Gene
TNPO3
transportin 3
- HGNC 17103↗(opens in a new tab)
- Ensembl gene ENSG00000064419↗(opens in a new tab)
- NCBI Gene 23534↗(opens in a new tab)
Summary
- Cytogenetic location
- 7q32.1
- Coordinates
- Chromosome 7: 128,954,185–129,055,111 (GRCh38)
- Exons
- 23 exons across 100.9 kb
- Protein
- 923 amino acids
- Also known as
- TRN-SR, MTR10A, TRN-SR2, IPO12
- Previous symbols
- LGMD1F
- MANE Select transcript
- ENST00000265388.10NM_012470.4
- 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 TNPO3, 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
Limb-Girdle Muscular Dystrophy
Limb-girdle Muscular Dystrophy is defined as a collection of numerous subtypes with differing inheritance patterns (with diagnostic sufficiency being varied too). Carriers of variants related to the condition should seek guidance from a muscular-skeletal specialist for a definitive diagnosis.
- ClinGen rates the link definitive
- 3 GenCC submitters rate it definitive or strong
How TNPO3 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 4.3 kb of the gene's 100.9 kb; 2,772 of those bases code for the protein.
How a genome test reads TNPO3
5
positions in TNPO3 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 100.9 kb of TNPO3, introns included, not only the 4.3 kb of exons.
Genes linked to the same conditions
- ANO5anoctamin 5Shares 1 condition
- CAPN3calpain 3Shares 1 condition
- COL6A1collagen type VI alpha 1 chainShares 1 condition
- COL6A2collagen type VI alpha 2 chainShares 1 condition
- COL6A3collagen type VI alpha 3 chainShares 1 condition
- DAG1dystroglycan 1Shares 1 condition
- DNAJB6DnaJ heat shock protein family (Hsp40) member B6Shares 1 condition
- DYSFdysferlinShares 1 condition
- FKRPfukutin related proteinShares 1 condition
- FKTNfukutinShares 1 condition
- GMPPBGDP-mannose pyrophosphorylase BShares 1 condition
- HMGCR3-hydroxy-3-methylglutaryl-CoA reductaseShares 1 condition
Traits linked to TNPO3
The Human Phenotype Ontology lists these as features of the rare conditions TNPO3 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.). TNPO3 gene: transportin 3. Retrieved 16 October 2026, from https://dantelabs.com/genes/tnpo3
Dante Labs. TNPO3 gene: transportin 3 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/tnpo3
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks