KCTD12

KCTD12
Identifiers
AliasesKCTD12, C13orf2, PFET1, PFETIN, potassium channel tetramerization domain containing 12
External IDsOMIM: 610521; MGI: 2145823; HomoloGene: 16316; GeneCards: KCTD12; OMA:KCTD12 - orthologs
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

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

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

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000178695 – Ensembl, May 2017
  2. ^ a b c 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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