Zinc finger homeobox 2: Difference between revisions

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{{Infobox_gene}}
{{Infobox_gene}}
 
'''Zinc finger homeobox 2''' is a [[protein]] that in humans is encoded by the ZFHX2 [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: Zinc finger homeobox 2 | url = https://www.ncbi.nlm.nih.gov/gene/85446 }}</ref> It has been implicated in [[Congenital insensitivity to pain|pain insensitivity]].<ref name="HabibMatsuyama2017" />
'''Zinc finger homeobox 2''' is a [[protein]] that in humans is encoded by the ZFHX2 [[gene]].
<ref name="entrez">
{{cite web
| title = Entrez Gene: Zinc finger homeobox 2
| url = https://www.ncbi.nlm.nih.gov/gene/85446
| accessdate = 2016-02-25
}}</ref>


== References ==
== References ==
 
{{reflist|refs =
{{reflist}}
<ref name="HabibMatsuyama2017">{{cite journal | vauthors = Habib AM, Matsuyama A, Okorokov AL, Santana-Varela S, Bras JT, Aloisi AM, Emery EC, Bogdanov YD, Follenfant M, Gossage SJ, Gras M, Humphrey J, Kolesnikov A, Le Cann K, Li S, Minett MS, Pereira V, Ponsolles C, Sikandar S, Torres JM, Yamaoka K, Zhao J, Komine Y, Yamamori T, Maniatis N, Panov KI, Houlden H, Ramirez JD, Bennett DL, Marsili L, Bachiocco V, Wood JN, Cox JJ | display-authors = 6 | title = A novel human pain insensitivity disorder caused by a point mutation in ZFHX2 | journal = Brain | date = December 2017 | pmid = 29253101 | doi = 10.1093/brain/awx326 }}</ref>
 
}}
== Further reading ==
 
{{refbegin | 2}}
 
{{refend}}


[[Category:Human proteins]]
[[Category:Human proteins]]


{{gene-14-stub}}
{{gene-14-stub}}

Latest revision as of 06:31, 10 January 2019

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez

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Ensembl

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UniProt

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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

Zinc finger homeobox 2 is a protein that in humans is encoded by the ZFHX2 gene.[1] It has been implicated in pain insensitivity.[2]

References

  1. ↑ "Entrez Gene: Zinc finger homeobox 2".
  2. ↑ Habib AM, Matsuyama A, Okorokov AL, Santana-Varela S, Bras JT, Aloisi AM, et al. (December 2017). "A novel human pain insensitivity disorder caused by a point mutation in ZFHX2". Brain. doi:10.1093/brain/awx326. PMID 29253101.
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