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SLC44A4

Official Full Name
solute carrier family 44 member 4
Organism
Homo sapiens
GeneID
80736
Background
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]
Synonyms
CTL4; NG22; TPPT; DFNA72; hTPPT1; C6orf29;

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