TM9SF2
Description
The TM9SF2 (transmembrane 9 superfamily member 2) is a protein-coding gene located on chromosome 13.
Transmembrane 9 superfamily member 2 is a protein produced from the TM9SF2 gene in humans.
This protein may function as a channel or small molecule transporter within intracellular compartments.
TM9SF2 is also known as Lnc-PCIR, P76.
Associated Diseases
- lysosomal storage disease
- asthma
- systemic lupus erythematosus
- type 1 diabetes mellitus
- hemoglobin D disease
- hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
- hemoglobin C-beta-thalassemia syndrome
- dominant beta-thalassemia
- hemoglobin H disease
- delta-beta-thalassemia
- hemoglobin E disease
- hemoglobin E-beta-thalassemia syndrome
- alpha-thalassemia-myelodysplastic syndrome
- hemolytic anemia due to diphosphoglycerate mutase deficiency
