SLC6A14 Back

solute carrier family 6 (amino acid transporter), member 14

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NCBI Description of SLC6A14
This gene encodes a member of the solute carrier family 6. Members of this family are sodium and chloride dependent neurotransmitter transporters. The encoded protein transports both neutral and cationic amino acids. This protein may also function as a beta-alanine carrier. Mutations in this gene may be associated with X-linked obesity. A pseudogene of this gene is found on chromosome X. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments.

Community Annotation of SLC6A14 Add / Edit SLC6A14: Annotations

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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

SLC6A14 is highly significantly mutated in
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SLC6A14 is significantly mutated in
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SLC6A14 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 SLC6A14