IPP

intracisternal A particle-promoted polypeptide

Summary

The protein encoded by this gene is a member of the kelch family of proteins, which is characterized by a 50 amino acid repeat which interacts with actin. Transcript variants have been described but their full-length nature has not been determined. [provided by RefSeq, Jul 2008]

Known Variants33 total

rsidPosition (GRCh37)AllelesClassClinVar
rs1167922741:46,165,539C/Tupstream gene variant—
rs7545188551:46,165,652C/T—uncertain significance
rs11900208941:46,165,654C/T—uncertain significance
rs12742473441:46,165,666C/T—uncertain significance
rs16454308671:46,165,709G/A—uncertain significance
rs7652022431:46,165,717T/C—uncertain significance
rs14125658551:46,165,811C/A—uncertain significance
rs13351657191:46,165,837A/G—uncertain significance
rs715000871:46,174,921G/T——
rs617848011:46,179,022A/T——
rs5729922511:46,180,037T/C—uncertain significance
rs7692942671:46,182,596C/T—uncertain significance
rs1384453151:46,182,656A/G—uncertain significance
rs5448036411:46,184,878A/T—uncertain significance
rs7501782501:46,184,923G/A—uncertain significance
rs7622677001:46,184,940G/A—uncertain significance
rs7568987151:46,193,362T/C—uncertain significance
rs5364525361:46,193,465A/G—uncertain significance
rs5625748411:46,195,364C/G—uncertain significance
rs5423554931:46,195,378C/T—uncertain significance
rs3721246981:46,195,392C/A—uncertain significance
rs1833154071:46,201,427G/Aregulatory region variant—
rs2014045641:46,206,577T/C—uncertain significance
rs1502121831:46,206,614A/C—uncertain significance
rs3680287961:46,206,630G/C—uncertain significance
rs7789810731:46,206,647T/C—uncertain significance
rs25231345991:46,206,686G/A—uncertain significance
rs16460565671:46,206,689G/C—uncertain significance
rs11886396511:46,206,935T/C—uncertain significance
rs617848241:46,211,347A/Gintron variant—
rs7495511621:46,211,930G/A—uncertain significance
rs2011491671:46,211,953C/T—uncertain significance
rs7625624361:46,211,981G/A—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.