| Primary Identifier | MGI:5775395 | Allele Type | Targeted |
| Attribute String | Null/knockout, Reporter | Gene | Aplnr |
| Transmission | Germline | Strain of Origin | Not Specified |
| Is Recombinase | false | Is Wild Type | false |
| description | Phenotypic Similarity to Human Syndrome: Pulmonary Venoocclusive Disease J:227456. |
| molecularNote | Two loxP sites were inserted into the single exon flanking the coding region (base pairs 274-1407, total of 1134 bp) and nuclear lacZ following the second loxP site. The floxed exon was removed via cre-mediated recombination. |
