KDM3A

Lysine demethylase 3A is a protein that in humans is encoded by the KDM3A gene.[5]

KDM3A
Identifiers
AliasesKDM3A, JHDM2A, JHMD2A, JMJD1, JMJD1A, TSGA, lysine demethylase 3A
External IDsOMIM: 611512 MGI: 98847 HomoloGene: 10196 GeneCards: KDM3A
Gene location (Human)
Chr.Chromosome 2 (human)[1]
Band2p11.2Start86,440,647 bp[1]
End86,492,716 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

55818

104263

Ensembl

ENSG00000115548

ENSMUSG00000053470

UniProt

Q9Y4C1

Q6PCM1

RefSeq (mRNA)

NM_001146688
NM_018433

NM_001038695
NM_173001
NM_001362200
NM_001362201

RefSeq (protein)

NP_001140160
NP_060903

NP_001033784
NP_766589
NP_001349129
NP_001349130

Location (UCSC)Chr 2: 86.44 – 86.49 MbChr 6: 71.59 – 71.63 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

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. GRCh38: Ensembl release 89: ENSG00000115548 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000053470 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "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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