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KAT6A

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(Redirected from MYST3) Protein-coding gene in the species Homo sapiens
KAT6A
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

1M36, 2LN0, 2OZU, 2RC4, 3V43, 4LJN, 4LK9, 4LKA, 4LLB

Identifiers
AliasesKAT6A, MOZ, MYST3, RUNXBP2, ZC2HC6A, ZNF220, MRD32, MYST-3, lysine acetyltransferase 6A, ARTHS
External IDsOMIM: 601408; MGI: 2442415; HomoloGene: 4924; GeneCards: KAT6A; OMA:KAT6A - orthologs
Gene location (Human)
Chromosome 8 (human)
Chr.Chromosome 8 (human)
Chromosome 8 (human)Genomic location for KAT6AGenomic location for KAT6A
Band8p11.21Start41,929,479 bp
End42,051,994 bp
Gene location (Mouse)
Chromosome 8 (mouse)
Chr.Chromosome 8 (mouse)
Chromosome 8 (mouse)Genomic location for KAT6AGenomic location for KAT6A
Band8|8 A2Start23,349,551 bp
End23,433,275 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • nipple

  • internal globus pallidus

  • lactiferous duct

  • skin of arm

  • skin of thigh

  • mucosa of ileum

  • skin of hip

  • epithelium of colon

  • cardia

  • vulva
Top expressed in
  • Gonadal ridge

  • retinal pigment epithelium

  • molar

  • tibiofemoral joint

  • lacrimal gland

  • left lung lobe

  • cerebellar vermis

  • vas deferens

  • ciliary body

  • blood
More reference expression data
BioGPS


More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

7994

244349

Ensembl

ENSG00000083168

ENSMUSG00000031540

UniProt

Q92794

Q8BZ21

RefSeq (mRNA)

NM_001099412
NM_001099413
NM_001305878
NM_006766

NM_001081149
NM_001364449

RefSeq (protein)

NP_001292807
NP_006757

NP_001074618
NP_001351378

Location (UCSC)Chr 8: 41.93 – 42.05 MbChr 8: 23.35 – 23.43 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

K(lysine) acetyltransferase 6A (KAT6A), is an enzyme that, in humans, is encoded by the KAT6A gene. This gene is located on human chromosome 8, band 8p11.21.

Protein function

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

Arboleda-Tham syndrome

Main article: Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome

Arboleda-Tham syndrome (ARTHS), 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.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000083168Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000031540Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: MYST3 MYST histone acetyltransferase (monocytic leukemia) 3".
  6. ^ 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.
  7. - KAT6A NCBI
  8. omim.org/entry/601408
  9. 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.
  10. "OMIM Entry - # 616268 - ARBOLEDA-THAM SYNDROME; ARTHS".
  11. 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

PDB gallery
  • 1m36: Solution Structure of a CCHC Zinc Finger from MOZ 1m36: Solution Structure of a CCHC Zinc Finger from MOZ
  • 2ozu: Crystal structure of human MYST histone acetyltransferase 3 in complex with acetylcoenzyme A 2ozu: Crystal structure of human MYST histone acetyltransferase 3 in complex with acetylcoenzyme A


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