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Literature record

A missense variant in the PACS2 gene cause Epileptic Encephalopathy and seizures in Saudi family.

PMID 38545008 | PMCID PMC10963950 | DOI 10.12669/pjms.40.4.8707 · Pakistan journal of medical sciences · 2024

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We identified the PACS2 gene responsible for the multifunctional sorting protein that play a role in nuclear gene expression as well as pathway traffic regulation. Diseases associated with PACS2 include early infantile epileptic encephalopathy (EIEE66), alacrima, achalasia, and mental retardation syndrome. Whole exome sequencing (WES) technique was used for the identification of variants that may lead to the disease. We identified a consanguineous Saudi family segregating developmental delay, mental retardation and epilepsy. Our results showed a heterozygous missense variant PACS2 gene leading to intellectual disability, epilepsy and cause epileptic encephalopathies (EIEE66) disorder. WES data was analyzed and identified variants were further confirmed by Sanger sequencing validation technique. We identified a heterozygous missense c.625G>A p.Glu209Lys in exon-6 of PACS2. The detected heterozygous mutation in the exon-6 region of PACS2 gene change the protein features and may cause disease. Further, explain the possibility that PACS2 gene play important role to cause intellectual disability, epilepsy and epileptic encephalopathies in this Saudi family.

Validated evidence

TypeEntitySource evidenceConfidenceExtractor
genePACS2“A missense variant in the PACS2 gene cause Epileptic Encephalopathy and seizures in Saudi family.”0.98hgnc_dict_v1
phenotypedevelopmental delay“We identified a consanguineous Saudi family segregating developmental delay, mental retardation and epilepsy.”0.98phenotype_alias_lexicon_v2
phenotypeepilepsy“A missense variant in the PACS2 gene cause Epileptic Encephalopathy and seizures in Saudi family.”0.93phenotype_alias_lexicon_v2
phenotypeintellectual disability“Diseases associated with PACS2 include early infantile epileptic encephalopathy (EIEE66), alacrima, achalasia, and mental retardation syndrome.”0.93phenotype_alias_lexicon_v2
populationSaudi Arabia“A missense variant in the PACS2 gene cause Epileptic Encephalopathy and seizures in Saudi family. We identified a consanguineous Saudi family segregating developmental delay, mental retardation and epilepsy. Further, explain the possibility that PACS2 gene play important role to cause intellectual disability, epilepsy and epileptic encephalopathies in this Saudi family.”0.95saudi_context_rules_v1
variantc.625G>A“We identified a heterozygous missense c.625G>A p.Glu209Lys in exon-6 of PACS2.”0.95hgvs_regex_v1
variantp.Glu209Lys“We identified a heterozygous missense c.625G>A p.Glu209Lys in exon-6 of PACS2.”0.95hgvs_regex_v1