EBNA1BP2

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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