| Primary Identifier | MGI:5607160 | Allele Type | Chemically induced (ENU) |
| Attribute String | Not Specified | Gene | Scn8a |
| Inheritance Mode | Recessive | Strain of Origin | C57BL/6J |
| Is Recombinase | false | Is Wild Type | false |
| Project Collection | Beutler Mutagenetix |
| molecularNote | The molecular lesion is an A to G transition at base pair 101,035,646 (v38) on chromosome 15, or base pair 165,824 in the GenBank genomic region NC_000081. This corresponds to nucleotide 4,883 in the mRNA sequence NM_001077499 within exon 26 of 27 total exons. The mutation results in a tyrosine (Y) to cysteine (C) substitution at amino acid 1577 (Y1577C) in the SCN8A protein. |
