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Parkinson Disease and Complex Parkinsonism v1.108 C19orf12 Sarah Leigh Added comment: Comment on mode of inheritance: Monfrini et al (PMID: 29295770) and Gregory et al (PMID: 31087512) have reported heterozygous pathogenic C19ORF12 variants in patients with neurodegeneration with brain iron accumulation 4 (OMIM: 614298). Therefore, the mode of inheritance for this gene should be BOTH monoallelic and biallelic, autosomal or pseudoautosomal.
Parkinson Disease and Complex Parkinsonism v1.108 C19orf12 Sarah Leigh Mode of inheritance for gene: C19orf12 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Parkinson Disease and Complex Parkinsonism v1.107 C19orf12 Sarah Leigh Phenotypes for gene: C19orf12 were changed from Dystonia; mitochondrial membrane protein-associated neurodegeneration; Neurodegeneration with brain iron accumulation 4 to ?Spastic paraplegia 43, autosomal recessive, OMIM:615043; Neurodegeneration with brain iron accumulation 4, OMIM: 614298
Parkinson Disease and Complex Parkinsonism v1.106 C19orf12 Sarah Leigh Publications for gene: C19orf12 were set to
Parkinson Disease and Complex Parkinsonism C19orf12 Arianna Tucci reviewed C19orf12
Parkinson Disease and Complex Parkinsonism C19orf12 Ellen McDonagh marked C19orf12 as ready
Parkinson Disease and Complex Parkinsonism C19orf12 Ellen McDonagh classified C19orf12 as green
Parkinson Disease and Complex Parkinsonism C19orf12 Ellen McDonagh classified C19orf12 as green