Primary Identifier | MGI:1935122 | Allele Type | Spontaneous |
Gene | Fbn2 | Inheritance Mode | Recessive |
Strain of Origin | C.B10-H2<b>/LeMcdJ | Is Recombinase | false |
Is Wild Type | false |
molecularNote | This mutation consists of a 21 nucleotide deletion in the Fbn2 gene that removes that last 7 nucleotides of exon 38 and 14 nucleotides of intron 38, including the splice donor sequence. The mutation results in the aberrant skipping of exon 38. |