EBNA1BP2
Description
The EBNA1BP2 (EBNA1 binding protein 2) is a protein-coding gene located on chromosome 1.
EBNA1BP2 is a protein involved in rRNA processing. It is encoded by the EBNA1BP2 gene in humans. EBNA1BP2 has been shown to interact with FGF3.
Plays a crucial role in the processing of the 27S pre-rRNA.
EBNA1BP2 is also known as EBP2, NOBP, P40.
Associated Diseases
- hemoglobin D disease
- dominant beta-thalassemia
- hemoglobin H disease
- hemoglobin C-beta-thalassemia syndrome
- hemoglobin E disease
- beta-thalassemia-X-linked thrombocytopenia syndrome
- hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
- hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome
- hemolytic anemia due to diphosphoglycerate mutase deficiency
- Mayer-Rokitansky-Kuster-Hauser syndrome
- overhydrated hereditary stomatocytosis
- erythroleukemia, familial, susceptibility to
- dehydrated hereditary stomatocytosis
- trimethylaminuria
- Senior-Boichis syndrome
