Seroatlas · Human Serome Atlas

EEF1AKMT4

EEF1A lysine methyltransferase 4

Also known as: EFMT4_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
P0DPD7
Gene
EEF1AKMT4
Ensembl
ENSG00000284753
Chromosome
3
Canonical length
255 aa
Protein class
Predicted intracellular proteins
Subcellular location
Nucleoplasm,Cytosol

OverviewNCBI Gene

This gene encodes a member of the lysine-specific methyltransferase (KMT) family. The encoded enzyme catalyzes the methylation of lysine-36 of the eukaryotic translation elongation factor 1 alpha. Methylation by this enzyme may affect endoplasmic reticulum-related processes. [provided by RefSeq, Jul 2017]

Canonical amino-acid sequenceUniProt

255 residues, UniProt reviewed canonical sequence.

>P0DPD7|EEF1AKMT4
     1  MASPGAGRAP PELPERNCGY REVEYWDQRY QGAADSAPYD WFGDFSSFRA LLEPELRPED
    61  RILVLGCGNS ALSYELFLGG FPNVTSVDYS SVVVAAMQAR HAHVPQLRWE TMDVRKLDFP
   121  SASFDVVLEK GTLDALLAGE RDPWTVSSEG VHTVDQVLSE VSRVLVPGGR FISMTSAAPH
   181  FRTRHYAQAY YGWSLRHATY GSGFHFHLYL MHKGGKLSVA QLALGAQILS PPRPPTSPCF
   241  LQDSDHEDFL SAIQL

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against EEF1AKMT4 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
Unknown
Secreted
No
Transmembrane segments
0
Mean surface accessibility (rSASA)
0.31
Highest tissue expression
23 nTPM

Expression across tissuesHPA

Tissue

  • liver: 23 nTPM
  • testis: 23 nTPM
  • pancreas: 15 nTPM
  • skeletal muscle: 12 nTPM
  • esophagus: 11 nTPM
  • skin: 8.1 nTPM

Single-cell type

  • suprabasal keratinocytes: 5 nCPM
  • late primary spermatocytes: 4.7 nCPM
  • late spermatids: 4.5 nCPM
  • other brain neurons: 4 nCPM
  • basal keratinocytes: 3.5 nCPM
  • early spermatids: 2.6 nCPM

Immune cell

  • classical monocyte: 23 nTPM
  • myeloid DC: 20 nTPM
  • intermediate monocyte: 19 nTPM
  • plasmacytoid DC: 18 nTPM
  • T-reg: 16 nTPM
  • non-classical monocyte: 13 nTPM

Brain region

  • cerebellum: 7.4 nTPM
  • hypothalamus: 2.9 nTPM
  • cerebral cortex: 2.7 nTPM
  • medulla oblongata: 2.4 nTPM
  • pons: 2.1 nTPM
  • choroid plexus: 2 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.

DepMap mean gene effect
-0.06
DepMap dependency class
none

OntologyGO

Biological processes

Molecular functions

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads EEF1AKMT4 as an antibody target. Whether an autoantibody or antibody against EEF1AKMT4 could matter depends on whether native EEF1AKMT4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

EEF1AKMT4 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 EEF1AKMT4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/EEF1AKMT4. 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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