NSUN4
5-cytosine rRNA methyltransferase NSUN4
Also known as: MGC22960, NSUN4_HUMAN, SHTAP
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96CB9
- Gene
- NSUN4
- Ensembl
- ENSG00000117481
- Chromosome
- 1
- Canonical length
- 384 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Enables mRNA (cytidine-5-)-methyltransferase activity and rRNA (cytosine-C5-)-methyltransferase activity. Involved in mitochondrial RNA catabolic process; mitochondrial RNA modification; and rRNA methylation. Located in mitochondrial matrix. Part of mitochondrial large ribosomal subunit. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
384 residues, UniProt reviewed canonical sequence.
>Q96CB9|NSUN4
1 MAALTLRGVR ELLKRVDLAT VPRRHRYKKK WAATEPKFPA VRLALQNFDM TYSVQFGDLW
61 PSIRVSLLSE QKYGALVNNF AAWDHVSAKL EQLSAKDFVN EAISHWELQS EGGQSAAPSP
121 ASWACSPNLR CFTFDRGDIS RFPPARPGSL GVMEYYLMDA ASLLPVLALG LQPGDIVLDL
181 CAAPGGKTLA LLQTGCCRNL AANDLSPSRI ARLQKILHSY VPEEIRDGNQ VRVTSWDGRK
241 WGELEGDTYD RVLVDVPCTT DRHSLHEEEN NIFKRSRKKE RQILPVLQVQ LLAAGLLATK
301 PGGHVVYSTC SLSHLQNEYV VQGAIELLAN QYSIQVQVED LTHFRRVFMD TFCFFSSCQV
361 GELVIPNLMA NFGPMYFCKM RRLTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against NSUN4 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)
- 0.28
- Highest tissue expression
- 80 nTPM
Expression across tissuesHPA
Tissue
- testis: 80 nTPM
- parathyroid gland: 7.6 nTPM
- tongue: 6.5 nTPM
- skeletal muscle: 6.4 nTPM
- thyroid gland: 6.3 nTPM
- liver: 6.2 nTPM
Single-cell type
- late spermatids: 922 nCPM
- early spermatids: 167 nCPM
- epicardial cells: 71 nCPM
- neutrophils: 61 nCPM
- late primary spermatocytes: 50 nCPM
- proximal tubule cells: 43 nCPM
Immune cell
- memory B-cell: 5 nTPM
- myeloid DC: 4.9 nTPM
- plasmacytoid DC: 4.4 nTPM
- classical monocyte: 4.1 nTPM
- eosinophil: 4 nTPM
- naive CD4 T-cell: 3.6 nTPM
Brain region
- pons: 15 nTPM
- white matter: 14 nTPM
- choroid plexus: 14 nTPM
- hypothalamus: 13 nTPM
- midbrain: 13 nTPM
- thalamus: 13 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)
- 0.91
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.83
- DepMap mean gene effect
- -0.39
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- mitochondrial large ribosomal subunit assembly
- mitochondrial RNA catabolic process
- rRNA methylation
- mitochondrial RNA modification
Molecular functions
- methyltransferase activity
- mitochondrial ribosomal large subunit rRNA binding
- mRNA (cytidine-5-)-methyltransferase activity
- RNA methyltransferase activity
- rRNA (cytosine-C5-)-methyltransferase activity
- rRNA methyltransferase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of NSUN4 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 NSUN4 as an antibody target. Whether an autoantibody or antibody against NSUN4 could matter depends on whether native NSUN4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NSUN4 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 NSUN4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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