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Likely inborn error of metabolism - targeted testing not possible v1.188 MTPAP Sarah Leigh Added comment: Comment on phenotypes: Required for mitochondrial gene expression (Mitochondrial respiratory chain disorders (caused by nuclear variants only)
Likely inborn error of metabolism - targeted testing not possible v1.188 MTPAP Sarah Leigh Phenotypes for gene: MTPAP were changed from ?Spastic ataxia 4, autosomal recessive 613672; Ataxia, spastic, 4, 613672; ?Spastic ataxia 4, autosomal recessive, 613672; Required for mitochondrial gene expression (Mitochondrial respiratory chain disorders (caused by nuclear variants only) to ?Spastic ataxia 4, autosomal recessive 613672
Likely inborn error of metabolism - targeted testing not possible v1.76 MTPAP Sarah Leigh Source Expert Review Green was added to MTPAP.
Added phenotypes ?Spastic ataxia 4, autosomal recessive 613672 for gene: MTPAP
Publications for gene MTPAP were changed from 27604308 to 27959697; 26319014; 25008111; 20970105; 27391121
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Likely inborn error of metabolism - targeted testing not possible v1.47 MTPAP Ivone Leong Source NHS GMS was added to MTPAP.
Source London North GLH was added to MTPAP.
Likely inborn error of metabolism - targeted testing not possible v0.4 MTPAP Ellen McDonagh Added phenotypes Ataxia, spastic, 4, 613672 for gene: MTPAP
Likely inborn error of metabolism - targeted testing not possible v0.4 MTPAP Ellen McDonagh gene: MTPAP was added
gene: MTPAP was added to Inborn errors of metabolism. Sources: Expert Review Amber
Mode of inheritance for gene: MTPAP was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: MTPAP were set to 27604308
Phenotypes for gene: MTPAP were set to ?Spastic ataxia 4, autosomal recessive, 613672; Required for mitochondrial gene expression (Mitochondrial respiratory chain disorders (caused by nuclear variants only)