SpliceAtlasDB
← 返回上一页

🧬 基因注释:TXNL4A

📝 官方信息

官方名称:thioredoxin like 4A

功能摘要: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].

🎯 作为靶基因的剪接因子
🏥 关联疾病
Choanal atresia-deafness-cardiac defects-dysmorphism syndrome
(0.764)
choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome
(0.747)
dengue disease
(0.370)
cleft palate
(0.370)
genetic disorder
(0.173)
🔍 查看该基因的所有关联疾病
🔗 外部数据库链接