Primary Identifier | MGI:5585501 | Allele Type | Spontaneous |
Gene | moct | Inheritance Mode | Recessive |
Strain of Origin | DDY | Is Recombinase | false |
Is Wild Type | false |
description | This heritable mutant phenotype was mapped to the 3.91 cM region encompassed by D2Mit467 and D2Mit320 on mouse chromosome 2 by linkage analysis (J:213627). Phenotypic Similarity to Human Syndrome: Cataract J:213627. |
molecularNote | This spontaneous mutation arose in the ddY strain (outbred colony) reared at Osaka Prefecture University. |