Gene
PLIN4
perilipin 4
- HGNC 29393↗(opens in a new tab)
- Ensembl gene ENSG00000167676↗(opens in a new tab)
- NCBI Gene 729359↗(opens in a new tab)
Summary
- Cytogenetic location
- 19p13.3
- Coordinates
- Chromosome 19: 4,502,192–4,518,486 (GRCh38)
- Exons
- 8 exons across 16.3 kb
- Protein
- 1,371 amino acids
- Also known as
- S3-12
- Previous symbols
- KIAA1881
- MANE Select transcript
- ENST00000301286.5NM_001367868.2
- Locus type
- Protein-coding
- Very high
- Confident
- Low
- Very low
This page as data
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No Genome Test report reads PLIN4 yet. The test sequences your whole genome, so your data includes it all the same.
How PLIN4 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 6.5 kb of the gene's 16.3 kb; 4,116 of those bases code for the protein.
Sequencing PLIN4
12Moderate
How hard PLIN4 is to sequence with short reads, out of 100Each bar is the share of PLIN4'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.
- MappabilityStretches where 100 or 250 bp reads cannot be placed uniquely, so a call there may be missing or wrong. Weight 35%.3.8%
- 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%.41%
- GC contentWindows under 25% or over 65% G and C, which library preparation covers thinly. Weight 10%.42%
- Reference coverageGaps in the reference assembly nearby, where there is no sequence for reads to align to. Weight 10%.0%
2
positions in PLIN4 where ClinVar classes a change as pathogenic or likely pathogenic
1 of them (50%) falls in a region short reads find hard.
- Low mappabilityRegions where 100 bp or 250 bp reads cannot be placed uniquely. (1 site)
A whole genome covers all 16.3 kb of PLIN4, introns included, not only the 6.5 kb of exons.
Traits linked to PLIN4
The Human Phenotype Ontology lists these as features of the rare conditions PLIN4 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.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- 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.
- Data release 2026.10.17-8666dff2.
Cite this page
Dante Labs. (n.d.). PLIN4 gene: perilipin 4. Retrieved 17 October 2026, from https://dantelabs.com/genes/plin4
Dante Labs. PLIN4 gene: perilipin 4 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/plin4
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