Mendeliome
Gene: PCK2 Amber List (moderate evidence)I don't know
A few more reported cases may clarify this possible gene-disease association.
PMID: 36845668 - three patients in two families with biallelic variants in PCK2 and supporting animal model. There are three p.(Ser23Ter) homozygotes reported in gnomAD, but given that the phenotype is not a severe paediatric phenotype and the homozygotes are not in the "healthy control" gnomAD cohorts it is plausible that these individuals could be affected.
DECIPHER Patient: 340038 - complex neurodevelpmental disorder phenotype, but does include sensory neuropathy with a stopgain and splice donor variant confirmed in trans
PMID: 32660061 - a heterozygous missense (Arg553Gln) identified in 2 pedigrees with 4 Shetland sheepdogs affected with paroxysmal exercise-induced dyskinesia.
There are also a couple of labs in ClinVar reporting LoF variants as likely pathogenic and pathogenic, but without any supporting evidence and/or information about the condition the variants are curated against.Created: 3 Mar 2023, 5:57 a.m. | Last Modified: 3 Mar 2023, 5:57 a.m.
Panel Version: 1.699
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Peripheral neuropathy (MONDO#0005244), PCK2-related
Publications
Red List (low evidence)
HGG journal
https://doi.org/10.1016/j.xhgg.2023.100182
2 families with 3 affected
1x chet missense + p.(Ser23Ter) which has 3 homs in gnomad v3_non_v2+v2)
1x hom NMD-predicted
all 3 patients have weakness and abnormal gait, abnormal conduction studies.
absence of PCK2 protein and profound reduction in activity in fibroblasts
KO mice displayed abnormal nerve conduction studies and peripheral nerve pathologyCreated: 2 Feb 2023, 3:40 a.m. | Last Modified: 2 Feb 2023, 3:40 a.m.
Panel Version: 1.632
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
peripheral neuropathy (MONDO#0005244), PCK2-related
Variants in this GENE are reported as part of current diagnostic practice
Red List (low evidence)
Note OMIM reported gene disease association with PEPCK deficiency, mitochondrial - MIM#261650
No published evidence identified supporting this.Created: 11 Apr 2022, 6:50 a.m. | Last Modified: 11 Apr 2022, 6:50 a.m.
Panel Version: 0.12855
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
PEPCK deficiency, mitochondrial - MIM#261650
Gene: pck2 has been classified as Amber List (Moderate Evidence).
Phenotypes for gene: PCK2 were changed from PEPCK deficiency, mitochondrial - MIM#261650 to PEPCK deficiency, mitochondrial - MIM#261650; peripheral neuropathy (MONDO#0005244), PCK2-related
Gene: pck2 has been classified as Red List (Low Evidence).
Phenotypes for gene: PCK2 were changed from to PEPCK deficiency, mitochondrial - MIM#261650
Mode of inheritance for gene: PCK2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Gene: pck2 has been classified as Red List (Low Evidence).
gene: PCK2 was added gene: PCK2 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: PCK2 was set to Unknown
If promoting or demoting a gene, please provide comments to justify a decision to move it.
Genes included in a Genomics England gene panel for a rare disease category (green list) should fit the criteria A-E outlined below.
These guidelines were developed as a combination of the ClinGen DEFINITIVE evidence for a causal role of the gene in the disease(a), and the Developmental Disorder Genotype-Phenotype (DDG2P) CONFIRMED DD Gene evidence level(b) (please see the original references provided below for full details). These help provide a guideline for expert reviewers when assessing whether a gene should be on the green or the red list of a panel.
A. There are plausible disease-causing mutations(i) within, affecting or encompassing an interpretable functional region(ii) of this gene identified in multiple (>3) unrelated cases/families with the phenotype(iii).
OR
B. There are plausible disease-causing mutations(i) within, affecting or encompassing cis-regulatory elements convincingly affecting the expression of a single gene identified in multiple (>3) unrelated cases/families with the phenotype(iii).
OR
C. As definitions A or B but in 2 or 3 unrelated cases/families with the phenotype, with the addition of convincing bioinformatic or functional evidence of causation e.g. known inborn error of metabolism with mutation in orthologous gene which is known to have the relevant deficient enzymatic activity in other species; existence of an animal model which recapitulates the human phenotype.
AND
D. Evidence indicates that disease-causing mutations follow a Mendelian pattern of causation appropriate for reporting in a diagnostic setting(iv).
AND
E. No convincing evidence exists or has emerged that contradicts the role of the gene in the specified phenotype.
(i)Plausible disease-causing mutations: Recurrent de novo mutations convincingly affecting gene function. Rare, fully-penetrant mutations - relevant genotype never, or very rarely, seen in controls. (ii) Interpretable functional region: ORF in protein coding genes miRNA stem or loop. (iii) Phenotype: the rare disease category, as described in the eligibility statement. (iv) Intermediate penetrance genes should not be included.
It’s assumed that loss-of-function variants in this gene can cause the disease/phenotype unless an exception to this rule is known. We would like to collect information regarding exceptions. An example exception is the PCSK9 gene, where loss-of-function variants are not relevant for a hypercholesterolemia phenotype as they are associated with increased LDL-cholesterol uptake via LDLR (PMID: 25911073).
If a curated set of known-pathogenic variants is available for this gene-phenotype, please contact us at panelapp@genomicsengland.co.uk
We classify loss-of-function variants as those with the following Sequence Ontology (SO) terms:
Term descriptions can be found on the PanelApp homepage and Ensembl.
If you are submitting this evaluation on behalf of a clinical laboratory please indicate whether you report variants in this gene as part of your current diagnostic practice by checking the box
Standardised terms were used to represent the gene-disease mode of inheritance, and were mapped to commonly used terms from the different sources. Below each of the terms is described, along with the equivalent commonly-used terms.
A variant on one allele of this gene can cause the disease, and imprinting has not been implicated.
A variant on the paternally-inherited allele of this gene can cause the disease, if the alternate allele is imprinted (function muted).
A variant on the maternally-inherited allele of this gene can cause the disease, if the alternate allele is imprinted (function muted).
A variant on one allele of this gene can cause the disease. This is the default used for autosomal dominant mode of inheritance where no knowledge of the imprinting status of the gene required to cause the disease is known. Mapped to the following commonly used terms from different sources: autosomal dominant, dominant, AD, DOMINANT.
A variant on both alleles of this gene is required to cause the disease. Mapped to the following commonly used terms from different sources: autosomal recessive, recessive, AR, RECESSIVE.
The disease can be caused by a variant on one or both alleles of this gene. Mapped to the following commonly used terms from different sources: autosomal recessive or autosomal dominant, recessive or dominant, AR/AD, AD/AR, DOMINANT/RECESSIVE, RECESSIVE/DOMINANT.
A variant on one allele of this gene can cause the disease, however a variant on both alleles of this gene can result in a more severe form of the disease/phenotype.
A variant in this gene can cause the disease in males as they have one X-chromosome allele, whereas a variant on both X-chromosome alleles is required to cause the disease in females. Mapped to the following commonly used term from different sources: X-linked recessive.
A variant in this gene can cause the disease in males as they have one X-chromosome allele. A variant on one allele of this gene may also cause the disease in females, though the disease/phenotype may be less severe and may have a later-onset than is seen in males. X-linked inactivation and mosaicism in different tissues complicate whether a female presents with the disease, and can change over their lifetime. This term is the default setting used for X-linked genes, where it is not known definitately whether females require a variant on each allele of this gene in order to be affected. Mapped to the following commonly used terms from different sources: X-linked dominant, x-linked, X-LINKED, X-linked.
The gene is in the mitochondrial genome and variants within this can cause this disease, maternally inherited. Mapped to the following commonly used term from different sources: Mitochondrial.
Mapped to the following commonly used terms from different sources: Unknown, NA, information not provided.
For example, if the mode of inheritance is digenic, please indicate this in the comments and which other gene is involved.