Identity
HGNC
LOCATION
3q11.2
LOCUSID
ALIAS
COXPD48,MST077,MSTP077
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 63899
MIM: 617491
HGNC: 26208
Ensembl: ENSG00000178694
Variants:
dbSNP: 63899
ClinVar: 63899
TCGA: ENSG00000178694
COSMIC: NSUN3
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000178694 | ENST00000314622 | Q9H649 |
| ENSG00000178694 | ENST00000483378 | F8WF52 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 35997137 | 2024 | RNA 5-Methylcytosine Regulator NSUN3 promotes tumor progression through regulating immune infiltration in head and neck squamous cell carcinoma. | 7 |
| 35997137 | 2024 | RNA 5-Methylcytosine Regulator NSUN3 promotes tumor progression through regulating immune infiltration in head and neck squamous cell carcinoma. | 7 |
| 36949224 | 2023 | NSUN3-mediated mitochondrial tRNA 5-formylcytidine modification is essential for embryonic development and respiratory complexes in mice. | 3 |
| 36949224 | 2023 | NSUN3-mediated mitochondrial tRNA 5-formylcytidine modification is essential for embryonic development and respiratory complexes in mice. | 3 |
| 32488845 | 2020 | Novel Biallelic NSUN3 Variants Cause Early-Onset Mitochondrial Encephalomyopathy and Seizures. | 17 |
| 32488845 | 2020 | Novel Biallelic NSUN3 Variants Cause Early-Onset Mitochondrial Encephalomyopathy and Seizures. | 17 |
| 27214402 | 2016 | NSUN3 methylase initiates 5-formylcytidine biogenesis in human mitochondrial tRNA(Met). | 104 |
| 27497299 | 2016 | NSUN3 and ABH1 modify the wobble position of mt-tRNAMet to expand codon recognition in mitochondrial translation. | 123 |
| 27214402 | 2016 | NSUN3 methylase initiates 5-formylcytidine biogenesis in human mitochondrial tRNA(Met). | 104 |
| 27497299 | 2016 | NSUN3 and ABH1 modify the wobble position of mt-tRNAMet to expand codon recognition in mitochondrial translation. | 123 |
| 19240061 | 2009 | Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling. | 94 |
| 19240061 | 2009 | Coeliac disease-associated risk variants in TNFAIP3 and REL implicate altered NF-kappaB signalling. | 94 |
Citation
Dessen P
NSUN3 (NOP2/Sun RNA methyltransferase 3)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/70990/nsun3-(nop2-sun-rna-methyltransferase-3)
