ZBTB16

zinc finger and BTB domain containing 16

Summary

This gene is a member of the Krueppel C2H2-type zinc-finger protein family and encodes a zinc finger transcription factor that contains nine Kruppel-type zinc finger domains at the carboxyl terminus. This protein is located in the nucleus, is involved in cell cycle progression, and interacts with a histone deacetylase. Specific instances of aberrant gene rearrangement at this locus have been associated with acute promyelocytic leukemia (APL). Alternate transcriptional splice variants have been characterized. [provided by RefSeq, Jul 2008]

Known Variants65 total

rsidPosition (GRCh37)AllelesClassClinVar
rs74959797611:113,934,053C/T—likely benign
rs15070806611:113,934,112C/T—likely benign
rs20137267111:113,934,229C/T—likely benign
rs77228095511:113,934,283A/G—likely benign
rs3561676211:113,934,421G/A—benign
rs74560371811:113,934,424G/A—likely benign
rs14795134211:113,934,436C/T—likely benign
rs14962006811:113,934,448C/T—likely benign
rs36872588811:113,934,464C/T—uncertain significance
rs76336068111:113,934,465G/A—uncertain significance
rs20081130911:113,934,479C/G—uncertain significance
rs128047732511:113,934,551C/T—uncertain significance
rs11174654611:113,934,587A/G—likely benign
rs78122269211:113,934,612G/A—uncertain significance
rs3578483111:113,934,694C/G—likely benign
rs135368865211:113,934,700G/C—uncertain significance
rs57052829911:113,934,722C/T—uncertain significance
rs75632192411:113,934,726A/G—uncertain significance
rs74932093411:113,934,750C/T—uncertain significance
rs133868171911:113,934,778C/T—likely benign
rs77715528311:113,934,779A/G—likely benign
rs135225261411:113,934,794G/A—uncertain significance
rs14915316411:113,934,802C/T—likely benign
rs20022538711:113,934,835G/A—likely benign
rs19967660411:113,934,945C/A—uncertain significance
rs14329585711:113,934,961C/T—likely benign
rs129126173311:113,934,999C/T—uncertain significance
rs11375701811:113,935,027C/T—benign
rs14043344811:113,935,028G/A—uncertain significance
rs14565578411:113,935,051C/T—likely benign
rs37379835711:113,935,052G/A—uncertain significance
rs20070528811:113,935,069G/A—likely benign
rs14270909011:113,935,094G/A—likely benign
rs135503261211:113,935,106C/A—uncertain significance
rs13859484911:113,935,198T/C—likely benign
rs14926211211:113,935,205A/G—uncertain significance
rs53309651611:113,935,226A/G—uncertain significance
rs193903838811:113,935,244G/A—uncertain significance
rs147058252011:113,935,251G/A—uncertain significance
rs11606608211:113,935,270C/T—benign
rs178469211:113,949,232T/Cregulatory region variant—
rs260672511:113,955,303C/T——
rs1711633411:113,961,762C/Tupstream gene variant—
rs23891411:113,984,109C/Aintron variant—
rs321410111:114,009,408A/C——
rs37119745811:114,023,831A/G—likely benign
rs52749318411:114,025,967G/A——
rs37557336211:114,027,083G/A—likely benign
rs144116861711:114,027,093G/A—uncertain significance
rs11654729311:114,057,705C/T—likely benign
rs53984800111:114,061,890C/G——
rs57319511:114,088,038T/Gintron variant—
rs793673811:114,105,834A/T——
rs7790989011:114,110,367C/Aintron variant—
rs74770392811:114,112,898T/C—uncertain significance
rs254816583611:114,112,916T/C—uncertain significance
rs254816584711:114,112,928G/A—uncertain significance
rs14770979811:114,112,977C/T—likely benign
rs76098658911:114,113,066C/G—likely benign
rs11140090611:114,117,921C/T—likely benign
rs11595743511:114,117,994A/C—uncertain significance
rs12143460611:114,121,104A/Gmissense variantuncertain significance
rs76786034111:114,121,138C/T—uncertain significance
rs122198767411:114,121,253G/A—likely benign
rs74589431311:114,121,259C/T—likely benign

Gene information from NCBI Gene. Variant classifications from ClinVar.