Description : 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]

Gene families : OG_03_0004564 (OF) Phylogenetic Tree(s): OG0004564_tree

Sequence : coding (download), protein (download)

Note:Only the main profile, including all conditions, is shown. Additional statistics and tissue specific profiles are available here.

Type Description Actions
Neighborhood HRR: YJR135W-A
Cluster HCCA: Cluster_67

Target Alias Description ECC score Gene Family Method Actions
CBF77867 No alias hypothetical protein 0.05 OF
EDN90624 No alias Tim10-like 0.02 OF
EDO65121 No alias Tim10-like 0.02 OF
EGR48845 No alias Tim10-like 0.07 OF
KHC79321 No alias mitochondrial import inner membrane translocase subunit... 0.04 OF
SPAC13G6.04.1 No alias TIM22 inner membrane protein import complex subunit Tim8... 0.04 OF

Type GO Term Name Evidence Source

No GO annotation available for this sequence

Type GO Term Name Evidence Source

No Predicted GO terms available for this sequence

InterPro domains Description Start Stop
IPR004217 Tim10-like 23 84
No external refs found!