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Brain Calcification v3.0 ACP5 Gene migrated from ENSG00000102575 to ENSG00000102575 (gene set migration)
Brain Calcification v1.23 ACP5 Zornitza Stark Phenotypes for gene: ACP5 were changed from Spondyloenchondrodysplasia with immune dysregulation, MIM# 607944 to Spondyloenchondrodysplasia with immune dysregulation, MIM# 607944
Brain Calcification v1.23 ACP5 Zornitza Stark Phenotypes for gene: ACP5 were changed from Spondyloenchondrodysplasia, short stature, SLE, intracranial calcification, spasticity, chilblains, autoimmune haemolytic anaemia to Spondyloenchondrodysplasia with immune dysregulation, MIM# 607944
Brain Calcification v1.22 ACP5 Zornitza Stark edited their review of gene: ACP5: Changed phenotypes: Spondyloenchondrodysplasia with immune dysregulation, MIM# 607944
Brain Calcification v1.22 ACP5 Yetong Chen changed review comment from: PMID 21217755 reports 4 unrelated individuals with ACP5 variants who developed intracranial calcification.
PMID 21217752 reports 4 individuals with ACP5 variants who developed brain calcification.; to: PMID 21217755 reports 4 unrelated individuals with ACP5 variants who developed intracranial calcification.
PMID 21217752 reports 4 individuals with ACP5 variants who developed brain calcification.
Brain Calcification v1.22 ACP5 Yetong Chen reviewed gene: ACP5: Rating: GREEN; Mode of pathogenicity: None; Publications: 24372060, 21217755; Phenotypes: Spondyloenchondrodysplasia with immune dysregulation, SPENCDI; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Brain Calcification v0.20 ACP5 Zornitza Stark Marked gene: ACP5 as ready
Brain Calcification v0.20 ACP5 Zornitza Stark Gene: acp5 has been classified as Green List (High Evidence).
Brain Calcification v0.20 ACP5 Zornitza Stark Classified gene: ACP5 as Green List (high evidence)
Brain Calcification v0.20 ACP5 Zornitza Stark Gene: acp5 has been classified as Green List (High Evidence).
Brain Calcification v0.19 ACP5 Zornitza Stark gene: ACP5 was added
gene: ACP5 was added to Brain Calcification. Sources: Expert list
Mode of inheritance for gene: ACP5 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ACP5 were set to 21217755; 21217752
Phenotypes for gene: ACP5 were set to Spondyloenchondrodysplasia, short stature, SLE, intracranial calcification, spasticity, chilblains, autoimmune haemolytic anaemia
Review for gene: ACP5 was set to GREEN
Added comment: Established gene-disease association, intracranial calcification is part of the phenotype.
Sources: Expert list