KCTD13

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An Error has occurred retrieving Wikidata item for infobox BTB/POZ domain-containing protein KCTD13 is a protein that in humans is encoded by the KCTD13 gene.[1][2]

Interactions

KCTD13 has been shown to interact with PCNA.[1]

Clinical relevance

Mutations in this gene have been associated to abnormalities in brain growth and behaviour.[3]

References

  1. 1.0 1.1 He H, Tan CK, Downey KM, So AG (October 2001). "A tumor necrosis factor alpha- and interleukin 6-inducible protein that interacts with the small subunit of DNA polymerase delta and proliferating cell nuclear antigen". Proceedings of the National Academy of Sciences of the United States of America. 98 (21): 11979–84. Bibcode:2001PNAS...9811979H. doi:10.1073/pnas.221452098. PMC 59753. PMID 11593007.
  2. "Entrez Gene: KCTD13 potassium channel tetramerisation domain containing 13".
  3. Arbogast T, Razaz P, Ellegood J, McKinstry SU, Erdin S, Currall B, et al. (May 2019). "Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactions". Human Molecular Genetics. 28 (9): 1474–1486. doi:10.1093/hmg/ddy436. PMC 6489413. PMID 30590535.

Further reading

External links

  • PDBe-KB provides an overview of all the structure information available in the PDB for Human KCTD13