KDM3A

KDM3A
Identifiers
Aliases KDM3A, JHDM2A, JHMD2A, JMJD1, JMJD1A, TSGA, lysine demethylase 3A
External IDs MGI: 98847 HomoloGene: 10196 GeneCards: KDM3A
Orthologs
Species Human Mouse
Entrez

55818

104263

Ensembl

ENSG00000115548

ENSMUSG00000053470

UniProt

Q9Y4C1

Q6PCM1

RefSeq (mRNA)

NM_001146688
NM_018433

NM_001038695
NM_173001

RefSeq (protein)

NP_001140160.1
NP_060903.2

NP_001033784.2
NP_766589.1

Location (UCSC) Chr 2: 86.44 – 86.49 Mb Chr 6: 71.59 – 71.63 Mb
PubMed search [1] [2]
Wikidata
View/Edit HumanView/Edit Mouse

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

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. ↑ "Human PubMed Reference:".
  2. ↑ "Mouse PubMed Reference:".
  3. ↑ "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.


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