R3HCC1L

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Description

The R3HCC1L (R3H domain and coiled-coil containing 1 like) is a protein-coding gene located on chromosome 10.

R3HCC1L is also known as C10orf28, GIDRP86, GIDRP88, PSORT.

Associated Diseases

• hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
• hemoglobin D disease
• alpha thalassemia-intellectual disability syndrome type 1
• delta-beta-thalassemia
• hemoglobin E-beta-thalassemia syndrome
• dominant beta-thalassemia
• hemoglobin C-beta-thalassemia syndrome
• alpha-thalassemia-myelodysplastic syndrome
• Heinz body anemia
• hemoglobin E disease
• hemoglobin H disease