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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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
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Gene expression in normal tissue: TIMM8A

Gene-model tissue-cancer distribution: Bubble Plot

undefinetissue: undefine cancer: undefined model num: 0undefinedtissue: undefined cancer: PANCAN model num: 1

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.
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
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Clinical Response
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