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Allele : Itfg2<em1(IMPC)J> integrin alpha FG-GAP repeat containing 2; endonuclease-mediated mutation 1, Jackson

Primary Identifier  MGI:6111974 Allele Type  Endonuclease-mediated
Attribute String  Null/knockout Gene  Itfg2
Inheritance Mode  Not Specified Strain of Origin  C57BL/6NJ
Is Recombinase  false Is Wild Type  false
Project Collection  IMPC
molecularNote  This allele was generated at The Jackson Laboratory by injecting Cas9 RNA and 4 guide sequences GGGTTCCTGGGCAGACCCCA, AACACTGCACATGTGCACCA, GGTTTGTCCATATAGCAAAG and TCGAGATGAATGTTCTCTCT, which resulted in a 507 bp deletion beginning at Chromosome 6 negative strand position 128,416,346 bp and ending after 128,415,840 bp (GRCm38/mm10). This mutation deletes ENSMUSE00001296813 and ENSMUSE00001250898 (exons 3 and 4) and 296 bp of flanking intronic sequence including the splice acceptors and donors. In addition, there are 2 small intronic indels, a 1 bp (G) deletion 108 bp before the exon deletion and a 2 bp deletion (GT) 62 bp after the deletion that will not alter the results of the exons being deleted. This mutation is predicted to cause a change of amino acid sequence after residue 64 and early truncation 9 amino acids later.
  • mutations:
  • Intragenic deletion
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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