KDM8

Protein-coding gene in the species Homo sapiens
KDM8
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

3UYJ, 4AAP, 4GAZ, 4GJY, 4GJZ, 4QU1

Identifiers
AliasesKDM8, JMJD5, lysine demethylase 8
External IDsOMIM: 611917; MGI: 1924285; HomoloGene: 49791; GeneCards: KDM8; OMA:KDM8 - orthologs
Gene location (Human)
Chromosome 16 (human)
Chr.Chromosome 16 (human)[1]
Chromosome 16 (human)
Genomic location for KDM8
Genomic location for KDM8
Band16p12.1Start27,203,508 bp[1]
End27,221,768 bp[1]
Gene location (Mouse)
Chromosome 7 (mouse)
Chr.Chromosome 7 (mouse)[2]
Chromosome 7 (mouse)
Genomic location for KDM8
Genomic location for KDM8
Band7|7 F3Start125,043,848 bp[2]
End125,061,441 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • right lobe of liver

  • duodenum

  • testicle

  • gonad

  • granulocyte

  • apex of heart

  • epithelium of colon

  • body of pancreas

  • prefrontal cortex

  • mucosa of transverse colon
Top expressed in
  • retinal pigment epithelium

  • primitive streak

  • cumulus cell

  • neural layer of retina

  • embryo

  • morula

  • secondary oocyte

  • ventricular zone

  • triceps brachii muscle

  • Rostral migratory stream
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
  • dioxygenase activity
  • chromatin binding
  • oxidoreductase activity
  • metal ion binding
  • histone H3-methyl-lysine-36 demethylase activity
  • histone demethylase activity
  • protein binding
  • peptidase activity
  • hydrolase activity
  • aminopeptidase activity
  • endopeptidase activity
  • 2-oxoglutarate-dependent dioxygenase activity
  • methylated histone binding
Cellular component
  • nucleus
  • nucleoplasm
  • cytosol
  • chromosome
Biological process
  • regulation of transcription, DNA-templated
  • cell cycle
  • G2/M transition of mitotic cell cycle
  • positive regulation of transcription, DNA-templated
  • histone H3-K36 demethylation
  • transcription, DNA-templated
  • proteolysis
  • chromatin organization
  • protein destabilization
  • circadian regulation of gene expression
  • negative regulation of transcription, DNA-templated
  • rhythmic process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

79831

77035

Ensembl

ENSG00000155666

ENSMUSG00000030752

UniProt

Q8N371

Q9CXT6

RefSeq (mRNA)

NM_001145348
NM_024773

NM_029842

RefSeq (protein)

NP_001138820
NP_079049

NP_084118

Location (UCSC)Chr 16: 27.2 – 27.22 MbChr 7: 125.04 – 125.06 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Lysine demethylase 8 is a protein that in humans is encoded by the KDM8 gene.[5]

Function

This gene likely encodes a histone lysine demethylase. Studies of a similar protein in mouse indicate a potential role for this protein as a tumor suppressor. Alternatively spliced transcript variants have been described.

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000155666 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000030752 – 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 8". Retrieved 2016-04-09.

Further reading

  • Suzuki T, Minehata K, Akagi K, Jenkins NA, Copeland NG (2006). "Tumor suppressor gene identification using retroviral insertional mutagenesis in Blm-deficient mice". EMBO J. 25 (14): 3422–31. doi:10.1038/sj.emboj.7601215. PMC 1523184. PMID 16858412.

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


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