ATC to GCC) result in the amino acid substitution of alanine for isoleucine at position 1169 (I1169A) and a V5 epitope tag. This mutation abolishes the PCNA-binding site. Cre-mediated recombination removed a floxed splice acceptor, IRES and beta-geo cassette inserted upstream of the modified exon 34.
  • mutations:
  • Insertion,
  • Nucleotide substitutions
  • synonyms:
  • RTEL1<IA>v5,
  • RTEL1<IA>v5
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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

4 Publication categories