OTX1

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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

Homeobox protein OTX1 is a protein that in humans is encoded by the OTX1 gene.[1][2]

Function

This gene encodes a member of the bicoid sub-family of homeodomain-containing transcription factors. The encoded protein acts as a transcription factor and may play a role in brain and sensory organ development. The Otx gene is active in the region of the first gill arch, which is related to the upper and lower jaw and two of the bones of the ear.[3] A similar protein in mice is required for proper brain and sensory organ development and can cause epilepsy.[2]

References

  1. Kastury K, Druck T, Huebner K, Barletta C, Acampora D, Simeone A, Faiella A, Boncinelli E (July 1994). "Chromosome locations of human EMX and OTX genes". Genomics. 22 (1): 41–5. doi:10.1006/geno.1994.1343. PMID 7959790.
  2. 2.0 2.1 "Entrez Gene: OTX1 orthodenticle homeobox 1".
  3. Shubin, Neil "Your Inner Fish" 2009

Further reading

External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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