Gene
TRAPPC2
trafficking protein particle complex subunit 2
- HGNC 23068↗(opens in a new tab)
- Ensembl gene ENSG00000196459↗(opens in a new tab)
- NCBI Gene 6399↗(opens in a new tab)
Summary
- Cytogenetic location
- Xp22.2
- Coordinates
- Chromosome X: 13,712,245–13,734,620 (GRCh38)
- Exons
- 6 exons across 22.4 kb
- Protein
- 140 amino acids
- Also known as
- TRS20, SEDT, MIP-2A, ZNF547L, hYP38334
- Previous symbols
- SEDL
- MANE Select transcript
- ENST00000380579.6NM_001011658.4
- 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.
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No Genome Test report reads TRAPPC2 yet. The test sequences your whole genome, so your data includes it all the same.
How TRAPPC2 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 2.8 kb of the gene's 22.4 kb; 423 of those bases code for the protein.
How a genome test reads TRAPPC2
10
positions in TRAPPC2 where ClinVar classes a change as pathogenic or likely pathogenic
2 of them (20%) fall in regions short reads find hard.
- Low mappability (1 site)Regions where 100 bp or 250 bp reads cannot be placed uniquely.
- Segmental duplications (1 site)Copies of at least 1 kb sharing at least 90% identity with another part of the genome (paralogues, pseudogenes); reads may align to the wrong copy.
A whole genome covers all 22.4 kb of TRAPPC2, introns included, not only the 2.8 kb of exons.
Traits linked to TRAPPC2
The Human Phenotype Ontology lists these as features of the rare conditions TRAPPC2 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the musculoskeletal system
- Back pain
- Barrel-shaped chest
- Flattened vertebrae
- Hump-shaped mound of bone in central and posterior portions of vertebral endplate
- Disproportionate short-trunked short stature
- Multiple epiphyseal dysplasia
- Multiple skeletal anomalies
- Premature osteoarthritis
Show 28 more traits
- Abnormal bone maturation of vertebra
- Abnormal lumbar spine morphology
- Abnormal maturation of the end part of a bone
- Abnormal shape of cartilage
- Abnormality of the shoulder
- Hip joint pain
- Hip osteoarthritis
- Increased bone mineral density
- Intervertebral space narrowing
- Knee pain
- Limitation of joint mobility
- Biconcave vertebral bodies
- Excessive inward curvature of lower spine
- Hypoplasia of the odontoid process
- Kyphoscoliosis
- Limb pain
- Limited neck movement
- Limited shoulder movement
- Localized osteoporosis
- Scoliosis
- Stiff knee
- Thoracic kyphosis
- Hunched back
- Hypoplastic iliac wing
- Irregular end part of long bone
- Shield chest
- Spondyloepiphyseal dysplasia
- Synovitis
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 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.). TRAPPC2 gene: trafficking protein particle complex subunit 2. Retrieved 16 October 2026, from https://dantelabs.com/genes/trappc2
Dante Labs. TRAPPC2 gene: trafficking protein particle complex subunit 2 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/trappc2
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