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Growth failure v1.33 CENPJ Zornitza Stark Classified gene: CENPJ as Amber List (moderate evidence)
Growth failure v1.33 CENPJ Zornitza Stark Gene: cenpj has been classified as Amber List (Moderate Evidence).
Growth failure v1.32 CENPJ Zornitza Stark edited their review of gene: CENPJ: Added comment: PMID 34068194: two further families reported, same homozygous missense, founder?; Changed rating: AMBER; Changed publications: 20522431, 23166506, 34068194
Growth failure v0.195 CENPJ Zornitza Stark Marked gene: CENPJ as ready
Growth failure v0.195 CENPJ Zornitza Stark Gene: cenpj has been classified as Red List (Low Evidence).
Growth failure v0.195 CENPJ Zornitza Stark Phenotypes for gene: CENPJ were changed from seckel syndrome to Seckel syndrome 4, MIM# 613676
Growth failure v0.194 CENPJ Zornitza Stark Publications for gene: CENPJ were set to 20522431
Growth failure v0.193 CENPJ Zornitza Stark changed review comment from: Single family reported with Seckel phenotype and supportive mouse model. However, bi-allelic variants in this gene are typically associated with microcephaly.; to: Single family reported with Seckel phenotype and supportive mouse model. However, bi-allelic variants in this gene are typically associated with microcephaly without short stature.
Growth failure v0.193 CENPJ Zornitza Stark reviewed gene: CENPJ: Rating: RED; Mode of pathogenicity: None; Publications: 20522431, 23166506; Phenotypes: Seckel syndrome 4, MIM# 613676; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Growth failure v0.0 CENPJ Zornitza Stark gene: CENPJ was added
gene: CENPJ was added to Growth failure in early childhood. Sources: Genomics England PanelApp,Expert Review Red
Mode of inheritance for gene: CENPJ was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: CENPJ were set to 20522431
Phenotypes for gene: CENPJ were set to seckel syndrome