NEU4

neuraminidase 4

Summary

The protein encoded by this gene belongs to a family of glycohydrolytic enzymes, which remove terminal sialic acid residues from various sialo derivatives, such as glycoproteins, glycolipids, oligosaccharides, and gangliosides. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Nov 2009]

Known Variants57 total

rsidPosition (GRCh37)AllelesClassClinVar
rs621930872:242,749,988A/Ccoding sequence variant—
rs3686125202:242,755,695G/A—likely benign
rs3749186502:242,755,748C/T—uncertain significance
rs7715316632:242,755,751G/A—uncertain significance
rs7771068882:242,755,758C/T—uncertain significance
rs17002440362:242,755,784A/C—uncertain significance
rs3681326722:242,755,806A/G—uncertain significance
rs7582945702:242,756,104G/A—uncertain significance
rs1491241082:242,756,152C/T—uncertain significance
rs7729265722:242,756,237C/T—uncertain significance
rs7562433252:242,756,255G/A—uncertain significance
rs12993571042:242,756,263T/C—uncertain significance
rs3737470972:242,756,284G/A—uncertain significance
rs7564003572:242,756,302G/T—uncertain significance
rs7802522962:242,756,305C/T—uncertain significance
rs7494318812:242,756,306G/A—uncertain significance
rs1167026462:242,756,317G/A—likely benign
rs5331656622:242,756,337C/T—likely benign
rs1383270252:242,757,391G/A—uncertain significance
rs3694473822:242,757,430C/T—uncertain significance
rs24697125042:242,757,433C/G—uncertain significance
rs7714979562:242,757,445G/A—uncertain significance
rs7503873362:242,757,470G/A—uncertain significance
rs1412979862:242,757,494G/A—uncertain significance
rs9615752172:242,757,499A/G—uncertain significance
rs3700022612:242,757,547C/T—uncertain significance
rs17003319462:242,757,556G/A—uncertain significance
rs3711408902:242,757,575G/A—uncertain significance
rs7637318642:242,757,619G/A—uncertain significance
rs5298252202:242,757,626T/C—uncertain significance
rs24697138502:242,757,692C/G—uncertain significance
rs8951070492:242,757,713G/A—uncertain significance
rs7459183032:242,757,759C/T—likely benign
rs3718520612:242,757,778G/A—uncertain significance
rs2007448092:242,757,794G/A—uncertain significance
rs7730171882:242,757,881C/T—uncertain significance
rs7620977092:242,757,910G/A—uncertain significance
rs14852138442:242,757,922A/G—uncertain significance
rs7786983582:242,757,965C/T—uncertain significance
rs7735405992:242,758,065C/G—uncertain significance
rs7540044672:242,758,076G/A—uncertain significance
rs7570374012:242,758,118C/T—uncertain significance
rs2013436212:242,758,127C/T—uncertain significance
rs7528027812:242,758,155C/G—uncertain significance
rs7488222202:242,758,180G/A—uncertain significance
rs3700210422:242,758,195G/A—uncertain significance
rs3735405922:242,758,198C/T—uncertain significance
rs7700275292:242,758,199C/T—uncertain significance
rs5630965882:242,758,202C/T—uncertain significance
rs1458978932:242,758,210G/T—uncertain significance
rs7699674202:242,758,237G/C—uncertain significance
rs5682893752:242,758,276T/C—uncertain significance
rs7521757212:242,758,291C/T—uncertain significance
rs5656703032:242,758,328C/T—uncertain significance
rs7646068382:242,758,352G/A—uncertain significance
rs7731199772:242,758,364G/T—uncertain significance
rs783534722:242,758,711C/T3 prime UTR variant—

Gene information from NCBI Gene. Variant classifications from ClinVar.