ADNP

activity dependent neuroprotector homeobox

Summary

Vasoactive intestinal peptide is a neuroprotective factor that has a stimulatory effect on the growth of some tumor cells and an inhibitory effect on others. This gene encodes a protein that is upregulated by vasoactive intestinal peptide and may be involved in its stimulatory effect on certain tumor cells. The encoded protein contains one homeobox and nine zinc finger domains, suggesting that it functions as a transcription factor. This gene is also upregulated in normal proliferative tissues. Finally, the encoded protein may increase the viability of certain cell types through modulation of p53 activity. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jul 2008]

Known Variants524 total

rsidPosition (GRCh37)AllelesClassClinVar
rs56538778120:49,506,366C/T—likely benign
rs99784912020:49,506,471G/A—likely benign
rs76124020:49,507,892T/G—benign
rs75040767220:49,507,947C/T—uncertain significance
rs212273307520:49,507,949T/C—uncertain significance
rs127499538920:49,507,951T/C—likely benign
rs212273311420:49,507,958C/T—uncertain significance
rs251557132720:49,507,959T/C—uncertain significance
rs78070668620:49,507,970C/A—uncertain significance
rs142223449020:49,507,971C/T—uncertain significance
rs14224708320:49,507,972G/A—likely benign
rs251557160420:49,507,985T/C—uncertain significance
rs77352027820:49,507,989T/C—uncertain significance
rs77454378220:49,507,993C/A—conflicting classifications of pathogenicity
rs198070433020:49,508,013T/C—uncertain significance
rs14739943220:49,508,015T/C—conflicting classifications of pathogenicity
rs251557198720:49,508,028C/T—likely benign
rs198070921120:49,508,029C/T—likely benign
rs76621485020:49,508,044A/T—likely benign
rs75114923720:49,508,045A/G—uncertain significance
rs135529104820:49,508,046T/C—uncertain significance
rs251557219520:49,508,059C/A—uncertain significance
rs74586125320:49,508,066A/G—likely benign
rs120610869620:49,508,073G/C—uncertain significance
rs75572793820:49,508,079A/G—conflicting classifications of pathogenicity
rs77815579920:49,508,084C/T—uncertain significance
rs74963630220:49,508,085G/A—conflicting classifications of pathogenicity
rs74632627420:49,508,095C/T—likely benign
rs37096823720:49,508,104A/G—likely benign
rs116527578920:49,508,107C/A—uncertain significance
rs251557275520:49,508,114T/C—uncertain significance
rs251557286820:49,508,129G/A—uncertain significance
rs145590279420:49,508,141T/G—uncertain significance
rs77319938620:49,508,147T/C—likely benign
rs14086732820:49,508,151C/T—likely benign
rs251557306920:49,508,152A/G—conflicting classifications of pathogenicity
rs76613352120:49,508,154A/G—uncertain significance
rs55991501520:49,508,156G/C—conflicting classifications of pathogenicity
rs139294694020:49,508,159C/T—conflicting classifications of pathogenicity
rs251557327420:49,508,172T/C—uncertain significance
rs137420849020:49,508,173C/A—uncertain significance
rs20051738920:49,508,175A/G—benign
rs198073868420:49,508,180T/A—uncertain significance
rs75581801220:49,508,181C/G—likely benign
rs117640109720:49,508,183C/T—uncertain significance
rs251557340320:49,508,185G/A—likely benign
rs15037476220:49,508,193G/C—likely benign
rs251557351320:49,508,194C/A—uncertain significance
rs124355075820:49,508,195A/G—uncertain significance
rs78033013620:49,508,199T/C—uncertain significance
rs93508971620:49,508,201G/C—benign
rs212273615320:49,508,211T/G—uncertain significance
rs133046808620:49,508,220G/A—uncertain significance
rs251557384920:49,508,231C/T—conflicting classifications of pathogenicity
rs77699944320:49,508,232T/C—uncertain significance
rs76203987220:49,508,234G/C—uncertain significance
rs75920807320:49,508,241C/G—likely benign
rs76731849620:49,508,242G/A—likely benign
rs74677413620:49,508,256C/T—uncertain significance
rs75326813820:49,508,257G/A—likely benign
rs101454681620:49,508,266G/A—likely benign
rs125158925620:49,508,273G/C—conflicting classifications of pathogenicity
rs56437325820:49,508,280T/C—likely benign
rs53123057320:49,508,283C/T—conflicting classifications of pathogenicity
rs18726619920:49,508,288G/A—uncertain significance
rs56810176020:49,508,291T/C—uncertain significance
rs14310306320:49,508,308C/A—likely benign
rs74582730120:49,508,309A/G—uncertain significance
rs77206826420:49,508,310C/G—uncertain significance
rs198076344920:49,508,313G/A—likely pathogenic
rs129558078420:49,508,318G/A—likely benign
rs14468499820:49,508,320T/C—likely benign
rs198076607420:49,508,328C/A—uncertain significance
rs14164308120:49,508,329A/T—likely benign
rs251557462520:49,508,332C/A—conflicting classifications of pathogenicity
rs251557465220:49,508,335A/G—benign
rs251557469820:49,508,340G/A—uncertain significance
rs251557473520:49,508,345G/C—uncertain significance
rs609616420:49,508,349C/T—uncertain significance
rs76118007720:49,508,350G/A—likely benign
rs76481728020:49,508,359C/T—benign
rs91324235120:49,508,366A/T—likely benign
rs251557498620:49,508,369T/A—uncertain significance
rs76704938220:49,508,374T/C—likely benign
rs137567445720:49,508,379C/A—uncertain significance
rs212273815220:49,508,393G/A—uncertain significance
rs36760512120:49,508,395T/G—likely benign
rs75608620920:49,508,400T/C—benign
rs128282469120:49,508,402T/C—conflicting classifications of pathogenicity
rs251557530820:49,508,408A/C—likely benign
rs55148524120:49,508,415T/C—conflicting classifications of pathogenicity
rs198078565820:49,508,430A/C—uncertain significance
rs77609003220:49,508,432T/G—uncertain significance
rs20110449820:49,508,436T/A—conflicting classifications of pathogenicity
rs37395127420:49,508,441T/A—uncertain significance
rs18469703520:49,508,442C/T—conflicting classifications of pathogenicity
rs58777752520:49,508,443——pathogenic
rs76695942220:49,508,443G/A—likely benign
rs251557567420:49,508,456T/C—likely benign
rs75213961220:49,508,463T/C—likely benign

Showing 100 of 524 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.