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SLCO1B7

solute carrier organic anion transporter family member 1B7 (putative)

HCNC Approved Symbol
SLCO1B7 (HGNC:32934)
Genomic Coordinates
12:19,800,001 - 21,100,000 (12p12.2)
Synonyms
LST3, SLC21A21
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
However, there are 3 patients* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.

SLCO1B7 - Gene browser | 3billion