Gene Gene information from NCBI Gene database.
Entrez ID 84817
Gene name Thioredoxin domain containing 17
Gene symbol TXNDC17
Synonyms (NCBI Gene)
TRP14TXNL5
Chromosome 17
Chromosome location 17p13.1
miRNA miRNA information provided by mirtarbase database.
88
miRTarBase ID miRNA Experiments Reference
MIRT719816 hsa-miR-4328 HITS-CLIP 19536157
MIRT719815 hsa-miR-4729 HITS-CLIP 19536157
MIRT719814 hsa-miR-3143 HITS-CLIP 19536157
MIRT719813 hsa-miR-137 HITS-CLIP 19536157
MIRT719812 hsa-miR-5696 HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
11
GO ID Ontology Definition Evidence Reference
GO:0004601 Function Peroxidase activity IDA 14607844
GO:0005515 Function Protein binding IPI 14607844, 21044950, 25416956, 32296183
GO:0005737 Component Cytoplasm IEA
GO:0005829 Component Cytosol IBA
GO:0005829 Component Cytosol IDA 14607844
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616967 28218 ENSG00000129235
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9BRA2
Protein name Thioredoxin domain-containing protein 17 (14 kDa thioredoxin-related protein) (TRP14) (Protein 42-9-9) (Thioredoxin-like protein 5)
Protein function Disulfide reductase. May participate in various redox reactions through the reversible oxidation of its active center dithiol to a disulfide and catalyze dithiol-disulfide exchange reactions. Modulates TNF-alpha signaling and NF-kappa-B activati
PDB 1WOU
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF06110 DUF953 8 122 Eukaryotic protein of unknown function (DUF953) Family
Tissue specificity TISSUE SPECIFICITY: Ubiquitously expressed in cell lines. {ECO:0000269|PubMed:14607844}.
Sequence
Sequence length 123
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ESOPHAGEAL SQUAMOUS CELL CARCINOMA CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Carcinoma, Ovarian Epithelial Ovarian Epithelial carcinoma BEFREE 31524236
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of ovary Ovarian cancer BEFREE 31524236
★☆☆☆☆
Found in Text Mining only
Neuroblastoma Neuroblastoma BEFREE 28498513
★☆☆☆☆
Found in Text Mining only
Neuroblastoma Neuroblastoma Pubtator 28498513 Associate
★☆☆☆☆
Found in Text Mining only
ovarian neoplasm Ovarian neoplasm BEFREE 31524236
★☆☆☆☆
Found in Text Mining only
Ovarian Neoplasms Ovarian neoplasm Pubtator 25607466 Associate
★☆☆☆☆
Found in Text Mining only
Squamous cell carcinoma of esophagus Esophagus Neoplasm CTD_human_DG 21517111
★☆☆☆☆
Found in Text Mining only