TXNL1
Description
The TXNL1 (thioredoxin like 1) is a protein-coding gene located on chromosome 18.
The TXNL1 gene in humans encodes the Thioredoxin-like protein 1.
TXNL1 is an active thioredoxin with a redox potential of approximately -250 mV.
TXNL1 is also known as HEL-S-114, TRP32, TXL-1, TXNL, Txl.
Associated Diseases
- schizophrenia
- primary familial polycythemia due to EPO receptor mutation
- alpha-thalassemia-myelodysplastic syndrome
- hemoglobin D disease
- hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
- beta-thalassemia-X-linked thrombocytopenia syndrome
- hemolytic anemia due to diphosphoglycerate mutase deficiency
- dehydrated hereditary stomatocytosis
- alpha thalassemia-intellectual disability syndrome type 1
- hemoglobin E-beta-thalassemia syndrome
- dominant beta-thalassemia
- hemoglobin E disease
- hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome
