Identity
HGNC
LOCATION
5q31.1
LOCUSID
ALIAS
BUG,C5orf14,UNQ335
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 79770
MIM: 617778
HGNC: 20652
Ensembl: ENSG00000113621
Variants:
dbSNP: 79770
ClinVar: 79770
TCGA: ENSG00000113621
COSMIC: TXNDC15
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 30851085 | 2019 | A prenatally diagnosed case of Meckel-Gruber syndrome with novel compound heterozygous pathogenic variants in the TXNDC15 gene. | 5 |
| 30851085 | 2019 | A prenatally diagnosed case of Meckel-Gruber syndrome with novel compound heterozygous pathogenic variants in the TXNDC15 gene. | 5 |
| 21642008 | 2011 | Cell surface thiol isomerases may explain the platelet-selective action of S-nitrosoglutathione. | 5 |
| 21642008 | 2011 | Cell surface thiol isomerases may explain the platelet-selective action of S-nitrosoglutathione. | 5 |
Citation
Dessen P
TXNDC15 (thioredoxin domain containing 15)
Atlas Genet Cytogenet Oncol Haematol. 2014-08-01
Online version: http://atlasgeneticsoncology.org/gene/54742/submit-meetings/teaching-explorer/
