SLC13A5

Solute carrier family 13 (sodium-dependent citrate transporter), member 5
Identifiers
Symbols SLC13A5 ; EIEE25; NACT; mIndy
External IDs OMIM: 608305 HomoloGene: 21941 GeneCards: SLC13A5 Gene
Orthologs
Species Human Mouse
Entrez 284111 237831
Ensembl ENSG00000141485 ENSMUSG00000020805
UniProt Q86YT5 Q67BT3
RefSeq (mRNA) NM_001143838 NM_001004148
RefSeq (protein) NP_001137310 NP_001004148
Location (UCSC) Chr 17:
6.68 – 6.71 Mb
Chr 11:
72.24 – 72.27 Mb
PubMed search

Solute carrier family 13 (sodium-dependent citrate transporter), member 5 also known as the Na+/citrate cotransporter is a protein that in humans is encoded by the SLC13A5 gene.[1]

Function

SLC13A5 is a tricarboxylate plasma transporter with a preference for citrate.[1]

Clinical significance

In 2014, by means of exome sequencing it was determined that a genetic mutation of the SLC13A5 gene is the cause of an extremely rare citrate transporter disorder.[2]

Mutations in SLC13A5 cause autosomal recessive epileptic encephalopathy with seizure onset in the first days of life.[2] Those afflicted suffer from seizures, global developmental delay, movement disorder and hypotonia.

The site www.citratetransporterdisorders.org aims to unite families, doctors and researchers in their efforts to find treatment options.

References

Further reading

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


This article is issued from Wikipedia - version of the Sunday, January 31, 2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.