KDM4A
Lysine-specific demethylase 4A
Also known as: JHDM3A, JMJD2, JMJD2A, KDM4A_HUMAN, KIAA0677, TDRD14A
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75164
- Gene
- KDM4A
- Ensembl
- ENSG00000066135
- Chromosome
- 1
- Canonical length
- 1064 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli fibrillar center
OverviewNCBI Gene
This gene is a member of the Jumonji domain 2 (JMJD2) family and encodes a protein containing a JmjN domain, a JmjC domain, a JD2H domain, two TUDOR domains, and two PHD-type zinc fingers. This nuclear protein functions as a trimethylation-specific demethylase, converting specific trimethylated histone residues to the dimethylated form, and as a transcriptional repressor. [provided by RefSeq, Apr 2009]
Canonical amino-acid sequenceUniProt
1064 residues, UniProt reviewed canonical sequence.
>O75164|KDM4A
1 MASESETLNP SARIMTFYPT MEEFRNFSRY IAYIESQGAH RAGLAKVVPP KEWKPRASYD
61 DIDDLVIPAP IQQLVTGQSG LFTQYNIQKK AMTVREFRKI ANSDKYCTPR YSEFEELERK
121 YWKNLTFNPP IYGADVNGTL YEKHVDEWNI GRLRTILDLV EKESGITIEG VNTPYLYFGM
181 WKTSFAWHTE DMDLYSINYL HFGEPKSWYS VPPEHGKRLE RLAKGFFPGS AQSCEAFLRH
241 KMTLISPLML KKYGIPFDKV TQEAGEFMIT FPYGYHAGFN HGFNCAESTN FATRRWIEYG
301 KQAVLCSCRK DMVKISMDVF VRKFQPERYK LWKAGKDNTV IDHTLPTPEA AEFLKESELP
361 PRAGNEEECP EEDMEGVEDG EEGDLKTSLA KHRIGTKRHR VCLEIPQEVS QSELFPKEDL
421 SSEQYEMTEC PAALAPVRPT HSSVRQVEDG LTFPDYSDST EVKFEELKNV KLEEEDEEEE
481 QAAAALDLSV NPASVGGRLV FSGSKKKSSS SLGSGSSRDS ISSDSETSEP LSCRAQGQTG
541 VLTVHSYAKG DGRVTVGEPC TRKKGSAARS FSERELAEVA DEYMFSLEEN KKSKGRRQPL
601 SKLPRHHPLV LQECVSDDET SEQLTPEEEA EETEAWAKPL SQLWQNRPPN FEAEKEFNET
661 MAQQAPHCAV CMIFQTYHQV EFGGFNQNCG NASDLAPQKQ RTKPLIPEMC FTSTGCSTDI
721 NLSTPYLEED GTSILVSCKK CSVRVHASCY GVPPAKASED WMCSRCSANA LEEDCCLCSL
781 RGGALQRAND DRWVHVSCAV AILEARFVNI AERSPVDVSK IPLPRFKLKC IFCKKRRKRT
841 AGCCVQCSHG RCPTAFHVSC AQAAGVMMQP DDWPFVVFIT CFRHKIPNLE RAKGALQSIT
901 AGQKVISKHK NGRFYQCEVV RLTTETFYEV NFDDGSFSDN LYPEDIVSQD CLQFGPPAEG
961 EVVQVRWTDG QVYGAKFVAS HPIQMYQVEF EDGSQLVVKR DDVYTLDEEL PKRVKSRLSV
1021 ASDMRFNEIF TEKEVKQEKK RQRVINSRYR EDYIEPALYR AIMELocalizationUniProt · AlphaFold · HPA
Whether an antibody against KDM4A can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.39
- Highest tissue expression
- 26 nTPM
Expression across tissuesHPA
Tissue
- duodenum: 26 nTPM
- small intestine: 21 nTPM
- skin: 21 nTPM
- thymus: 20 nTPM
- adrenal gland: 19 nTPM
- ovary: 19 nTPM
Single-cell type
- choroid plexus epithelial cells: 39 nCPM
- ependymal cells: 36 nCPM
- oligodendrocytes: 35 nCPM
- brain inhibitory neurons: 31 nCPM
- microglia: 31 nCPM
- oligodendrocyte progenitor cells: 29 nCPM
Immune cell
- basophil: 10 nTPM
- eosinophil: 9 nTPM
- non-classical monocyte: 5.2 nTPM
- MAIT T-cell: 5 nTPM
- classical monocyte: 4.9 nTPM
- T-reg: 4.9 nTPM
Brain region
- cerebellum: 27 nTPM
- cerebral cortex: 26 nTPM
- choroid plexus: 26 nTPM
- basal ganglia: 24 nTPM
- pons: 23 nTPM
- white matter: 23 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.16
- gnomAD pLI
- 1
- gnomAD missense Z
- 3.68
- DepMap mean gene effect
- -0.13
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cardiac muscle hypertrophy in response to stress
- chromatin remodeling
- negative regulation of autophagy
- negative regulation of DNA-templated transcription
- negative regulation of gene expression
- regulation of gene expression
Molecular functions
- histone demethylase activity
- histone H3K36 demethylase activity
- histone H3K9 demethylase activity
- histone H3K9me2/H3K9me3 demethylase activity
- histone H4K20me2 reader activity
- ubiquitin protein ligase binding
- zinc ion binding
- histone H3K36me2/H3K36me3 demethylase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Zinc finger, PHD-type
- Tudor domain
- JmjC domain
- JmjN domain
- Zinc finger, FYVE/PHD-type
- Zinc finger, RING/FYVE/PHD-type
- Zinc finger, PHD-finger
- Extended PHD (ePHD) domain
- Lysine-specific demethylase 4-like, Tudor domain
- JmjC domain, hydroxylase
- jmjN domain
- PHD-finger
- PHD-zinc-finger like domain
- Jumonji domain-containing protein 2A Tudor domain
- Lysine-specific demethylase 4A, first Tudor domain
- Lysine-specific demethylase 4A, second Tudor domain
- Lysine-specific demethylase 4A, extended PHD finger
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of KDM4A in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads KDM4A as an antibody target. Whether an autoantibody or antibody against KDM4A could matter depends on whether native KDM4A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KDM4A is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label KDM4A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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