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Congenital anomalies of the kidney and urinary tract (CAKUT) v1.0 TFAP2A Gene migrated from ENSG00000137203 to ENSG00000137203 (gene set migration)
Congenital anomalies of the kidney and urinary tract (CAKUT) v0.63 TFAP2A Zornitza Stark Phenotypes for gene: TFAP2A were changed from Branchiooculofacial syndrome, MIM# 113620 to Branchiooculofacial syndrome, MIM# 113620
Congenital anomalies of the kidney and urinary tract (CAKUT) v0.62 TFAP2A Zornitza Stark Marked gene: TFAP2A as ready
Congenital anomalies of the kidney and urinary tract (CAKUT) v0.62 TFAP2A Zornitza Stark Gene: tfap2a has been classified as Green List (High Evidence).
Congenital anomalies of the kidney and urinary tract (CAKUT) v0.62 TFAP2A Zornitza Stark Phenotypes for gene: TFAP2A were changed from to Branchiooculofacial syndrome, MIM# 113620
Congenital anomalies of the kidney and urinary tract (CAKUT) v0.62 TFAP2A Zornitza Stark Mode of inheritance for gene: TFAP2A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Congenital anomalies of the kidney and urinary tract (CAKUT) v0.61 TFAP2A Zornitza Stark reviewed gene: TFAP2A: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Branchiooculofacial syndrome, MIM# 113620; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Congenital anomalies of the kidney and urinary tract (CAKUT) v0.0 TFAP2A Zornitza Stark gene: TFAP2A was added
gene: TFAP2A was added to Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: TFAP2A was set to Unknown