LSM14B
Description
The LSM14B (LSM family member 14B) is a protein-coding gene located on chromosome 20.
LSM14B is also known as C20orf40, FAM61B, FT005, LSM13, RAP55B, bA11M20.3.
Associated Diseases
- female infertility due to oocyte meiotic arrest
- oocyte maturation defect 9
- premature ovarian failure 19
- hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
- hemoglobin D disease
- male infertility with teratozoospermia due to single gene mutation
- female infertility due to zona pellucida defect
- delta-beta-thalassemia
- dominant beta-thalassemia
- hemoglobin C-beta-thalassemia syndrome
- hemoglobin E-beta-thalassemia syndrome
- alpha-thalassemia-myelodysplastic syndrome
- hemoglobin E disease
- ring chromosome Y
