KDM3A: Difference between revisions

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{{Infobox_gene}}
{{Infobox_gene}}
'''Lysine demethylase 3A''' is a [[protein]] that in humans is encoded by the KDM3A [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: Lysine demethylase 3A | url = https://www.ncbi.nlm.nih.gov/gene/55818 }}</ref>
'''Lysine demethylase 3A''' is a [[protein]] that in humans is encoded by the KDM3A [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: Lysine demethylase 3A | url = https://www.ncbi.nlm.nih.gov/gene/55818 }}</ref>
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== Function ==
== Function ==


This gene encodes a zinc finger protein that contains a jumonji domain and may play a role in hormone-dependent transcriptional activation. Alternative splicing results in multiple transcript variants.
This gene encodes a [[zinc finger]] protein that contains a jumonji domain and may play a role in hormone-dependent [[Transcription (biology)|transcriptional]] activation. [[Alternative splicing]] results in multiple transcript variants.


== References ==
== References ==

Latest revision as of 13:49, 19 February 2018

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

n/a

n/a

RefSeq (protein)

n/a

n/a

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

Lysine demethylase 3A is a protein that in humans is encoded by the KDM3A gene.[1]

Function

This gene encodes a zinc finger protein that contains a jumonji domain and may play a role in hormone-dependent transcriptional activation. Alternative splicing results in multiple transcript variants.

References

  1. "Entrez Gene: Lysine demethylase 3A".

Further reading

  • Wellmann S, Bettkober M, Zelmer A, Seeger K, Faigle M, Eltzschig HK, Bührer C (2008). "Hypoxia upregulates the histone demethylase JMJD1A via HIF-1". Biochem. Biophys. Res. Commun. 372 (4): 892–7. doi:10.1016/j.bbrc.2008.05.150. PMID 18538129.

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