Gene Validity Curation

Gene Validity Classification Summary

Gene/Disease Pair:

PKD2 : autosomal dominant polycystic kidney disease

HGNC:9009 | MONDO_0004691
Mode of Inheritance: Autosomal dominant inheritance (HP:0000006)
Expert Panel: Harvard/Geisinger Biocuration Core
SOP: Gene Clinical Validity Standard Operating Procedures (SOP), Version 5

Genetic Evidence
Case-Level Data
Evidence Type Case Information Type Guidelines Points PMIDs/Notes
Default Range Max Total Counted
Variant Evidence
Autosomal Dominant or X-linked Disorder Variant is de novo 2 0-3 12
Proband with predicted or proven null variant 1.5 0-2 10 15 10
Mochizuki T et al. 1996 May 31 (PMID:8650545); Pei Y et al. 1998 May (PMID:9573526); Torra R et al. 1999 Jul (PMID:10411676);
Proband with other variant type with some evidence of gene impact 0.5 0-1.5 7
0.6
0.6
Torra R et al. 1999 Jul (PMID:10411676); Veldhuisen B et al. 1997 Sep (PMID:9326320); Xu D et al. 2018 Mar 6 (PMID:29529603); Chang MY et al. 2013 Nov (PMID:23985799);
Autosomal Recessive Disease Two variants in trans and at least one de novo or a predicted/proven null variant 2 0-3 12
Two variants (not predicted/proven null) with some evidence of gene impact in trans 1 0-1.5
Segregation Evidence Evidence of segregation in one or more families   Sequencing Method 0-3 3
3
3  
Total LOD Score Canditate Gene Sequencing Exome/Genome or all genes sequenced in linkage region  
2-2.99 0.5 1
Mochizuki T et al. 1996 May 31 (PMID:8650545);
3-4.99 1 2
Pei Y et al. 1998 May (PMID:9573526);
≥5 1.5 3
Case-Control Data
Case-Control Study Type Case-Control Quality Criteria Guidelines Points PMIDs/Notes
Points/Study Max Total Counted
Single Variant Analysis 1. Variant Detection Methodology
2. Power
3. Bias and confounding
4. Statistical Significance
0-6 12
Aggregate Variant Analysis 0-6
Total Genetic Evidence Points (Maximum 12) 12
Experimental Evidence
Evidence Category Evidence Type Guidelines Points PMIDs/Notes
Default Range Max Total Counted
Function Biochemical Function 0.5 0 - 2 2
Protein Interaction 0.5 0 - 2
Expression 0.5 0 - 2
Functional Alteration Patient cells 1 0 - 2 2
Non-patient cells 0.5 0 - 1
Models Non-human model organism 2 0 - 4 4 2 4
Wu G et al. 1998 Apr 17 (PMID:9568711);
Cell culture model 1 0 - 2
Rescue Rescue in human 2 0 - 4
Rescue in non-human model organism 2 0 - 4
2
Li A et al. 2015 Oct (PMID:26435415);
Rescue in cell culture model 1 0 - 2
Rescue in patient cells 1 0 - 2
Total Experimental Evidence Points (Maximum 6) 4

 


 

Assertion criteria Genetic Evidence (0-12 points) Experimental Evidence
(0-6 points)
Total Points
(0-18)
Replication Over Time (Y/N)
Description Case-level, family segregation, or case-control data that support the gene-disease association Gene-level experimental evidence that support the gene-disease association Sum of Genetic & Experimental
Evidence
> 2 pubs w/ convincing evidence over time (>3 yrs)
Assigned Points 12 4 16 YES
CALCULATED CLASSIFICATION LIMITED 1-6
MODERATE 7-11
STRONG 12-18
DEFINITIVE 12-18 AND replication over time
Valid contradictory evidence (Y/N)*
NO
CALCULATED CLASSIFICATION (DATE)
Definitive
06/25/2018
EXPERT CURATION (DATE)
Definitive
09/11/2018
EVIDENCE SUMMARY
The PKD2 gene has been associated with autosomal dominant polycystic kidney disease in over 15 probands in 6 curated publications. PKD2 was first associated with this disease in humans in 1996 (Mochizuki et al.). Variants in this gene segregate with disease and can occur de novo. The mechanism for disease is known to be loss of function. 53 unique variants (missense, in-frame indel, nonsense, frameshift, large deletion and complex rearrangements) have been classified as Pathogenic in ClinVar, 30 of which are frameshift, nonsense or consensus splice changes. More evidence is available in the literature, but the maximum score for genetic evidence (12 pts.) has been reached. This gene-disease association is supported by animal models that recapitulate the human disease. In summary, PKD2 is definitively associated with autosomal dominant polycystic kidney disease. This has been repeatedly demonstrated in both the research and clinical diagnostic settings, and has been upheld over time.