| Primary Identifier | MGI:1856819 | Allele Type | Spontaneous |
| Gene | Rab38 | Inheritance Mode | Recessive |
| Strain of Origin | C57BL/6J | Is Recombinase | false |
| Is Wild Type | false |
| description | This allele has been maintained on the C57BL/6J background at The Jackson Laboratory since 1984 when it was first identified. |
| molecularNote | A G-to-T transversion mutation at coding nucleotide 56 (c.56G>T) in exon 1 results in a glycine to valine substitution in codon 19 of the gene (p.G19V). This mutation lies within the highly conserved phosphate/Mg2+ domain. |
