KAT6A

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An Error has occurred retrieving Wikidata item for infobox K(lysine) acetyltransferase 6A (KAT6A), is an enzyme that, in humans, is encoded by the KAT6A gene.[1][2] This gene is located on human chromosome 8, band 8p11.21. [3]

Protein function

The KAT6A protein[4] contains two nuclear localization domains, a C2HC3 zinc finger and an acetyltransferase domain. This structure suggests that KAT6A functions as a chromatin-bound acetyltransferase.[2] KAT6A is important for the proper development of hematopoietic stem cells.[5]

Arboleda-Tham syndrome

Arboleda-Tham syndrome (ARTHS),[6] also referred to as KAT6A Syndrome (Arboleda-Tham Syndrome), is a rare autosomal dominant developmental disorder, caused by various missense, nonsense, and frameshift mutations in the KAT6A gene. The main characteristics of this syndrome are developmental delay, impaired intellectual development, speech delay, microcephaly, cardiac anomalies, and gastrointestinal complications. [7]

References

  1. "Entrez Gene: MYST3 MYST histone acetyltransferase (monocytic leukemia) 3".
  2. 2.0 2.1 Borrow J, Stanton VP, Andresen JM, Becher R, Behm FG, Chaganti RS, Civin CI, Disteche C, Dubé I, Frischauf AM, Horsman D, Mitelman F, Volinia S, Watmore AE, Housman DE (September 1996). "The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB-binding protein". Nat. Genet. 14 (1): 33–41. doi:10.1038/ng0996-33. PMID 8782817. S2CID 205342752.
  3. - KAT6A NCBI
  4. omim.org/entry/601408
  5. Yang XJ, Ullah M (August 2007). "MOZ and MORF, two large MYSTic HATs in normal and cancer stem cells". Oncogene. 26 (37): 5408–19. doi:10.1038/sj.onc.1210609. PMID 17694082.
  6. "OMIM Entry - # 616268 - ARBOLEDA-THAM SYNDROME; ARTHS".
  7. Kennedy, J., Goudie, D., Blair, E. et al. KAT6A Syndrome: genotype–phenotype correlation in 76 patients with pathogenic KAT6A variants. Genet Med 21, 850–860 (2019). https://doi.org/10.1038/s41436-018-0259-2

Further reading