GON4L

gon-4 like

Summary

Predicted to enable transcription corepressor activity. Predicted to be involved in negative regulation of DNA-templated transcription. Predicted to act upstream of or within B cell differentiation. Located in nuclear body. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants35 total

rsidPosition (GRCh37)AllelesClassClinVar
rs112644091:155,715,641G/Aregulatory region variant
rs7663473371:155,721,550G/Alikely benign
rs12194080001:155,721,939A/Glikely benign
rs17562361:155,721,974G/Tlikely benign
rs7453658011:155,722,089C/Tlikely benign
rs8921802881:155,722,092G/Alikely benign
rs5288966671:155,722,182C/Tlikely benign
rs7559437791:155,723,004G/Tuncertain significance
rs75504021:155,724,898T/G
rs5419617941:155,727,894G/A
rs1506852111:155,732,175C/Gbenign
rs13505090211:155,733,185T/Clikely benign
rs6078341:155,733,257T/Glikely benign
rs727061431:155,733,358G/Alikely benign
rs5594652991:155,735,148C/Tlikely benign
rs6772191:155,735,721A/Glikely benign
rs1500573881:155,735,790G/Abenign
rs1411218421:155,735,887T/Glikely benign
rs1447688371:155,735,988G/Clikely benign
rs1855845871:155,736,041C/Tlikely benign
rs617456011:155,736,258C/Tlikely benign
rs5345591071:155,738,015A/C
rs1438861961:155,741,005C/Tlikely benign
rs15532005631:155,742,897T/Cuncertain significance
rs1465045211:155,746,245G/Clikely benign
rs1432024911:155,747,464A/Glikely benign
rs29857071:155,749,870G/Aintron variant
rs2008015191:155,774,873A/Glikely benign
rs716286881:155,779,031G/A
rs1931148381:155,779,640A/Cintron variant
rs3686340281:155,783,530C/Tlikely benign
rs727061721:155,797,492A/G
rs1408936341:155,803,205C/Tintron variant
rs1472203721:155,823,496C/Tlikely benign
rs7757343661:155,823,498T/Clikely benign

Gene information from NCBI Gene. Variant classifications from ClinVar.