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Ask your administrator if you think this is wrong. ======= KLHL15 ======= == Gene Information == * **<color #00a2e8>Official Symbol</color>**: KLHL15 * **<color #00a2e8>Official Name</color>**: kelch like family member 15 * **<color #00a2e8>Aliases and Previous Symbols</color>**: N/A * **<color #00a2e8>Entrez ID</color>**: [[https://www.ncbi.nlm.nih.gov/gene/?term=80311|80311]] * **<color #00a2e8>UniProt</color>**: [[https://www.uniprot.org/uniprot/Q96M94|Q96M94]] * **<color #00a2e8>Interactions</color>**: [[https://thebiogrid.org/search.php?search=KLHL15&organism=9606|BioGRID]] * **<color #00a2e8>PubMed articles</color>**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20KLHL15|Open PubMed]] * **<color #00a2e8>OMIM</color>**: [[https://omim.org/entry/300980|Open OMIM]] == Function Summary == * **<color #00a2e8>Entrez Summary</color>**: 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]. * **<color #00a2e8>UniProt Summary</color>**: 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). {ECO:0000269|PubMed:14528312, ECO:0000269|PubMed:23135275, ECO:0000269|PubMed:27561354}. <button type='primary' size='sm' modal='Pfam_Domains'>Pfam Domains</button> <button type='primary' size='sm' modal='GO_terms'>GO Terms</button> <modal id='Pfam_Domains' size='lg' title='Pfam Domains'> |Kelch 1| |BTB| |BACK| </modal> <modal id='GO_terms' size='lg' title='GO Terms'> |nuclear protein quality control by the ubiquitin-proteasome system| |negative regulation of double-strand break repair via homologous recombination| |cellular response to misfolded protein| |response to misfolded protein| |protein quality control for misfolded or incompletely synthesized proteins| |negative regulation of double-strand break repair| |negative regulation of DNA repair| |Cul3-RING ubiquitin ligase complex| |negative regulation of DNA recombination| |regulation of double-strand break repair via homologous recombination| |regulation of double-strand break repair| |negative regulation of response to DNA damage stimulus| |regulation of DNA recombination| |negative regulation of DNA metabolic process| |regulation of DNA repair| |cellular response to topologically incorrect protein| |response to topologically incorrect protein| |regulation of response to DNA damage stimulus| |proteasome-mediated ubiquitin-dependent protein catabolic process| |proteasomal protein catabolic process| |regulation of DNA metabolic process| |ubiquitin-dependent protein catabolic process| |modification-dependent protein catabolic process| |modification-dependent macromolecule catabolic process| |proteolysis involved in cellular protein catabolic process| |cellular protein catabolic process| |protein catabolic process| |protein ubiquitination| |regulation of cellular response to stress| |protein modification by small protein conjugation| |cellular macromolecule catabolic process| |protein modification by small protein conjugation or removal| |macromolecule catabolic process| |organonitrogen compound catabolic process| |proteolysis| |negative regulation of nucleobase-containing compound metabolic process| |regulation of response to stress| |negative regulation of response to stimulus| |cellular response to stress| |organic substance catabolic process| |cellular catabolic process| </modal> \\ === CRISPR Data === <button type='primary' size='small' modal='Compound_Hit'>Compound Hit</button> <button type='default' size='small' modal='Most_Correlated_Genes'>Most Correlated Genes in Chemogenomics</button> <button type='primary' size='small' modal='Essential_Avana'>Tissues where Essential in the Avana Dataset (DepMap 20Q1)</button> <modal id='Compound_Hit' size='lg' title='Compound Hit'> ^Screen^Score^ |[[:results:exp365|I-BRD9 4μM R07 exp365]]|-2.06| </modal> <modal id='Most_Correlated_Genes' size='lg' title='Most Correlated Genes in Chemogenomics'> No correlation found to any other genes in chemogenomics. </modal> <modal id='Essential_Avana' size='lg' title='Tissues where Essential in the Avana Dataset (DepMap 20Q1)'> Global Fraction of Cell Lines Where Essential: 0/694 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|0/26| |bone|0/26| |breast|0/30| |central nervous system|0/49| |cervix|0/4| |colorectal|0/17| |esophagus|0/11| |fibroblast|0/1| |gastric|0/14| |kidney|0/18| |liver|0/19| |lung|0/72| |lymphocyte|0/16| |ovary|0/25| |pancreas|0/22| |peripheral nervous system|0/15| |plasma cell|0/12| |prostate|0/1| |skin|0/20| |soft tissue|0/9| |thyroid|0/2| |upper aerodigestive|0/22| |urinary tract|0/28| |uterus|0/5| </modal> == Essentiality in NALM6 == * **<color #00a2e8>Essentiality Rank</color>**: 15854 * **<color #00a2e8>Expression level (log2 read counts)</color>**: 5.71 <button type='primary' size='small' modal='Dist_expr'>Expression Distribution</button> <modal id='Dist_expr' size='lg' title='KLHL15 Expression in NALM6 Cells: 5.71'> {{:chemogenomics:nalm6 dist.png?nolink |}} </modal> Last modified: 2026/01/07 22:36by 127.0.0.1