NTF4

neurotrophin 4

Summary

This gene is a member of a family of neurotrophic factors, neurotrophins, that control survival and differentiation of mammalian neurons. The expression of this gene is ubiquitous and less influenced by environmental signals. While knock-outs of other neurotrophins including nerve growth factor, brain-derived neurotrophic factor, and neurotrophin 3 prove lethal during early postnatal development, NTF5-deficient mice only show minor cellular deficits and develop normally to adulthood. [provided by RefSeq, Jul 2008]

Known Variants21 total

rsidPosition (GRCh37)AllelesClassClinVar
rs1166997719:49,564,124A/Gcoding sequence variant—
rs11596961719:49,564,512T/C—benign
rs56247439419:49,564,629C/T—uncertain significance
rs20067550919:49,564,630G/A—uncertain significance
rs12191842819:49,564,638C/Tmissense variantno classifications from unflagged records
rs12191842719:49,564,639G/Amissense variantuncertain significance
rs79704493919:49,564,734T/Cmissense variantpathogenic
rs76128234819:49,564,741C/T—uncertain significance
rs204013817519:49,564,777C/T—uncertain significance
rs37434513419:49,564,802C/T—likely benign
rs14484222019:49,564,858G/A—uncertain significance
rs36948407519:49,564,876C/A—uncertain significance
rs75204154219:49,564,932C/T—uncertain significance
rs75551860319:49,564,933G/A—uncertain significance
rs6173231019:49,564,992G/Amissense variantuncertain significance
rs20078611619:49,565,052C/T—benign
rs124464686219:49,565,095C/T—uncertain significance
rs101727482019:49,565,098G/A—uncertain significance
rs14775983719:49,565,330G/A—likely benign
rs7711320019:49,565,418A/G—likely benign
rs18321538819:49,568,050C/Gcoding sequence variant—

Gene information from NCBI Gene. Variant classifications from ClinVar.