| Primary Identifier | MGI:1856145 | Allele Type | Spontaneous |
| Gene | Hps5 | Inheritance Mode | Recessive |
| Strain of Origin | DBA/2J | Is Recombinase | false |
| Is Wild Type | false |
| description | Shown to be an allele of the maroon mutation and later both were shown to be alleles of ru2. |
| molecularNote | This allele was initially shown to be allelic to Hps5ru2 and Hps5ru2-mr by complementation testing. The insertion of CCGG in codon 900 was identified by sequence analysis and putatively results in a frameshift mutation that precludes the translation of 118 carboxy terminal amino acids. |
