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Fetal anomalies v0.546 DSTYK Zornitza Stark Marked gene: DSTYK as ready
Fetal anomalies v0.546 DSTYK Zornitza Stark Gene: dstyk has been classified as Red List (Low Evidence).
Fetal anomalies v0.546 DSTYK Zornitza Stark Phenotypes for gene: DSTYK were changed from CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT, CAKUT1 to Congenital anomalies of kidney and urinary tract 1, MIM# 610805; Spastic paraplegia 23, MIM# 270750
Fetal anomalies v0.545 DSTYK Zornitza Stark Publications for gene: DSTYK were set to
Fetal anomalies v0.544 DSTYK Zornitza Stark Mode of inheritance for gene: DSTYK was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Fetal anomalies v0.543 DSTYK Zornitza Stark Classified gene: DSTYK as Red List (low evidence)
Fetal anomalies v0.543 DSTYK Zornitza Stark Gene: dstyk has been classified as Red List (Low Evidence).
Fetal anomalies v0.542 DSTYK Zornitza Stark reviewed gene: DSTYK: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Fetal anomalies v0.535 DSTYK Belinda Chong reviewed gene: DSTYK: Rating: AMBER; Mode of pathogenicity: None; Publications: 28157540,23862974; Phenotypes: Spastic paraplegia 23, MIM# 270750; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Fetal anomalies v0.0 DSTYK Zornitza Stark gene: DSTYK was added
gene: DSTYK was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp
Mode of inheritance for gene: DSTYK was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: DSTYK were set to CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT, CAKUT1