SLC44A4
solute carrier family 44 member 4 | CTL4, DFNA72, FLJ14491, NG22, TPPT, C6orf29

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]

Biological processes 31 terms
acetylcholine biosynthetic process (GO:0008292)acetylcholine secretion (GO:0061526)apical plasma membrane (GO:0016324)apical plasma membrane (GO:0016324)bile acid and bile salt transport (GO:0015721)choline transmembrane transporter activity (GO:0015220)choline transmembrane transporter activity (GO:0015220)choline transmembrane transporter activity (GO:0015220)choline transmembrane transporter activity (GO:0015220)choline transport (GO:0015871)choline transport (GO:0015871)choline transport (GO:0015871)extracellular exosome (GO:0070062)membrane (GO:0016020)neuromast hair cell development (GO:0035675)otolith formation (GO:0032475)phosphatidylcholine biosynthetic process (GO:0006656)phosphatidylcholine biosynthetic process (GO:0006656)plasma membrane (GO:0005886)plasma membrane (GO:0005886)plasma membrane (GO:0005886)positive regulation of cell growth (GO:0030307)thiamine pyrophosphate transmembrane transport (GO:0030974)thiamine pyrophosphate transmembrane transport (GO:0030974)thiamine pyrophosphate transmembrane transport (GO:0030974)thiamine pyrophosphate transmembrane transport (GO:0030974)thiamine pyrophosphate transmembrane transporter activity (GO:0090422)thiamine pyrophosphate transmembrane transporter activity (GO:0090422)thiamine pyrophosphate transmembrane transporter activity (GO:0090422)transmembrane transport (GO:0055085)transmembrane transporter activity (GO:0022857)
Expression (TPM)
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