CSKMT
Citrate synthase-lysine N-methyltransferase CSKMT, mitochondrial
Also known as: CS-KMT, CSKMT_HUMAN, METTL12, U99HG
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A8MUP2
- Gene
- CSKMT
- Ensembl
- ENSG00000214756
- Chromosome
- 11
- Canonical length
- 240 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Enables protein-lysine N-methyltransferase activity. Involved in peptidyl-lysine dimethylation; peptidyl-lysine monomethylation; and peptidyl-lysine trimethylation. Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
240 residues, UniProt reviewed canonical sequence.
>A8MUP2|CSKMT
1 MAALRRMLHL PSLMMGTCRP FAGSLADSCL ADRCLWDRLH AQPRLGTVPT FDWFFGYDEV
61 QGLLLPLLQE AQAASPLRVL DVGCGTSSLC TGLYTKSPHP VDVLGVDFSP VAVAHMNSLL
121 EGGPGQTPLC PGHPASSLHF MHADAQNLGA VASSGSFQLL LDKGTWDAVA RGGLPRAYQL
181 LSECLRVLNP QGTLIQFSDE DPDVRLPCLE QGSYGWTVTV QELGPFRGIT YFAYLIQGSHLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CSKMT 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)
- 0.31
- Highest tissue expression
- 0.9 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 0.9 nTPM
- pancreas: 0.7 nTPM
- ovary: 0.6 nTPM
- cervix: 0.5 nTPM
- duodenum: 0.5 nTPM
- esophagus: 0.5 nTPM
Single-cell type
- colonocytes: 115 nCPM
- breast myoepithelial cells: 79 nCPM
- hepatic stellate cells: 78 nCPM
- breast secretory cells: 69 nCPM
- enterocytes: 67 nCPM
- goblet cells: 59 nCPM
Immune cell
- memory B-cell: 2.7 nTPM
- naive CD4 T-cell: 2.7 nTPM
- naive CD8 T-cell: 2.4 nTPM
- memory CD4 T-cell: 2.3 nTPM
- intermediate monocyte: 1.7 nTPM
- MAIT T-cell: 1.6 nTPM
Brain region
- hypothalamus: 0.2 nTPM
- medulla oblongata: 0.2 nTPM
- thalamus: 0.2 nTPM
- amygdala: 0.1 nTPM
- cerebral cortex: 0.1 nTPM
- choroid plexus: 0.1 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)
- 1.35
- gnomAD pLI
- 0
- DepMap mean gene effect
- -0.19
- 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
- peptidyl-lysine dimethylation
- peptidyl-lysine monomethylation
- peptidyl-lysine trimethylation
- protein methylation
- tricarboxylic acid cycle
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CSKMT as an antibody target. Whether an autoantibody or antibody against CSKMT could matter depends on whether native CSKMT is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CSKMT 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 CSKMT as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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