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Heterotaxy v0.89 CRELD1 Zornitza Stark Classified gene: CRELD1 as Amber List (moderate evidence)
Heterotaxy v0.89 CRELD1 Zornitza Stark Gene: creld1 has been classified as Amber List (Moderate Evidence).
Heterotaxy v0.88 CRELD1 Zornitza Stark changed review comment from: Three families reported with heterozygous missense variants and heterotaxy phenotype.
Sources: Expert list; to: Three families reported with heterozygous missense variants and heterotaxy phenotype. However, supporting evidence of pathogenicity for some of the variants is relatively weak.
Sources: Expert list
Heterotaxy v0.88 CRELD1 Zornitza Stark edited their review of gene: CRELD1: Changed rating: AMBER
Heterotaxy v0.29 CRELD1 Zornitza Stark Marked gene: CRELD1 as ready
Heterotaxy v0.29 CRELD1 Zornitza Stark Gene: creld1 has been classified as Green List (High Evidence).
Heterotaxy v0.29 CRELD1 Zornitza Stark Classified gene: CRELD1 as Green List (high evidence)
Heterotaxy v0.29 CRELD1 Zornitza Stark Gene: creld1 has been classified as Green List (High Evidence).
Heterotaxy v0.28 CRELD1 Zornitza Stark gene: CRELD1 was added
gene: CRELD1 was added to Heterotaxy. Sources: Expert list
Mode of inheritance for gene: CRELD1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: CRELD1 were set to 22740159
Phenotypes for gene: CRELD1 were set to Atrioventricular septal defect, partial, with heterotaxy syndrome 606217
Review for gene: CRELD1 was set to GREEN
Added comment: Three families reported with heterozygous missense variants and heterotaxy phenotype.
Sources: Expert list