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Mitochondrial disease v0.1323 SLC19A3 Zornitza Stark Marked gene: SLC19A3 as ready
Mitochondrial disease v0.1323 SLC19A3 Zornitza Stark Gene: slc19a3 has been classified as Green List (High Evidence).
Mitochondrial disease v0.1323 SLC19A3 Zornitza Stark Phenotypes for gene: SLC19A3 were changed from to Thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2), MIM# 607483
Mitochondrial disease v0.1322 SLC19A3 Zornitza Stark Publications for gene: SLC19A3 were set to
Mitochondrial disease v0.1321 SLC19A3 Zornitza Stark Mode of inheritance for gene: SLC19A3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.0 SLC19A3 Zornitza Stark gene: SLC19A3 was added
gene: SLC19A3 was added to Mitochondrial_AGHA_VCGS. Sources: Expert Review Green,Australian Genomics Health Alliance Mitochondrial Flagship,Victorian Clinical Genetics Services
Mode of inheritance for gene: SLC19A3 was set to Unknown