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Fetal anomalies v1.184 CELSR1 Chern Lim edited their review of gene: CELSR1: Changed rating: GREEN
Fetal anomalies v1.184 CELSR1 Ain Roesley Publications for gene: CELSR1 were set to 31215153; 31403174; 26855770
Fetal anomalies v1.183 CELSR1 Ain Roesley Classified gene: CELSR1 as Green List (high evidence)
Fetal anomalies v1.183 CELSR1 Ain Roesley Gene: celsr1 has been classified as Green List (High Evidence).
Fetal anomalies v1.182 CELSR1 Chern Lim reviewed gene: CELSR1: Rating: AMBER; Mode of pathogenicity: None; Publications: 38272662; Phenotypes: hydrops fetalis (MONDO:0015193), CELSR1-related; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Fetal anomalies v0.1193 CELSR1 Zornitza Stark Marked gene: CELSR1 as ready
Fetal anomalies v0.1193 CELSR1 Zornitza Stark Gene: celsr1 has been classified as Red List (Low Evidence).
Fetal anomalies v0.1193 CELSR1 Zornitza Stark Phenotypes for gene: CELSR1 were changed from Lymphatic malformation 9, OMIM:619319 to Lymphatic malformation 9, MIM# 619319
Fetal anomalies v0.1192 CELSR1 Zornitza Stark Publications for gene: CELSR1 were set to
Fetal anomalies v0.1191 CELSR1 Zornitza Stark Mode of inheritance for gene: CELSR1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Fetal anomalies v0.1190 CELSR1 Zornitza Stark Classified gene: CELSR1 as Red List (low evidence)
Fetal anomalies v0.1190 CELSR1 Zornitza Stark Gene: celsr1 has been classified as Red List (Low Evidence).
Fetal anomalies v0.1189 CELSR1 Zornitza Stark reviewed gene: CELSR1: Rating: RED; Mode of pathogenicity: None; Publications: 31215153, 31403174, 26855770; Phenotypes: Lymphatic malformation 9, MIM# 619319; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Fetal anomalies v0.0 CELSR1 Zornitza Stark gene: CELSR1 was added
gene: CELSR1 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp
Mode of inheritance for gene: CELSR1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: CELSR1 were set to Lymphatic malformation 9, OMIM:619319