JAG2

jagged canonical Notch ligand 2

Summary

The Notch signaling pathway is an intercellular signaling mechanism that is essential for proper embryonic development. Members of the Notch gene family encode transmembrane receptors that are critical for various cell fate decisions. The protein encoded by this gene is one of several ligands that activate Notch and related receptors. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

Known Variants190 total

rsidPosition (GRCh37)AllelesClassClinVar
rs37016769914:105,609,028G/A—likely benign
rs20155797814:105,609,043C/T—likely benign
rs19968206314:105,609,046C/T—likely benign
rs58770636214:105,609,060T/C—uncertain significance
rs37575128414:105,609,096C/A—uncertain significance
rs36823265214:105,609,110G/A—likely benign
rs312238214:105,609,113C/T—likely benign
rs20203968714:105,609,114G/A—likely benign
rs137840338214:105,609,129C/T—uncertain significance
rs37514490514:105,609,144G/A—uncertain significance
rs132491323814:105,609,158G/A—likely benign
rs254285625514:105,609,188C/G—uncertain significance
rs36784467314:105,609,208C/T—uncertain significance
rs254285634814:105,609,211C/T—uncertain significance
rs75000717114:105,609,212C/G—uncertain significance
rs14881536914:105,609,229C/T—uncertain significance
rs58764795114:105,609,235C/T—uncertain significance
rs76448022214:105,609,246G/A—uncertain significance
rs77869220414:105,609,267G/A—uncertain significance
rs18809211214:105,609,274G/A—uncertain significance
rs20043951814:105,609,278C/T—likely benign
rs37330205814:105,609,281C/T—likely benign
rs14343861714:105,609,282G/A—uncertain significance
rs37735029814:105,609,310C/T—uncertain significance
rs14603713914:105,609,325C/T—likely benign
rs13877938614:105,609,326C/T—likely benign
rs1014922914:105,609,335G/A—benign
rs3530411414:105,609,359C/T—benign
rs75271285614:105,609,360G/A—uncertain significance
rs13820410514:105,609,380G/A—benign
rs3472876614:105,609,400G/Amissense variantlikely benign
rs37561014314:105,609,420C/T—uncertain significance
rs77491420114:105,609,442C/A—uncertain significance
rs19970626714:105,609,458C/T—likely benign
rs7491364414:105,609,836G/A—benign
rs14636640214:105,609,841A/C—likely benign
rs133882721314:105,609,904G/A—likely benign
rs76758127814:105,609,907G/A—likely benign
rs11700710814:105,609,928G/A—benign
rs77738358314:105,609,947T/C—uncertain significance
rs133749488714:105,609,965G/A—uncertain significance
rs18946756214:105,611,295G/A—uncertain significance
rs76709233214:105,611,301G/A—likely benign
rs14017376414:105,611,305G/A—uncertain significance
rs188818063014:105,611,347T/C—uncertain significance
rs148693102214:105,611,364C/T—uncertain significance
rs76159526914:105,611,371C/T—uncertain significance
rs76634696814:105,611,383C/T—uncertain significance
rs37555024214:105,612,062C/T—likely benign
rs77058732714:105,612,076C/T—uncertain significance
rs36819174714:105,612,084C/T—uncertain significance
rs20217818214:105,612,085G/A—uncertain significance
rs214097145814:105,612,090A/G—uncertain significance
rs76275843914:105,612,094G/A—uncertain significance
rs13884385314:105,612,097A/G—likely benign
rs14888554014:105,612,131G/A—likely benign
rs74862092514:105,612,135C/T—uncertain significance
rs75886752314:105,612,136G/A—uncertain significance
rs14573738114:105,612,169C/T—benign
rs58766988814:105,612,170G/A—likely benign
rs188820684014:105,612,187C/T—uncertain significance
rs75311943514:105,612,239C/T—likely benign
rs37256739814:105,612,257G/A—likely benign
rs75187410214:105,612,277C/T—uncertain significance
rs15061686714:105,612,798G/A—uncertain significance
rs75417384214:105,612,804C/T—uncertain significance
rs76478411814:105,612,808G/A—uncertain significance
rs77149430114:105,612,939G/C—likely benign
rs13975128714:105,613,018C/T—benign
rs75727128914:105,613,019G/A—uncertain significance
rs78173478014:105,613,026C/T—likely pathogenic
rs11390643814:105,613,039C/T—benign
rs77275147214:105,613,056C/T—uncertain significance
rs145972626614:105,613,669G/A—uncertain significance
rs254286818214:105,613,673G/C—uncertain significance
rs14844003214:105,613,683G/A—uncertain significance
rs140272665314:105,613,708G/A—uncertain significance
rs75747809614:105,613,720C/T—likely benign
rs75551384214:105,613,754G/A—likely benign
rs14756809214:105,613,842C/A—likely benign
rs11294839514:105,614,103A/G—benign
rs77693612514:105,614,123C/T—uncertain significance
rs75971581014:105,614,124G/A—uncertain significance
rs14192586214:105,614,137G/A—benign
rs76450234714:105,614,141C/T—uncertain significance
rs99955631514:105,614,166C/T—uncertain significance
rs77966196514:105,614,221C/T—likely benign
rs37631613614:105,614,233G/T—likely benign
rs77893177414:105,614,456C/T—likely benign
rs74678975114:105,614,492C/T—uncertain significance
rs135103954314:105,614,503G/A—uncertain significance
rs76414607914:105,614,663G/A—conflicting classifications of pathogenicity
rs19288737714:105,614,696C/T—uncertain significance
rs7536277614:105,614,697G/A—benign
rs214097487814:105,614,704C/G—uncertain significance
rs7815427714:105,614,734C/T—conflicting classifications of pathogenicity
rs19966525514:105,614,740C/T—uncertain significance
rs20070828414:105,614,753G/A—uncertain significance
rs14497798514:105,614,769G/A—likely benign
rs224263414:105,615,026A/T——

Showing 100 of 190 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.