| Primary Identifier | MGI:6404456 | Allele Type | Transgenic |
| Attribute String | Humanized sequence, Inserted expressed sequence, Reporter | Gene | Tg(CAG-PCCA*A138T,-EGFP)#Miab |
| Strain of Origin | FVB/N | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | The human PCCA cDNA containing an A to T mutation at position 138 in exon 5 and enhanced green fluorescent protein are under the control of the ubiquitously active CAG promoter. This mutation has been identified in propionic acidemia patients with mild to moderate symptoms. The pound symbol (#) is used when line is not specified and/or lines are pooled. |
