AAAS : aladin WD repeat nucleoporin

Unlocking the Enigma of the ALADIN Protein: A Journey into Molecular Biology


The ALADIN gene, located on chromosome 12q13.13, holds the blueprint for creating a protein of the same name. ALADIN resides within the nuclear envelope, the gateway between the nucleus and the cytoplasm, suggesting its involvement in the intricate dance of molecular transport. While its precise function remains shrouded in mystery, ALADIN‘s presence in this vital cellular structure hints at its significance in regulating the flow of information and materials between the nucleus and the rest of the cell.

Associated Diseases

Mutations in the ALADIN gene have been linked to a rare genetic disorder called neurodegeneration with brain iron accumulation. This devastating condition manifests with a constellation of symptoms, including movement difficulties, cognitive impairment, and premature death. The accumulation of iron in the brain is a hallmark of the disease, suggesting iron dysregulation as a potential underlying mechanism.

Did you Know ?

The prevalence of neurodegeneration with brain iron accumulation is estimated to be around 1:100,000, highlighting its rarity. However, its rarity underscores the importance of deciphering the role of ALADIN, as its insights may shed light on other neurodegenerative disorders.

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