External Ids for FIGNL1 Gene
GeneCards Summary for FIGNL1 Gene
FIGNL1 (Fidgetin-Like 1) is a Protein Coding gene. Diseases associated with FIGNL1 include autism spectrum disorder. GO annotations related to this gene include magnesium ion binding and nucleoside-triphosphatase activity. An important paralog of this gene is FIGN.
UniProtKB/Swiss-Prot for FIGNL1 Gene
Involved in DNA double-strand break (DBS) repair via homologous recombination (HR). Recruited at DSB sites independently of BRCA2, RAD51 and RAD51 paralogs in a H2AX-dependent manner. May regulate osteoblast proliferation and differentiation.