======= KAT6A ======= == Gene Information == * **Official Symbol**: KAT6A * **Official Name**: lysine acetyltransferase 6A * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=7994|7994]] * **UniProt**: [[https://www.uniprot.org/uniprot/Q92794|Q92794]] * **Interactions**: [[https://thebiogrid.org/search.php?search=KAT6A&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20KAT6A|Open PubMed]] * **OMIM**: [[https://omim.org/entry/601408|Open OMIM]] == Function Summary == * **Entrez Summary**: This gene encodes a member of the MOZ, YBFR2, SAS2, TIP60 family of histone acetyltransferases. The protein is composed of a nuclear localization domain, a double C2H2 zinc finger domain that binds to acetylated histone tails, a histone acetyl-transferase domain, a glutamate/aspartate-rich region, and a serine- and methionine-rich transactivation domain. It is part of a complex that acetylates lysine-9 residues in histone 3, and in addition, it acts as a co-activator for several transcription factors. Allelic variants of this gene are associated with an autosomal dominant form of cognitive disability. Chromosomal translocations of this gene are associated with acute myeloid leukemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2017]. * **UniProt Summary**: Histone acetyltransferase that acetylates lysine residues in histone H3 and histone H4 (in vitro). Component of the MOZ/MORF complex which has a histone H3 acetyltransferase activity. May act as a transcriptional coactivator for RUNX1 and RUNX2. Acetylates p53/TP53 at 'Lys-120' and 'Lys-382' and controls its transcriptional activity via association with PML. {ECO:0000269|PubMed:11742995, ECO:0000269|PubMed:11965546, ECO:0000269|PubMed:12771199, ECO:0000269|PubMed:16387653, ECO:0000269|PubMed:17925393, ECO:0000269|PubMed:23431171}. |MOZ SAS| |PHD| |MOZ/MORF histone acetyltransferase complex| |H4 histone acetyltransferase activity| |acetyltransferase activity| |histone acetyltransferase complex| |cellular senescence| |histone H3 acetylation| |histone acetyltransferase activity| |histone H4 acetylation| |cell aging| |nucleosome| |PML body| |histone acetylation| |nucleosome assembly| |internal peptidyl-lysine acetylation| |peptidyl-lysine acetylation| |internal protein amino acid acetylation| |histone binding| |chromatin assembly| |protein acetylation| |chromatin assembly or disassembly| |nucleosome organization| |DNA packaging| |regulation of signal transduction by p53 class mediator| |protein acylation| |protein-DNA complex assembly| |myeloid cell differentiation| |nuclear chromatin| |protein-DNA complex subunit organization| |aging| |transcription coactivator activity| |DNA conformation change| |peptidyl-lysine modification| |transcription factor binding| |histone modification| |covalent chromatin modification| |nuclear speck| |hemopoiesis| |hematopoietic or lymphoid organ development| |immune system development| |chromatin organization| |zinc ion binding| |cellular protein-containing complex assembly| |nucleolus| |peptidyl-amino acid modification| |chromosome organization| |negative regulation of transcription, DNA-templated| |positive regulation of transcription by RNA polymerase II| |negative regulation of nucleic acid-templated transcription| |negative regulation of RNA biosynthetic process| |negative regulation of RNA metabolic process| |negative regulation of cellular macromolecule biosynthetic process| |negative regulation of nucleobase-containing compound metabolic process| |DNA binding| |negative regulation of macromolecule biosynthetic process| |negative regulation of cellular biosynthetic process| |positive regulation of transcription, DNA-templated| |negative regulation of biosynthetic process| |protein-containing complex assembly| |positive regulation of nucleic acid-templated transcription| |positive regulation of RNA biosynthetic process| |cellular response to stress| |negative regulation of gene expression| |positive regulation of RNA metabolic process| |regulation of intracellular signal transduction| |protein-containing complex subunit organization| |positive regulation of nucleobase-containing compound metabolic process| |positive regulation of macromolecule biosynthetic process| |positive regulation of cellular biosynthetic process| |positive regulation of gene expression| |positive regulation of biosynthetic process| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp21|MLN-4924 0.2μM R00 exp21]]|1.7| |[[:results:exp155|UNC1999 2μM R03 exp155]]|1.73| |[[:results:exp326|CCT251545 20μM R07 exp326]]|1.74| |[[:results:exp60|Vinblastine 0.002μM R01 exp60]]|1.74| |[[:results:exp10|CCCP 0.1μM R00 exp10]]|1.81| |[[:results:exp501|Methotrexate 0.01μM R08 exp501]]|1.86| |[[:results:exp175|3-Bromopyruvate 7μM R04 exp175]]|1.88| |[[:results:exp495|IWR1 50μM R08 exp495]]|1.88| |[[:results:exp47|Lapatinib 5μM R01 exp47]]|1.96| |[[:results:exp517|Quercetin 20μM R08 exp517]]|2.19| ^Gene^Correlation^ |[[:human genes:b:brpf1|BRPF1]]|0.492| 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**: 1166 * **Expression level (log2 read counts)**: 7.37 {{:chemogenomics:nalm6 dist.png?nolink |}}