{"symbol":"SLC44A4","synonyms":["TPPT","CTL4","C6ORF29","DFNA72","hTPPT1","NG22"],"name":"solute carrier family 44, member 4","description":"The protein encoded by this gene may be a sodium-dependent transmembrane transport protein involved in the uptake of choline by cholinergic neurons. Defects in this gene can cause sialidosis, a lysosomal storage disease. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]","ncbiEntrezGeneId":80736,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/80736","proteins":[{"symbol":"CTL4_HUMAN","href":"/api/1.0/protein/CTL4_HUMAN"}],"hgncRootFamilies":[{"name":"Solute carriers (SLC)","href":"/api/1.0/gene_family/Solute+carriers+%28SLC%29"}]}