Seroatlas · Human Serome Atlas

ANTKMT

Adenine nucleotide translocase lysine N-methyltransferase

Also known as: ANKMT_HUMAN, C16orf24, FAM173A, MGC2494

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q9BQD7
Gene
ANTKMT
Ensembl
ENSG00000103254
Chromosome
16
Canonical length
235 aa
Protein class
Predicted intracellular proteins, Predicted membrane proteins
Subcellular location
Cytosol

OverviewNCBI Gene

Enables protein-lysine N-methyltransferase activity. Involved in peptidyl-lysine trimethylation. Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

235 residues, UniProt reviewed canonical sequence.

>Q9BQD7|ANTKMT
     1  MEQDDPVEAL TELRERRLGA LELLQAAAGS GLAAYAVWAL LLQPGFRRVP LRLQVPYVGA
    61  SARQVEHVLS LLRGRPGKTV DLGSGDGRIV LAAHRCGLRP AVGYELNPWL VALARLHAWR
   121  AGCAGSVCYR RKDLWKVSLR DCRNVSVFLA PSVLPLLEDK LRTELPAGAR VVSGRFPLPT
   181  WQPVTAVGEG LDRVWAYDVP EGGQAGEAAS SRIPIQAAPG PSSAPIPGGL ISQAS

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against ANTKMT 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
Other membrane
Secreted
No
Transmembrane segments
1
Mean surface accessibility (rSASA)
0.39
Highest tissue expression
42 nTPM

Expression across tissuesHPA

Tissue

  • liver: 42 nTPM
  • kidney: 37 nTPM
  • amygdala: 37 nTPM
  • cerebral cortex: 35 nTPM
  • hippocampal formation: 34 nTPM
  • pituitary gland: 31 nTPM

Single-cell type

  • late spermatids: 785 nCPM
  • late primary spermatocytes: 424 nCPM
  • early spermatids: 217 nCPM
  • enterocytes: 154 nCPM
  • esophageal suprabasal cells: 118 nCPM
  • colonocytes: 117 nCPM

Immune cell

  • naive CD8 T-cell: 27 nTPM
  • MAIT T-cell: 25 nTPM
  • T-reg: 23 nTPM
  • naive B-cell: 22 nTPM
  • memory CD8 T-cell: 20 nTPM
  • memory B-cell: 18 nTPM

Brain region

  • medulla oblongata: 33 nTPM
  • midbrain: 29 nTPM
  • white matter: 28 nTPM
  • thalamus: 26 nTPM
  • cerebral cortex: 26 nTPM
  • spinal cord: 26 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)
1.62
gnomAD pLI
0
DepMap mean gene effect
-0.01
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

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads ANTKMT as an antibody target. Whether an autoantibody or antibody against ANTKMT could matter depends on whether native ANTKMT is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

ANTKMT 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 ANTKMT as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/ANTKMT. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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