======= ERCC4 ======= == Gene Information == * **Official Symbol**: ERCC4 * **Official Name**: ERCC excision repair 4, endonuclease catalytic subunit * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=2072|2072]] * **UniProt**: [[https://www.uniprot.org/uniprot/Q92889|Q92889]] * **Interactions**: [[https://thebiogrid.org/search.php?search=ERCC4&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20ERCC4|Open PubMed]] * **OMIM**: [[https://omim.org/entry/133520|Open OMIM]] == Function Summary == * **Entrez Summary**: The protein encoded by this gene forms a complex with ERCC1 and is involved in the 5' incision made during nucleotide excision repair. This complex is a structure specific DNA repair endonuclease that interacts with EME1. Defects in this gene are a cause of xeroderma pigmentosum complementation group F (XP-F), or xeroderma pigmentosum VI (XP6).[provided by RefSeq, Mar 2009]. * **UniProt Summary**: Catalytic component of a structure-specific DNA repair endonuclease responsible for the 5-prime incision during DNA repair. Involved in homologous recombination that assists in removing interstrand cross-link. {ECO:0000269|PubMed:19596235}. |ERCC4| |regulation of double-stranded telomeric DNA binding| |negative regulation of double-stranded telomeric DNA binding| |nucleotide-excision repair involved in interstrand cross-link repair| |negative regulation of telomeric DNA binding| |regulation of protection from non-homologous end joining at telomere| |negative regulation of protection from non-homologous end joining at telomere| |telomeric DNA-containing double minutes formation| |3 overhang single-stranded DNA endodeoxyribonuclease activity| |nucleotide-excision repair factor 1 complex| |regulation of telomere maintenance in response to DNA damage| |negative regulation of telomere maintenance in response to DNA damage| |ERCC4-ERCC1 complex| |regulation of telomeric DNA binding| |telomerase inhibitor activity| |nucleotide-excision repair complex| |negative regulation of telomere capping| |endodeoxyribonuclease activity| |single-stranded DNA endodeoxyribonuclease activity| |TFIID-class transcription factor complex binding| |negative regulation of telomerase activity| |telomere maintenance via recombination| |UV protection| |mitotic recombination| |resolution of meiotic recombination intermediates| |nucleotide-excision repair, preincision complex stabilization| |nucleotide-excision repair, DNA incision, 3-to lesion| |meiotic chromosome separation| |global genome nucleotide-excision repair| |negative regulation of telomere maintenance via telomere lengthening| |regulation of telomere capping| |chromosome separation| |negative regulation of telomere maintenance| |nucleotide-excision repair, DNA incision, 5-to lesion| |transcription factor TFIID complex| |negative regulation of DNA biosynthetic process| |nucleotide-excision repair, DNA incision| |chromosome, telomeric region| |reciprocal meiotic recombination| |regulation of telomerase activity| |interstrand cross-link repair| |homologous recombination| |negative regulation of DNA binding| |damaged DNA binding| |double-strand break repair via nonhomologous end joining| |regulation of telomere maintenance via telomere lengthening| |non-recombinational repair| |transcription-coupled nucleotide-excision repair| |negative regulation of response to DNA damage stimulus| |regulation of telomere maintenance| |cellular response to UV| |meiotic chromosome segregation| |double-strand break repair via homologous recombination| |telomere maintenance| |recombinational repair| |telomere organization| |protein N-terminus binding| |single-stranded DNA binding| |nuclear chromosome, telomeric region| |meiosis I| |nucleotide-excision repair| |regulation of DNA biosynthetic process| |meiosis I cell cycle process| |cellular response to light stimulus| |negative regulation of DNA metabolic process| |regulation of DNA binding| |negative regulation of chromosome organization| |response to UV| |meiotic nuclear division| |meiotic cell cycle process| |negative regulation of binding| |cellular response to radiation| |double-strand break repair| |protein C-terminus binding| |regulation of response to DNA damage stimulus| |nuclear chromosome segregation| |DNA recombination| |meiotic cell cycle| |positive regulation of protein complex assembly| |chromosome segregation| |negative regulation of transferase activity| |nuclear division| |nucleic acid phosphodiester bond hydrolysis| |response to light stimulus| |organelle fission| |cellular response to environmental stimulus| |cellular response to abiotic stimulus| |regulation of autophagy| |anatomical structure homeostasis| |regulation of chromosome organization| |regulation of DNA metabolic process| |negative regulation of organelle organization| |regulation of binding| |response to radiation| |regulation of protein complex assembly| |DNA repair| |positive regulation of cellular component biogenesis| |negative regulation of cellular component organization| |regulation of cellular response to stress| |DNA metabolic process| |cellular response to DNA damage stimulus| |negative regulation of catalytic activity| |regulation of cellular catabolic process| |regulation of cellular component biogenesis| |regulation of transferase activity| |regulation of catabolic process| |cell cycle process| |chromosome organization| |identical protein binding| |negative regulation of molecular function| |response to abiotic stimulus| |positive regulation of cellular component organization| |regulation of organelle organization| |cell cycle| |negative regulation of cellular macromolecule biosynthetic process| |reproductive process| |reproduction| |negative regulation of nucleobase-containing compound metabolic process| |DNA binding| |negative regulation of macromolecule biosynthetic process| |regulation of response to stress| |negative regulation of cellular biosynthetic process| |negative regulation of biosynthetic process| |negative regulation of response to stimulus| |homeostatic process| |cellular response to stress| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp354|Diepoxybutane 3μM R07 exp354]]|-2.32| |[[:results:exp58|UM131593 0.1μM R01 exp58]]|-1.89| |[[:results:exp176|Apcin 50 to 100μM on day4 R04 exp176]]|-1.87| |[[:results:exp340|BN82002 4μM R07 exp340]]|-1.86| |[[:results:exp400|Senexin-A 25μM R07 exp400]]|-1.8| |[[:results:exp412|THZ531 0.11 to 0.125 to 0.35μM on day4 then day6 R07 exp412]]|-1.8| |[[:results:exp365|I-BRD9 4μM R07 exp365]]|-1.79| No correlation found to any other genes in chemogenomics. Global Fraction of Cell Lines Where Essential: 0/726 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|0/28| |bone|0/25| |breast|0/33| |central nervous system|0/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/15| |kidney|0/21| |liver|0/20| |lung|0/75| |lymphocyte|0/14| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|0/15| |prostate|0/1| |skin|0/24| |soft tissue|0/7| |thyroid|0/2| |upper aerodigestive|0/22| |urinary tract|0/29| |uterus|0/5| == Essentiality in NALM6 == * **Essentiality Rank**: 1543 * **Expression level (log2 read counts)**: 4.87 {{:chemogenomics:nalm6 dist.png?nolink |}}