SLC44A4 - solute carrier family 44 member 4
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]
NCBI Orthologs
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Protein alignment
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Species | Gene | Architecture | aa |
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