KCTD12: Difference between revisions

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'''BTB/POZ domain-containing protein KCTD12''' is a [[protein]] that in humans is encoded by the ''KCTD12'' [[gene]].<ref name="pmid15357420">{{cite journal |vauthors=Resendes BL, Kuo SF, Robertson NG, Giersch AB, Honrubia D, Ohara O, Adams JC, Morton CC | title = Isolation from cochlea of a novel human intronless gene with predominant fetal expression | journal = J Assoc Res Otolaryngol | volume = 5 | issue = 2 | pages = 185–202 |date=Sep 2004 | pmid = 15357420 | pmc = 2538407 | doi = 10.1007/s10162-003-4042-x }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: KCTD12 potassium channel tetramerisation domain containing 12| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=115207| accessdate = }}</ref>
'''BTB/POZ domain-containing protein KCTD12''' is a [[protein]] that in humans is encoded by the ''KCTD12'' [[gene]].<ref name="pmid15357420">{{cite journal |vauthors=Resendes BL, Kuo SF, Robertson NG, Giersch AB, Honrubia D, Ohara O, Adams JC, Morton CC | title = Isolation from cochlea of a novel human intronless gene with predominant fetal expression | journal = J Assoc Res Otolaryngol | volume = 5 | issue = 2 | pages = 185–202 |date=Sep 2004 | pmid = 15357420 | pmc = 2538407 | doi = 10.1007/s10162-003-4042-x }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: KCTD12 potassium channel tetramerisation domain containing 12| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=115207| accessdate = }}</ref>

Latest revision as of 11:33, 9 January 2019

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

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RefSeq (protein)

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Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

BTB/POZ domain-containing protein KCTD12 is a protein that in humans is encoded by the KCTD12 gene.[1][2]


References

  1. 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.
  2. "Entrez Gene: KCTD12 potassium channel tetramerisation domain containing 12".

Further reading