Gene
PRRX1
paired related homeobox 1
- HGNC 9142↗(opens in a new tab)
- Ensembl gene ENSG00000116132↗(opens in a new tab)
- NCBI Gene 5396↗(opens in a new tab)
Summary
- Cytogenetic location
- 1q24.2
- Coordinates
- Chromosome 1: 170,664,131–170,739,421 (GRCh38)
- Exons
- 4 exons across 75.3 kb
- Protein
- 245 amino acids
- Also known as
- PHOX1
- Previous symbols
- PMX1
- MANE Select transcript
- ENST00000239461.11NM_022716.4
- Locus type
- Protein-coding
- Very high
- Confident
- Low
- Very low
This page as data
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How PRRX1 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 4.1 kb of the gene's 75.3 kb; 738 of those bases code for the protein.
Sequencing PRRX1
2Easy
How hard PRRX1 is to sequence with short reads, out of 100
0 · Easy100 · Hard
Almost all of PRRX1's exons sit where short reads map cleanly.
What adds to it: the share of PRRX1's exons in each kind of hard region
- MappabilityStretches where 100 or 250 bp reads cannot be placed uniquely, so a call there may be missing or wrong. Weight 35%.0%
- HomologySegmental duplications: copies elsewhere in the genome, such as paralogues and pseudogenes, at 90% identity or more. Weight 30%.0%
- RepeatsTandem repeats and runs of one base, which reads slip on and may not span. Weight 15%.6.6%
- GC contentWindows under 25% or over 65% G and C, which library preparation covers thinly. Weight 10%.8.1%
- Reference coverageGaps in the reference assembly nearby, where there is no sequence for reads to align to. Weight 10%.0%
A Dante Labs score from our own research, built on NIST's Genome in a Bottle maps of hard-to-sequence regions.How it's scoredEach bar is the share of PRRX1's exon bases in that kind of difficult region. The score weighs them by how much each costs a short-read call: 0 when no base is in any, 100 when every base is in all of them.
Traits linked to PRRX1
The Human Phenotype Ontology lists these as features of the rare conditions PRRX1 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 Genome in a Bottle genome stratifications, from NIST: the sequencing difficulty score.
- 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.). PRRX1 gene: paired related homeobox 1. Retrieved 18 October 2026, from https://dantelabs.com/genes/prrx1
Dante Labs. PRRX1 gene: paired related homeobox 1 [Internet]. [cited 18 October 2026]. Available from: https://dantelabs.com/genes/prrx1
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