TBC1D9B

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Description

The TBC1D9B (TBC1 domain family member 9B) is a protein-coding gene located on chromosome 5.

TBC1D9B is believed to act as a GTPase-activating protein (GAP) for members of the Rab family of proteins.

TBC1D9B is also known as GRAMD9B.

Associated Diseases

• hemoglobin E-beta-thalassemia syndrome
• hemoglobin D disease
• dehydrated hereditary stomatocytosis
• cholesterol-ester transfer protein deficiency
• hemolytic anemia due to erythrocyte adenosine deaminase overproduction
• sitosterolemia
• hypertriglyceridemia 2
• dominant beta-thalassemia
• hemoglobin E disease
• delta-beta-thalassemia
• IRIDA syndrome
• hemoglobin C-beta-thalassemia syndrome