Gene
SNRPE
small nuclear ribonucleoprotein polypeptide E
- HGNC 11161↗(opens in a new tab)
- Ensembl gene ENSG00000182004↗(opens in a new tab)
- NCBI Gene 6635↗(opens in a new tab)
Summary
- Cytogenetic location
- 1q32.1
- Coordinates
- Chromosome 1: 203,861,599–203,871,152 (GRCh38)
- Exons
- 5 exons across 9.6 kb
- Protein
- 92 amino acids
- Also known as
- Sm-E
- MANE Select transcript
- ENST00000414487.7NM_003094.4
- 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.
Read SNRPE, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome TestCurated report relevant to this gene
Hereditary Hypotrichosis, Woolly Hair and Monilethrix
- Hereditary hypotrichosis
Sparse or absent scalp and body hair from childhood, including the LIPH- and LPAR6-related forms.
- 3 GenCC submitters rate it definitive or strong
How SNRPE is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- 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 1.6 kb of the gene's 9.6 kb; 279 of those bases code for the protein.
How a genome test reads SNRPE
1
position in SNRPE where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
A whole genome covers all 9.6 kb of SNRPE, introns included, not only the 1.6 kb of exons.
Genes linked to the same conditions
- APCDD1APC down-regulated 1Shares 1 condition
- C3orf52chromosome 3 open reading frame 52Shares 1 condition
- CDH3cadherin 3Shares 1 condition
- CDSNcorneodesmosinShares 1 condition
- DSG4desmoglein 4Shares 1 condition
- HRHR lysine demethylase and nuclear receptor corepressorShares 1 condition
- LIPHlipase HShares 1 condition
- LPAR6lysophosphatidic acid receptor 6Shares 1 condition
- LSSlanosterol synthaseShares 1 condition
- RPL21ribosomal protein L21Shares 1 condition
Traits linked to SNRPE
The Human Phenotype Ontology lists these as features of the rare conditions SNRPE 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.
- GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). SNRPE gene: small nuclear ribonucleoprotein polypeptide E. Retrieved 16 October 2026, from https://dantelabs.com/genes/snrpe
Dante Labs. SNRPE gene: small nuclear ribonucleoprotein polypeptide E [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/snrpe
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks