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Cholestasis v1.45 NPHP3 Ivone Leong Classified gene: NPHP3 as Amber List (moderate evidence)
Cholestasis v1.45 NPHP3 Ivone Leong Added comment: Comment on list classification: New gene added by Zornitza Stark. There is enough evidence to support a gene-disease association; however, as cholestasis is not a prominant feature of Renal-hepatic-pancreatic dysplasia and there does not appear to be any cases with isolated cholestasis phenotype. Therefore, this gene has been given an Amber rating.

This gene is Green on Cystic kidney disease (v2.19), Unexplained paediatric onset end-stage renal disease (v1.11), Fetal anomalies (v1.92) and Renal ciliopathies (v1.30).

It is also Amber on Neonatal cholestasis (v1.4) with the following review:
"Comment on list classification: Cholestasis is not a major feature of Nephronophthisis 3. Biallelic variants in this gene have been reported in Caroli syndrome and renal-hepatic-pancreatic dysplasia; only a small number of cases have been reported and features vary. It would be less likely for variants in this gene to present with isolated cholestasis; NPHP3 is on a number of other panels including rare multisystem ciliopathies and cystic kidneys.
Anna de Burca (Genomics England Curator), 25 Jul 2018"
Cholestasis v1.45 NPHP3 Ivone Leong Gene: nphp3 has been classified as Amber List (Moderate Evidence).
Cholestasis v1.44 NPHP3 Ivone Leong Publications for gene: NPHP3 were set to 18371931; 20007846; 32341812
Cholestasis v1.37 NPHP3 Ivone Leong Phenotypes for gene: NPHP3 were changed from Renal-hepatic-pancreatic dysplasia 1, MIM# 208540 to Renal-hepatic-pancreatic dysplasia 1, 208540
Cholestasis v1.16 NPHP3 Zornitza Stark gene: NPHP3 was added
gene: NPHP3 was added to Cholestasis. Sources: Expert list
Mode of inheritance for gene: NPHP3 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NPHP3 were set to 18371931; 20007846; 32341812
Phenotypes for gene: NPHP3 were set to Renal-hepatic-pancreatic dysplasia 1, MIM# 208540
Review for gene: NPHP3 was set to GREEN
Added comment: Very rare ciliopathy with prominent liver phenotype, including cholestasis.
Sources: Expert list