Gene
TXNRD2
thioredoxin reductase 2
- HGNC 18155↗(opens in a new tab)
- Ensembl gene ENSG00000184470↗(opens in a new tab)
- NCBI Gene 10587↗(opens in a new tab)
Summary
- Cytogenetic location
- 22q11.21
- Coordinates
- Chromosome 22: 19,875,522–19,941,818 (GRCh38)
- Exons
- 18 exons across 66.3 kb
- Protein
- 524 amino acids
- Inheritance
- Autosomal recessive
- Also known as
- TR, TRXR2, TR3, SELZ, TXNR2
- MANE Select transcript
- ENST00000400521.7NM_006440.5
- Locus type
- gene with protein product
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Familial Glucocorticoid Deficiency
- Autosomal recessive
- 1 GenCC submitter rates it definitive or strong
Inheritance
- Autosomal recessive
- It takes a changed copy from each parent. With one, you are a carrier and usually unaffected; when both parents are carriers, each child has a one-in-four chance of inheriting two.
How TXNRD2 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 1.9 kb of the gene's 66.3 kb; 1,575 of those bases code for the protein.
How a genome test reads TXNRD2
1
position in TXNRD2 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 66.3 kb of TXNRD2, introns included, not only the 1.9 kb of exons.
Genes linked to the same conditions
Traits linked to TXNRD2
The Human Phenotype Ontology lists these as features of the rare conditions TXNRD2 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the endocrine system
- Adrenal insufficiency
- Low blood cortisol level
- Abnormal circulating adrenocorticotropin concentration
- Decreased circulating dehydroepiandrosterone concentration
- Impaired cortisol response to insulin stimulation test
- Early onset of puberty
- Low blood aldosterone level
- Underactive thyroid gland from birth
Show 1 more trait
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.). TXNRD2 gene: thioredoxin reductase 2. Retrieved 16 October 2026, from https://dantelabs.com/genes/txnrd2
Dante Labs. TXNRD2 gene: thioredoxin reductase 2 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/txnrd2
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