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Congenital anomalies of the kidney and urinary tract (CAKUT) v1.0 CEP55 Gene migrated from ENSG00000138180 to ENSG00000138180 (gene set migration)
Congenital anomalies of the kidney and urinary tract (CAKUT) v0.28 CEP55 Zornitza Stark Marked gene: CEP55 as ready
Congenital anomalies of the kidney and urinary tract (CAKUT) v0.28 CEP55 Zornitza Stark Gene: cep55 has been classified as Green List (High Evidence).
Congenital anomalies of the kidney and urinary tract (CAKUT) v0.28 CEP55 Zornitza Stark Classified gene: CEP55 as Green List (high evidence)
Congenital anomalies of the kidney and urinary tract (CAKUT) v0.28 CEP55 Zornitza Stark Gene: cep55 has been classified as Green List (High Evidence).
Congenital anomalies of the kidney and urinary tract (CAKUT) v0.27 CEP55 Zornitza Stark Publications for gene: CEP55 were set to 28295209; 28264986
Congenital anomalies of the kidney and urinary tract (CAKUT) v0.27 CEP55 Zornitza Stark Classified gene: CEP55 as Green List (high evidence)
Congenital anomalies of the kidney and urinary tract (CAKUT) v0.27 CEP55 Zornitza Stark Gene: cep55 has been classified as Green List (High Evidence).
Congenital anomalies of the kidney and urinary tract (CAKUT) v0.26 CEP55 Zornitza Stark gene: CEP55 was added
gene: CEP55 was added to Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS. Sources: Expert Review
Mode of inheritance for gene: CEP55 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: CEP55 were set to 28295209; 28264986
Phenotypes for gene: CEP55 were set to Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly, MIM#236500
Review for gene: CEP55 was set to GREEN
Added comment: Two unrelated families and animal model.
Sources: Expert Review