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Mendeliome v1.4084 MIR17HG Zornitza Stark Classified gene: MIR17HG as Amber List (moderate evidence)
Mendeliome v1.4084 MIR17HG Zornitza Stark Gene: mir17hg has been classified as Amber List (Moderate Evidence).
Mendeliome v1.4083 MIR17HG Zornitza Stark changed review comment from: 4 unrelated cases reported - 3 with gene deletions, 1 with SNV
Sources: Expert list; to: 4 unrelated cases reported - 3 with gene deletions, 1 with SNV. The deletions include portion of GPC5 as well.
Sources: Expert list
Mendeliome v1.4083 MIR17HG Zornitza Stark edited their review of gene: MIR17HG: Changed rating: AMBER
Mendeliome v1.4083 MIR17HG Zornitza Stark Tag SV/CNV tag was added to gene: MIR17HG.
Mendeliome v1.4083 MIR17HG Zornitza Stark edited their review of gene: MIR17HG: Added comment: Multiple mouse models.; Changed publications: 25391829, 21892160, 29636449
Mendeliome v1.2374 MIR17HG Zornitza Stark Tag non-coding gene tag was added to gene: MIR17HG.
Mendeliome v0.168 MIR17HG Zornitza Stark Marked gene: MIR17HG as ready
Mendeliome v0.168 MIR17HG Zornitza Stark Gene: mir17hg has been classified as Green List (High Evidence).
Mendeliome v0.168 MIR17HG Zornitza Stark Classified gene: MIR17HG as Green List (high evidence)
Mendeliome v0.168 MIR17HG Zornitza Stark Gene: mir17hg has been classified as Green List (High Evidence).
Mendeliome v0.167 MIR17HG Zornitza Stark gene: MIR17HG was added
gene: MIR17HG was added to Mendeliome_VCGS. Sources: Expert list
Mode of inheritance for gene: MIR17HG was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: MIR17HG were set to 25391829; 21892160
Phenotypes for gene: MIR17HG were set to Feingold syndrome 2; OMIM #614326
Review for gene: MIR17HG was set to GREEN
Added comment: 4 unrelated cases reported - 3 with gene deletions, 1 with SNV
Sources: Expert list