| Primary Identifier | MGI:6393997 | Allele Type | Targeted |
| Attribute String | Humanized sequence | Gene | Hmbs |
| Transmission | Germline | Strain of Origin | 129/Sv x C57BL/6 |
| Is Recombinase | false | Is Wild Type | false |
| molecularNote | A G to A change at position 500 resulting in an arginine to glutamine substitution at amino acid 167 (R167Q) was introduced in exon 10 and a loxP-flanked neomycin cassette was inserted in intron 9. The neomycin selection cassette was removed via cre-mediated recombination. This is a mutation found in human dominant acute intermittent porphyria. |
