Gene
EMG1
EMG1 N1-specific pseudouridine methyltransferase
- HGNC 16912↗(opens in a new tab)
- Ensembl gene ENSG00000126749↗(opens in a new tab)
- NCBI Gene 10436↗(opens in a new tab)
Summary
- Cytogenetic location
- 12p13.31
- Coordinates
- Chromosome 12: 6,970,913–6,979,936 (GRCh38)
- Exons
- 6 exons across 9 kb
- Protein
- 244 amino acids
- Also known as
- C2F, NEP1, Grcc2f
- MANE Select transcript
- ENST00000599672.6NM_006331.8
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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How EMG1 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 4.9 kb of the gene's 9 kb; 735 of those bases code for the protein.
Traits linked to EMG1
The Human Phenotype Ontology lists these as features of the rare conditions EMG1 can cause. Each trait's page lists the other genes linked to it.
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
Cite this page
Dante Labs. (n.d.). EMG1 gene: EMG1 N1-specific pseudouridine methyltransferase. Retrieved 16 October 2026, from https://dantelabs.com/genes/emg1
Dante Labs. EMG1 gene: EMG1 N1-specific pseudouridine methyltransferase [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/emg1
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