QuickView for SLC44A4 (gene)

Gene Symbol:

SLC44A4 Homo sapiens

Full name:

solute carrier family 44 member 4

Synonyms:

C6orf29, CTL4, DFNA72, NG22, TPPT, hTPPT1, choline transporter-like protein 4, testicular tissue protein Li 48, thiamine pyrophosphate transporter, thiamine pyrophosphate transporter 1

Genomic Location:

Chr 6: 31938948-31954802

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.

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.

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Orthologs:

Mus musculus ,  Rattus norvegicus ,  D. melanogaster ,  Macaca mulatta ,  Danio rerio ,  Pan troglodytes ,  Canis lupus familiaris ,  Bos taurus

External Links:

Entrez Gene

Cytogenetic Map:

6p21.33

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