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Amelogenesis imperfecta v2.18 PEX6 Sarah Leigh edited their review of gene: PEX6: Added comment: For Peroxisome biogenesis disorder 4B (OMIM:614863), Falkenberg et al (PMID: 29220678) has identified Allelic Expression Imbalance (AEI) as a mechanism responsible for the condition. Affected patients (7 unrelated cases) were monoallelic for rs61753230 (c.2578C>T, p.Arg860Trp) and rs144286892 (c.∗442_445 delTAAA), with these variants being on the same chromosome (cis). It would appear that rs144286892 causes the over expression of the allele that it is on, resulting in over expression of rs61753230. The unaffected parents analysed were monoallelic for rs61753230 and biallelic for rs144286892, resulting in overexpression of both rs61753230 and wild type alleles (PMID: 29220678). Experimental evidence revealed that rs61753230 has a dominant-negative effect on the function of the PEX1- PEX6 complex in peroxisomal matrix protein import (PMID: 29220678).; Changed mode of pathogenicity: Other; Changed publications to: 29220678
Amelogenesis imperfecta PEX1 Rebecca Foulger marked PEX1 as ready
Amelogenesis imperfecta PEX1 Claire Smith reviewed PEX1
Amelogenesis imperfecta PEX1 Rebecca Foulger classified PEX1 as green
Amelogenesis imperfecta PEX1 Rebecca Foulger commented on PEX1
Amelogenesis imperfecta PEX1 Rebecca Foulger commented on PEX1
Amelogenesis imperfecta PEX1 Rebecca Foulger commented on PEX1