MTCH1 Back

mitochondrial carrier homolog 1 (C. elegans)

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NCBI Description of MTCH1

This gene encodes a member of the mitochondrial carrier family. The encoded protein is localized to the mitochondrion inner membrane and induces apoptosis independent of the proapoptotic proteins Bax and Bak. Pseudogenes on chromosomes 6 and 11 have been identified for this gene. Alternatively spliced transcript variants encoding multiple isoforms have been observed.

Community Annotation of MTCH1 Add / Edit MTCH1: Annotations

No community annotations yet for MTCH1.
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Figure notes

• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


MTCH1 is highly significantly mutated in
MTCH1 is significantly mutated in
MTCH1 is near significance in

Click on a tumor type to see its full list of significant genes.

Data details

Mutation list for MTCH1