Mitochondrial intermembrane space protein; forms a complex with Tim13p that delivers a subset of hydrophobic proteins to the TIM22 complex for inner membrane insertion; homolog of human TIMM8A, implicated in Mohr-Tranebjaerg syndrome, also known as deafness-dystonia-optic neuronopathy (DDON) syndrome; human TIMM8A can complement yeast null mutant [Source:SGD;Acc:S000007348]

Chromosome X: 676,971-677,234 forward strand.

This transcript has 1 exon, is annotated with 5 domains and features, is associated with 17 variant alleles and maps to 29 oligo probes.

This transcript is a product of gene YJR135W-A Show transcript tableHide transcript table