MS4A7 Back

membrane-spanning 4-domains, subfamily A, member 7

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NCBI Description of MS4A7
This gene encodes a member of the membrane-spanning 4A gene family, members of which are characterized by common structural features and similar intron/exon splice boundaries and display unique expression patterns in hematopoietic cells and nonlymphoid tissues. This family member is associated with mature cellular function in the monocytic lineage, and it may be a component of a receptor complex involved in signal transduction. This gene is localized to 11q12, in a cluster of other family members. At least four alternatively spliced transcript variants encoding two distinct isoforms have been observed.

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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).


Legend

MS4A7 is highly significantly mutated in
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MS4A7 is significantly mutated in
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MS4A7 is near significance in
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Click on a tumor type to see its full list of significant genes.

Data details


• Mutation list for MS4A7