| Gene Symbol | TXNL4A |
| Entrez Gene ID | 10907 |
| Full Name | thioredoxin like 4A |
| Synonyms | BMKS,DIB1,DIM1,SNRNP15,TXNL4,U5-15kD |
| General protein information |
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| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | The protein encoded by this gene is a member of the U5 small ribonucleoprotein particle (snRNP), and is involved in pre-mRNA splicing. This protein contains a thioredoxin-like fold and it is expected to interact with multiple proteins. Protein-protein interactions have been observed with the polyglutamine tract-binding protein 1 (PQBP1). Mutations in both the coding region and promoter region of this gene have been associated with Burn-McKeown syndrome, which is a rare disorder characterized by craniofacial dysmorphisms, cardiac defects, hearing loss, and bilateral choanal atresia. A pseudogene of this gene is found on chromosome 2. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2015]. |
| Disorder MIM: | |
| Disorder Html: | Burn-McKeown syndrome, 608572 (3) |
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