TXN (thioredoxin)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 7295 |
| Gene name | Thioredoxin |
| Gene symbol | TXN |
| Synonyms (NCBI Gene) |
TRDXTRXTRX1TXN1Trx80
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| Chromosome | 9 |
| Chromosome location | 9q31.3 |
| Summary | The protein encoded by this gene acts as a homodimer and is involved in many redox reactions. The encoded protein is active in the reversible S-nitrosylation of cysteines in certain proteins, which is part of the response to intracellular nitric oxide. Th |
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miRNA
miRNA information provided by mirtarbase database.
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Transcription factors
Transcription factors information provided by TRRUST V2 database.
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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P10599 | ||||||||||
| Protein name | Thioredoxin (Trx) (ATL-derived factor) (ADF) (Surface-associated sulphydryl protein) (SASP) (allergen Hom s Trx) | ||||||||||
| Protein function | Participates in various redox reactions through the reversible oxidation of its active center dithiol to a disulfide and catalyzes dithiol-disulfide exchange reactions (PubMed:17182577, PubMed:19032234, PubMed:2176490). Plays a role in the rever | ||||||||||
| PDB | 1AIU , 1AUC , 1CQG , 1CQH , 1ERT , 1ERU , 1ERV , 1ERW , 1M7T , 1MDI , 1MDJ , 1MDK , 1TRS , 1TRU , 1TRV , 1TRW , 2HSH , 2HXK , 2IFQ , 2IIY , 3E3E , 3KD0 , 3M9J , 3M9K , 3QFA , 3QFB , 3TRX , 4LL1 , 4LL4 , 4OO4 , 4OO5 , 4POK , 4POL , 4POM , 4PUF , 4TRX , 5DQY | ||||||||||
| Family and domains |
Pfam
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| Sequence |
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| Sequence length | 105 | ||||||||||
| Interactions | View interactions | ||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
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Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
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