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Gene-disease assertions not curated here (add link or write note):

Disease

hereditary pheochromocytoma-paraganglioma

Inheritance

Autosomal dominant (with paternal transmission effect)

Prevalence

 1-9 / 1 000 000

Source: ORPHA:29072

Rapid or full curation?

  • Rapid
  • Full

ClinGen / GenCC / BabySeq / HGMD

Hereditary Cancer GCEP, accessed 06.30.2023

Clinical Validity Scoring Notes and points

Hereditary Paraganglioma-Pheochromocytoma Syndromes (PGL/PCC) [MONDO:0017366, PMID: 20301715] are associated with an increased risk of multiple paragangliomas and pheochromocytomas tumors within multiple organ systems transmitted in autosomal dominant inheritance. The molecular mechanism is loss of function in one of the 4 genes comprising the succinate dehydrogenase and SDHAF gene for flavination of SDHA, and stabilization of the SDH complex. This is a curation for SDHAF2 and SDHAF2 associated Hereditary Paraganglioma-Pheochromocytoma syndromes (PGL/PCC) (Paraganglioma 2, MIM: 601650). SDHAF2 was first reported in relation to PGL/PCC in 2009 [Hao et al., PMID: 19628817]. SDHAF2 related hereditary PGL/PCC syndromes are rare and only account for less than 0.1% of the cases with PGL/PCC. A Dutch founder variant in exon 2 of SDHAF2 gene, NM_017841.2(SDHAF2):c.232G>A (p.Gly78Arg), was identified in a large Dutch family via linkage study over a 30 years of period, which showed a parent-of-origin effect [PMIDs: 19628817, 6286462, 7814027, 8388849, 21224366]. Evidence suggests that this pathogenic variant in exon 2 of SDHAF2 destabilizes the protein, impairing its interaction with SDHA [PMID: 19628817]. This variant was also reported in a small Spanish family [PMID: 20071235], and sporadic cases [PMID: 28384794]. A variant at the same codon, but with different nucleotide change, NM_017841.4:c.232G>C p.Gly78Arg, was reported in a sporadic case from a cohort of 79 patients [PMID: 22241717]. Another missense variant and three nonsense variants are included in this curation [PMIDs: 26096992, 26269449, 22241717]. More evidence is available in the literature, but the maximum score for genetic evidence (12 pts.) has been reached. Experimental evidence is mainly from a comprehensive study on the p.Gly78Arg Dutch founder variant [PMID: 19628817]. The SDHA flavination was decreased which results from impaired interaction with SDHA in patients’ tumor cells. In yeast model, wt hSDHAF2 can rescue growth defects by increasing the falvination in the model with yeast sdh5 deletion, but this missense variant had no such rescuing effect. Other studies in yeast also indicated mutations in yeast sdh5 disrupt the covalent flavination of sdh1 [PMID: 23062074]. In summary, SDHAF2 gene is definitely associated with autosomal dominant HPGL/PCC syndrome. This has been repeatedly demonstrated in both the research and clinical diagnostic settings and has been upheld over time.

Source: Hereditary Cancer GCEP, accessed 06.30.2023

Clinical Validity Points Total

18

Source: Hereditary Cancer GCEP, accessed 06.30.2023

Clinical Validity Classification

 Classifications (pts)

Definitive (12pts)

Strong (12pts)

Moderate (7-11pts)

Limited (0.1-6pts)

No genetic evidence

Refuted

Disputed

Definitive

Source: Hereditary Cancer GCEP, accessed 06.30.2023

Molecular Mechanism

 Mechanisms

Loss of function

Gain of function

Dominant negative

Unknown

Other

Loss of function

Source: Hereditary Cancer GCEP, accessed 06.30.2023

Penetrance

 options

Complete (100%)

High (≥90%)

Reduced  (<90% and >10%)

Low (≤10%)

(list source/PMID)

Unknown, but age related and parent of origin effect with higher risk from paternally inherited alleles.

Source:https://actionability.clinicalgenome.org/ac/Adult/ui/stg2SummaryRpt?doc=AC150 , PMID: 26067997, 19628817.

Age of Onset

 options

Congenital

Pediatric

Adolescent

Adulthood

Late adulthood

(list source/PMID)

Adulthood

Source: https://actionability.clinicalgenome.org/ac/Adult/ui/stg2SummaryRpt?doc=AC150 , though it states AOO is not fully clear.

Severity

 Options

Embryonic lethal - presence of a pathogenic variant or variants is not compatible with life. The penetrance must be complete.
Severe - presence of a pathogenic variant or variant(s) results in significantly reduced fitness. The penetrance must be complete or high.
Moderate - significant morbidity or mortality due to clinical features, but fitness may not be reduced, or penetrance is reduced.
Mild - Presence of a variant or variant(s) is not associated with reduced fitness, no significant morbidity or mortality, and/or penetrance is low.
None - presence of a variant results in no phenotype. An example is recessive disorders in which no phenotype is reported in carriers.

Moderate

Clinical Features

Multiple paragangliomas and/or pheochromocytomas

Sources:

Gene SOPs & Notes

No ClinGen VCEP with guidelines. Reviewed variants in ClinVar for red flags

Curation Summary:

 Examples

- The @GENE@ is associated with @inheritance pattern@ @condition@, which is characterized by @clinical features@ (PMIDs).

- Variable expression or severity:
The severity and expressivity of the disorder is highly variable, even within families.
- If multiple conditions associated with the gene:
It has also been associated with @inheritance pattern@ @condition@, which is characterized by @clinical features@ (PMIDs).

- Limited evidence gene: The PCNA gene has been reported in individuals with early onset autosomal recessive ataxia (PMID: 33426167, 24911150), however, evidence supporting this gene-dsiease relationship is limited

The SDHAF2 gene is associated with autosomal dominant hereditary paraganglioma and pheochromocytoma, which is characterized by increased risk of paragangliomas and pheochromocytomas that are more likely to present at younger ages, be multifocal, bilateral or recurrent and present synchronously compared to sporadic disease (PMID: 20301715). Penetrance is age related with a parent-of-origin effect, with higher risk observed in individuals with paternally inherited alleles (PMID: 26067997, 19628817).

Case ID, Curator name, Date, Jira ticket link

Andrea Oza 06.30.2023 CIT-130 - Getting issue details... STATUS

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