<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(3)</volume><submitter>Riffe RM</submitter><funding>University of Massachusetts Amherst</funding><pubmed_abstract>The five-subunit endosomal Rab5 and RNA/ribose intermediary (FERRY) complex is a newly described protein complex consisting of TBCK, PPP1R21, FERRY3 (previously C12orf4), CRYZL1, and GATD1. The FERRY complex is proposed to function as a Rab5 effector to shuttle mRNA to the cell periphery for local translation, a process especially important in cells with far reaching processes. Interestingly, three members of the FERRY complex are associated with ultra-rare neurogenetic disorders. Mutation of TBCK causes TBCK syndrome, mutation of PPP1R21 is associated with PPP1R21-related intellectual disability, and mutation of FERRY3 results in an autosomal recessive intellectual disability. Neurologic disorders have yet to be associated with mutation of GATD1 or CRYZL1. Here, we provide a review of eac</pubmed_abstract><journal>Biology open</journal><pagination>BIO061808</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11928052</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Neurogenetic disorders associated with mutations in the FERRY complex: a novel disease class?</pubmed_title><pmcid>PMC11928052</pmcid><pubmed_authors>Riffe RM</pubmed_authors><pubmed_authors>Downes GB</pubmed_authors></additional><is_claimable>false</is_claimable><name>Neurogenetic disorders associated with mutations in the FERRY complex: a novel disease class?</name><description>The five-subunit endosomal Rab5 and RNA/ribose intermediary (FERRY) complex is a newly described protein complex consisting of TBCK, PPP1R21, FERRY3 (previously C12orf4), CRYZL1, and GATD1. The FERRY complex is proposed to function as a Rab5 effector to shuttle mRNA to the cell periphery for local translation, a process especially important in cells with far reaching processes. Interestingly, three members of the FERRY complex are associated with ultra-rare neurogenetic disorders. Mutation of TBCK causes TBCK syndrome, mutation of PPP1R21 is associated with PPP1R21-related intellectual disability, and mutation of FERRY3 results in an autosomal recessive intellectual disability. Neurologic disorders have yet to be associated with mutation of GATD1 or CRYZL1. Here, we provide a review of eac</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2026-04-08T19:51:35.838Z</modification><creation>2026-04-08T14:31:02.086Z</creation></dates><accession>S-EPMC11928052</accession><cross_references><pubmed>40062705</pubmed><doi>10.1242/bio.061808</doi></cross_references></HashMap>