Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
84817
Gene name Gene Name - the full gene name approved by the HGNC.
Thioredoxin domain containing 17
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TXNDC17
Synonyms (NCBI Gene) Gene synonyms aliases
TRP14, TXNL5
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17p13.1
miRNA miRNA information provided by mirtarbase database.
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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004601 Function Peroxidase activity IDA 14607844
GO:0005515 Function Protein binding IPI 14607844, 21044950, 25416956, 32296183
GO:0005829 Component Cytosol IBA 21873635
GO:0005829 Component Cytosol IDA 14607844
GO:0033209 Process Tumor necrosis factor-mediated signaling pathway IMP 14607844
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
616967 28218 ENSG00000129235
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Esophagus neoplasm Squamous cell carcinoma of esophagus rs28934578, rs121918714, rs1567556006, rs1575166666 21517111
Associations from Text Mining
Disease Name Relationship Type References
Neuroblastoma Associate 28498513
Ovarian Neoplasms Associate 25607466