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Intellectual disability - microarray and sequencing v3.1374 PRDM12 Sarah Leigh Mode of inheritance for gene: PRDM12 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability - microarray and sequencing v3.1373 PRDM12 Sarah Leigh Phenotypes for gene: PRDM12 were changed from NA to Neuropathy, hereditary sensory and autonomic, type VIII OMIM:616488; congenital insensitivity to pain-hypohidrosis syndrome MONDO:0014662
Intellectual disability - microarray and sequencing v3.1372 PRDM12 Sarah Leigh Publications for gene: PRDM12 were set to
Intellectual disability - microarray and sequencing v3.624 PRDM12 Arina Puzriakova Classified gene: PRDM12 as Red List (low evidence)
Intellectual disability - microarray and sequencing v3.624 PRDM12 Arina Puzriakova Added comment: Comment on list classification: Following discussion with the Genomics England clinical team, this gene has been demoted from Amber to Red, in accordance with the external review by Zornitza Stark (Australian Genomics)
Intellectual disability - microarray and sequencing v3.624 PRDM12 Arina Puzriakova Gene: prdm12 has been classified as Red List (Low Evidence).
Intellectual disability - microarray and sequencing v3.3 PRDM12 Zornitza Stark reviewed gene: PRDM12: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Neuropathy, hereditary sensory and autonomic, type VIII, MIM# 616488; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability - microarray and sequencing PRDM12 BRIDGE consortium edited their review of PRDM12
Intellectual disability - microarray and sequencing PRDM12 Louise Daugherty classified PRDM12 as amber
Intellectual disability - microarray and sequencing PRDM12 Louise Daugherty commented on PRDM12
Intellectual disability - microarray and sequencing PRDM12 BRIDGE consortium reviewed PRDM12