SLC5A3 (NP_008864, 533 a.a. ~ 641 a.a) partial recombinant protein with GST tag. The sequence is TPPPTKEQIRTTTFWSKKNLVVKENCSPKEEPYKMQEKSILRCSENNETINHIIPNGKSE DSIKGLQPEDVNLLVTCREEGNPVASLGHSEAETPVDAYSNGQAALMGE
Conjugate
Unconjugated
Target
Alternative Names
SLC5A3; solute carrier family 5 (sodium/myo-inositol cotransporter), member 3; BCW2; SMIT; SMIT1; SMIT2; sodium/myo-inositol cotransporter; Na(+)/myo-inositol cotransporter; sodium/myo-inositol transporter 1; sodium/myo-inositol cotransporter 1; solute ca
SLC5A3 (solute carrier family 5 (sodium/myo-inositol cotransporter), member 3) is a protein-coding gene. Diseases associated with SLC5A3 include down syndrome, and brain injury, and among its related super-pathways are Transmembrane transport of small molecules and Glucose transport. GO annotations related to this gene include myo-inositol:sodium symporter activity. An important paralog of this gene is SLC5A8.
Pathway
Disease; Hexose transport; Metabolism; Myoclonic epilepsy of Lafora
Citations
Publication ()
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