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AP5Z1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

AP5Z1
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AP-5 complex subunit zeta (AP5Z1) is a protein that in humans is encoded by the AP5Z1 gene.[5]

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Function

The protein encoded by this gene is one of two large subunits of the AP5 adaptor complex. Damaging variants in this gene are associated with SPG48, a type of hereditary spastic paraplegia.[6][7]

References

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