FOXI3

Forkead box I3 (FOXI3) is a protein that in humans is encoded by the FOXI3 gene. FOXI3 is a forkhead box transcription factor that is expressed in the development of hair and teeth. One of its mutations is a dominant allele responsible for the heterozygous Hh hairless trait in dogs. It was identified in 2008.[4]

FOXI3
Identifiers
AliasesFOXI3, forkhead box I3
External IDsOMIM: 612351 MGI: 3511278 HomoloGene: 52949 GeneCards: FOXI3
Gene location (Human)
Chr.Chromosome 2 (human)[1]
Band2p11.2Start88,446,787 bp[1]
End88,452,693 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

344167

232077

Ensembl

ENSG00000214336

n/a

UniProt

A8MTJ6

n/a

RefSeq (mRNA)

NM_001135649

NM_001101464

RefSeq (protein)

NP_001129121

n/a

Location (UCSC)Chr 2: 88.45 – 88.45 Mbn/a
PubMed search[2][3]
Wikidata
View/Edit HumanView/Edit Mouse

See also

References

  1. GRCh38: Ensembl release 89: ENSG00000214336 - Ensembl, May 2017
  2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. Drögemüller C, Karlsson EK, Hytönen MK, Perloski M, Dolf G, Sainio K, et al. (September 2008). "A mutation in hairless dogs implicates FOXI3 in ectodermal development". Science. 321 (5895): 1462. doi:10.1126/science.1162525. PMID 18787161.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.