| Primary Identifier | MGI:5444299 | Allele Type | Spontaneous |
| Gene | Sh3tc2 | Strain of Origin | B6.129P2-Cnr2<tm1Dgen>/J |
| Is Recombinase | false | Is Wild Type | false |
| molecularNote | The mutation is identified as a C-to-T substitution at coding nucleotide 211 (c.211C>T) in exon 3 of 17 exons. The mutation alters the corresponding amino acid from glutamine to a stop codon at position 71 (p.Q71*). |
