ADCY7

adenylate cyclase 7

Summary

This gene encodes a membrane-bound adenylate cyclase that catalyses the formation of cyclic AMP from ATP and is inhibitable by calcium. The product of this gene is a member of the adenylyl cyclase class-4/guanylyl cyclase enzyme family that is characterized by the presence of twelve membrane-spanning domains in its sequences. Several transcript variants have been observed for this gene, but the full-length natures of only two have been determined so far. [provided by RefSeq, Oct 2013]

Known Variants66 total

rsidPosition (GRCh37)AllelesClassClinVar
rs77237921516:50,279,994C/T——
rs2851480816:50,322,200C/T—uncertain significance
rs76902372716:50,322,218C/T—likely benign
rs37188923016:50,322,229G/A—uncertain significance
rs37714063916:50,324,369A/G—uncertain significance
rs76048971716:50,324,374T/C—conflicting classifications of pathogenicity
rs37693471816:50,324,449G/A—uncertain significance
rs37018813716:50,324,451C/T—likely benign
rs14002354816:50,324,468G/A—uncertain significance
rs77835635716:50,324,479G/T—uncertain significance
rs74718487816:50,325,705G/A—likely benign
rs250749544916:50,326,603T/C—uncertain significance
rs55005229816:50,326,670C/A—uncertain significance
rs124463177616:50,326,693G/A—uncertain significance
rs11415304616:50,332,805C/T—benign
rs98185715616:50,332,858A/G—uncertain significance
rs250766431516:50,332,862T/G—uncertain significance
rs7694295316:50,332,895C/T—benign
rs14764492716:50,332,900G/A—uncertain significance
rs250772847016:50,334,997G/A—uncertain significance
rs87912520616:50,335,059C/G—uncertain significance
rs7853476616:50,335,074C/Amissense variant—
rs95646765516:50,335,092G/A—uncertain significance
rs37082485816:50,338,323C/T—uncertain significance
rs75576350516:50,338,358C/T—uncertain significance
rs7449513716:50,338,367G/A—uncertain significance
rs144021064616:50,338,386G/T—uncertain significance
rs37374437516:50,338,439G/A—uncertain significance
rs77063290316:50,338,446A/G—uncertain significance
rs119325187316:50,338,846A/G—uncertain significance
rs77062324416:50,338,857C/T—uncertain significance
rs14760855316:50,338,858G/A—uncertain significance
rs203599925916:50,339,424C/T—uncertain significance
rs139252361816:50,339,476T/C—uncertain significance
rs1186133216:50,339,483G/A—benign
rs78070156616:50,339,487A/G—uncertain significance
rs77086319716:50,339,709T/A—uncertain significance
rs77518267116:50,340,988C/T—uncertain significance
rs14309835316:50,340,993C/T—likely benign
rs133384183016:50,340,994G/A—uncertain significance
rs14593341716:50,341,036G/A—likely benign
rs104759312916:50,341,044C/T—likely benign
rs14815577416:50,342,240C/T—likely benign
rs203621668016:50,342,242G/A—uncertain significance
rs75429854416:50,342,611A/G—uncertain significance
rs98188303116:50,342,636C/T—uncertain significance
rs20222091916:50,342,686G/C—uncertain significance
rs7944171416:50,342,712T/C—benign
rs76334767316:50,343,520C/T—likely benign
rs14084294516:50,343,540C/G—uncertain significance
rs20056796516:50,343,549C/A—uncertain significance
rs77078629416:50,344,617T/C—uncertain significance
rs77960387616:50,344,680T/C—uncertain significance
rs14641615516:50,345,641A/G—uncertain significance
rs37341740016:50,345,987A/T—uncertain significance
rs37603041316:50,346,034C/T—uncertain significance
rs250820135516:50,346,047A/G—uncertain significance
rs76761427316:50,346,099C/A—uncertain significance
rs94031065416:50,346,862A/G—uncertain significance
rs74588723416:50,346,942G/A—uncertain significance
rs14810339516:50,347,916C/T—likely benign
rs11660939916:50,347,949C/T—benign
rs77701380216:50,349,276G/A—uncertain significance
rs6173793816:50,349,326T/C—benign
rs53450493116:50,349,339G/A—uncertain significance
rs75472166916:50,349,406G/C—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.