KCTD12

BTB/POZ domain-containing protein KCTD12 is a protein that in humans is encoded by the KCTD12 gene.[5][6]

KCTD12
Identifiers
AliasesKCTD12, C13orf2, PFET1, PFETIN, potassium channel tetramerization domain containing 12
External IDsOMIM: 610521 MGI: 2145823 HomoloGene: 16316 GeneCards: KCTD12
Orthologs
SpeciesHumanMouse
Entrez

115207

239217

Ensembl

ENSG00000178695

ENSMUSG00000098557

UniProt

Q96CX2

Q6WVG3

RefSeq (mRNA)

NM_138444

NM_177715

RefSeq (protein)

NP_612453

NP_808383

Location (UCSC)Chr 13: 76.88 – 76.89 MbChr 14: 103.21 – 103.22 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

It may be associated with rumination[7] and Bipolar Disorder.[8]

References

  1. GRCh38: Ensembl release 89: ENSG00000178695 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000098557 - Ensembl, 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. Resendes BL, Kuo SF, Robertson NG, Giersch AB, Honrubia D, Ohara O, Adams JC, Morton CC (Sep 2004). "Isolation from cochlea of a novel human intronless gene with predominant fetal expression". J Assoc Res Otolaryngol. 5 (2): 185–202. doi:10.1007/s10162-003-4042-x. PMC 2538407. PMID 15357420.
  6. "Entrez Gene: KCTD12 potassium channel tetramerisation domain containing 12".
  7. Eszlari, Nora; Millinghoffer, Andras; Petschner, Peter; Gonda, Xenia; Baksa, Daniel; Pulay, Attila J.; Réthelyi, János M.; Breen, Gerome; Deakin, John Francis William; Antal, Peter; Bagdy, Gyorgy; Juhasz, Gabriella (2019). "Genome-wide association analysis reveals KCTD12 and miR-383-binding genes in the background of rumination". Translational Psychiatry. 9 (1): 119. doi:10.1038/s41398-019-0454-1. PMC 6423133. PMID 30886212.
  8. "KCTD12 Gene - GeneCards | KCD12 Protein | KCD12 Antibody".

Further reading


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