amorphic allele - molecular evidence
Two separate single nucleotide deletions within POLDIP2 that results in a premature stop codon in both POLDIP2 isoforms.
Net deletion of two bases in the coding region of POLDIP2.
TC
female fertile (with POLDIP2KO1)
female fertile | dominant
male fertile | dominant
male semi-sterile (with POLDIP2KO1)
mitochondrial chromosome | spermatogenesis
spermatozoon