284111237831ENSG00000141485ENSMUSG00000020805Q86YT5Q67BT3NM_001143838NM_001284509NM_001284510NM_177550NM_001004148NM_001372402NM_001372403NP_001137310NP_001271438NP_001271439NP_808218NP_001004148NP_001359331NP_001359332Solute carrier family 13 (sodium-dependent citrate transporter), member 5 also known as the Na+/citrate cotransporter or mIndy is a protein that in humans is encoded by the SLC13A5 gene.

[5] In 2014, by means of exome sequencing it was determined that a genetic mutation of the SLC13A5 gene is the cause of a rare citrate transporter disorder.

[6] Those afflicted suffer from seizures, global developmental delay, movement disorder and hypotonia.

Reduced expression of this gene is associated with longer lifespan in many organisms, including some non-human primates.

[7] This article incorporates text from the United States National Library of Medicine, which is in the public domain.