Aliases for KLHL15 Gene
External Ids for KLHL15 Gene
Previous GeneCards Identifiers for KLHL15 Gene
This gene encodes a member of the kelch-like family of proteins that share a common domain structure consisting of an N-terminal broad-complex, tramtrack, bric-a-brac/poxvirus and zinc finger domain and C-terminal kelch repeat motifs. The encoded protein may be involved in protein ubiquitination and cytoskeletal organization. [provided by RefSeq, Apr 2009]
GeneCards Summary for KLHL15 Gene
KLHL15 (Kelch Like Family Member 15) is a Protein Coding gene. Diseases associated with KLHL15 include Mental Retardation, X-Linked 103 and Seckel Syndrome 2. An important paralog of this gene is KLHL9.
UniProtKB/Swiss-Prot Summary for KLHL15 Gene
Substrate-specific adapter for CUL3 E3 ubiquitin-protein ligase complex (PubMed:14528312). Acts as an adapter for CUL3 to target the serine/threonine-protein phosphatase 2A (PP2A) subunit PPP2R5B for ubiquitination and subsequent proteasomal degradation, thus promoting exchange with other regulatory subunits (PubMed:23135275). Acts as an adapter for CUL3 to target the DNA-end resection factor RBBP8/CtIP for ubiquitination and subsequent proteasomal degradation. Through the regulation of RBBP8/CtIP protein turnover, plays a key role in DNA damage response, favoring DNA double-strand repair through error-prone non-homologous end joining (NHEJ) over error-free, RBBP8-mediated homologous recombination (HR) (PubMed:27561354).