HAMES_DBI.A6
Varsite
Name: sodium/glucose cotransporter 1
ID number: P13866
Uniprot ID: P13866
Tissue details: Lines the absorptive cells in the small intestine and proximal tubes in the kidney in order to uptake glucose in the cells.
Diseases: GGM (Congenital galactose/glucose malabsorption)
Tissue specificity: Expressed mainly in the intestine and kidney
Cofactors: cellular hexose transport, defective SLC5A1 causes congenital glucose/galactose malabsorption (GGM), intestinal hexose transport
Organs/systems of high level of expression: liver, heart, mouth
Organs/system of low level of expression: gonads, brain, pituitary gland
I. Three aspects that I am still curious about with my protein are the specifics of the disease that is caused by its mutation- GGM, it's role in other organisms besides humans, and more information on how it can be regulated by drugs and medication.
II. A potential research project would be looking into gene manipulation/editing and gene expression of SLC5A1 through CRISPR, and how it can correlate to GGM.
I love it!! Keep that reasearch idea in mind moving forward!
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