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Date	Panel	Item	Activity
Filter activities 9 actions
14 Dec 2021	Fetal anomalies v0.1346	CLMP	Zornitza Stark Marked gene: CLMP as ready
14 Dec 2021	Fetal anomalies v0.1346	CLMP	Zornitza Stark Gene: clmp has been classified as Green List (High Evidence).
14 Dec 2021	Fetal anomalies v0.1346	CLMP	Zornitza Stark Phenotypes for gene: CLMP were changed from CONGENITAL SHORT BOWEL SYNDROME to Congenital short bowel syndrome , MIM#615237
14 Dec 2021	Fetal anomalies v0.1345	CLMP	Zornitza Stark Publications for gene: CLMP were set to
14 Dec 2021	Fetal anomalies v0.1344	CLMP	Zornitza Stark Classified gene: CLMP as Green List (high evidence)
14 Dec 2021	Fetal anomalies v0.1344	CLMP	Zornitza Stark Gene: clmp has been classified as Green List (High Evidence).
14 Dec 2021	Fetal anomalies v0.1343	CLMP	Zornitza Stark changed review comment from: Well established gene-disease association.; to: Well established gene-disease association, malrotation is a feature.
14 Dec 2021	Fetal anomalies v0.1343	CLMP	Zornitza Stark reviewed gene: CLMP: Rating: GREEN; Mode of pathogenicity: None; Publications: 22155368; Phenotypes: Congenital short bowel syndrome , MIM#615237; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
24 Oct 2021	Fetal anomalies v0.0	CLMP	Zornitza Stark gene: CLMP was added gene: CLMP was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp Mode of inheritance for gene: CLMP was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: CLMP were set to CONGENITAL SHORT BOWEL SYNDROME