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

Gene information from NCBI Gene. Variant classifications from ClinVar.