TIMM8A
Summary: This translocase is involved in the import and insertion of hydrophobic membrane proteins from the cytoplasm into the mitochondrial inner membrane. The gene is mutated in Mohr-Tranebjaerg syndrome/Deafness Dystonia Syndrome (MTS/DDS) and it is postulated that MTS/DDS is a mitochondrial disease caused by a defective mitochondrial protein import system. Defects in this gene also cause Jensen syndrome; an X-linked disease with opticoacoustic nerve atrophy and muscle weakness. This protein, along with TIMM13, forms a 70 kDa heterohexamer. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Mar 2009].
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Name | OMIM ID | Ensembl ID | HGNC ID | PHARMGKB ID | Map Location |
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OMIM IDMIM:300356 Ensembl IDEnsembl:ENSG00000126953 HGNC IDHGNC:HGNC:11817 PHARMGKB IDPA36523 Map LocationXq22.1 |
GO terms in TIMM8A
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Term Type | Evidence Type | GO Term ID | GO Des. |
---|---|---|---|
BP | TAS | GO:0007399 | nervous system development |
BP | TAS | GO:0072321 | chaperone-mediated protein transport |
CC | HDA | GO:0005739 | mitochondrion |
CC | IDA | GO:0005739 | mitochondrion |
CC | IEA | GO:0005743 | mitochondrial inner membrane |
CC | IDA | GO:0005758 | mitochondrial intermembrane space |
Gene expression in normal tissue: TIMM8A
Gene-model tissue-cancer distribution: Bubble Plot
Gene-drug pathway distribution
Pathways in TIMM8A
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Database | Pathway ID | Pathway Des. |
---|---|---|
reactome | R-HSA-1268020 | Mitochondrial protein import |
reactome | R-HSA-392499 | Metabolism of proteins |
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Gene-Drug: Aster Plot
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Drug ID | Drug Name | Model Num. |
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iGMDRD68 | Paclitaxel | 1 |
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Gene in drug-gene network: Network Plot

Gene-drug targets distribution
Gene Structure: PDB
Models in TIMM8A
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Model | Level | Reference ID | Tissue | Cancer | Drug | Clinical Response | Source | |
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No matching records found |