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Allele : Ercc3<tm2Jhjh> excision repair cross-complementing rodent repair deficiency, complementation group 3; targeted mutation 2, Jan H J Hoeijmakers

Primary Identifier  MGI:3836429 Allele Type  Targeted
Gene  Ercc3 Transmission  Germline
Strain of Origin  129P2/OlaHsd Is Recombinase  false
Is Wild Type  false
molecularNote  The sequence at the intron exon boundary between intron 14 and exon 15 was modified from TCTCCCCACAG GCA TCC CGA CGC to TCTCCAG ACA GGC ATC TAG GCGC. These nucleotide substitutions alter the splice acceptor site and result in amino acid substitutions plus the formation of a stop codon that prevents the translation of the remaining 43 amino acids. 90% of transcripts utilize the alternative splice acceptor site while 10% utilize the endogenous splice acceptor site and produce full-length transcripts.
  • mutations:
  • Insertion,
  • Nucleotide substitutions
  • synonyms:
  • Xpb<delta43>,
  • Xpb<XPCS>,
  • Xpb<XPCS>,
  • Xpb<delta43>
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

0 Driven By

4 Publication categories