IFT22

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Description

The IFT22 (intraflagellar transport 22) is a protein-coding gene located on chromosome 7.

IFT22 is a small GTPase-like protein that plays a crucial role in the intraflagellar transport (IFT) complex B.

IFT22 is also known as CFAP9, FAP9, RABL5.

Associated Diseases

• Jeune syndrome
• Alzheimer disease