Genetic Information
Gene & Transcript Details
| ID | Status | Details |
|---|---|---|
| NM_005089.1 | Alternative | 1488 nt | 25–1473 |
| NM_005089.3 | RefSeq Select | 1512 nt | 46–1494 |
| NM_005089.2 | Alternative | 1609 nt | 25–1473 |
| NM_005089.4 | MANE Select | 1479 nt | 13–1461 |
Variant Details
Clinical & Population Data
Population Frequency
gnomADClinVar
Open""
COSMIC Somatic Evidence
Open
Functional Impact & Domains
Functional Domain
The ZRSR2 R126* variant is a truncating mutation that results in C-terminally truncated proteins. Functional studies have demonstrated that knockdown of ZRSR2 leads to aberrant splicing and global intron retention, indicating its critical role in splicing U12-type introns. Additionally, knockdown in human hematopoietic stem cells results in reduced proliferation, impaired colony formation, and differentiation defects. These findings support a damaging effect of the ZRSR2 R126* variant, contributing to defective differentiation due to splicing defects.
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Computational Analysis
Pathogenicity Predictions
SpliceAISpliceAI Scores
Window: ±500bp| Effect Type | Score | Position |
|---|---|---|
| Acceptor Loss (AL) | 0.1 | -61 bp |
| Donor Loss (DL) | 0.04 | 23 bp |
| Acceptor Gain (AG) | 0.0 | -60 bp |
| Donor Gain (DG) | 0.0 | 76 bp |
VCEP Guidelines
Applied ACMG/AMP Criteria (VCEP Specific)
PVS1 (Very Strong)
According to standard ACMG guidelines the rule for PVS1 is: "Null variant in a gene where loss of function (LoF) is a known mechanism of disease (e.g., nonsense, frameshift, canonical ±1 or 2 splice sites, initiation codon, single exon deletion in a LoF gene)". The evidence for this variant shows: c.376C>T (R126*) introduces a premature stop codon predicted to result in loss of function of ZRSR2. Therefore, this criterion is applied at Very Strong strength because it is a null variant in a gene where LoF is a known mechanism of disease.
PS1 (Not Applied)
According to standard ACMG guidelines the rule for PS1 is: "Same amino acid change as a known pathogenic variant but different nucleotide change". The evidence for this variant shows: no other nucleotide change at R126 has been reported as pathogenic. Therefore, this criterion is not applied.
PS2 (Not Applied)
According to standard ACMG guidelines the rule for PS2 is: "De novo (both maternity and paternity confirmed) in a patient with the disease and no family history". The evidence for this variant shows: no de novo data are available. Therefore, this criterion is not applied.
PS3 (Strong)
According to standard ACMG guidelines the rule for PS3 is: "Well-established functional studies supportive of a damaging effect on the gene or gene product". The evidence for this variant shows: functional studies demonstrate that R126* leads to aberrant splicing, global intron retention, and impaired hematopoietic differentiation. Therefore, this criterion is applied at Strong strength because well-established functional assays show a damaging effect.
PS4 (Not Applied)
According to standard ACMG guidelines the rule for PS4 is: "Prevalence in affected individuals significantly increased compared with controls". The evidence for this variant shows: no case–control data demonstrating enrichment in affected individuals. Therefore, this criterion is not applied.
PM1 (Not Applied)
According to standard ACMG guidelines the rule for PM1 is: "Located in a mutational hot spot or well-established functional domain without benign variation". The evidence for this variant shows: no defined mutational hotspot or specific functional domain annotated at R126. Therefore, this criterion is not applied.
PM2 (Moderate)
According to standard ACMG guidelines the rule for PM2 is: "Absent from controls (or at extremely low frequency if recessive)". The evidence for this variant shows: c.376C>T is not observed in gnomAD or other population databases. Therefore, this criterion is applied at Moderate strength because it is absent from population controls.
PM3 (Not Applied)
According to standard ACMG guidelines the rule for PM3 is: "Detected in trans with a pathogenic variant (for recessive disorders)". The evidence for this variant shows: no data on trans configuration with another variant. Therefore, this criterion is not applied.
PM4 (Not Applied)
According to standard ACMG guidelines the rule for PM4 is: "Protein length changes due to in-frame deletions/insertions or stop-loss variants". The evidence for this variant shows: this is a nonsense variant, not an in-frame indel or stop-loss. Therefore, this criterion is not applied.
PM5 (Not Applied)
According to standard ACMG guidelines the rule for PM5 is: "Novel missense change at an amino acid residue where a different pathogenic missense change has been seen". The evidence for this variant shows: this is a nonsense change, not a missense. Therefore, this criterion is not applied.
PM6 (Not Applied)
According to standard ACMG guidelines the rule for PM6 is: "Assumed de novo, but without confirmation of paternity and maternity". The evidence for this variant shows: no de novo assumption data. Therefore, this criterion is not applied.
PP1 (Not Applied)
According to standard ACMG guidelines the rule for PP1 is: "Co-segregation with disease in multiple affected family members". The evidence for this variant shows: no segregation data available. Therefore, this criterion is not applied.
PP2 (Not Applied)
According to standard ACMG guidelines the rule for PP2 is: "Missense variant in a gene with a low rate of benign missense variation and where missense variants are a common mechanism of disease". The evidence for this variant shows: this is a nonsense variant, not a missense. Therefore, this criterion is not applied.
PP3 (Not Applied)
According to standard ACMG guidelines the rule for PP3 is: "Multiple lines of computational evidence support a deleterious effect on the gene or gene product". The evidence for this variant shows: computational predictions are mixed/benign (CADD 7.62, SpliceAI 0.1). Therefore, this criterion is not applied.
PP4 (Not Applied)
According to standard ACMG guidelines the rule for PP4 is: "Patient's phenotype or family history highly specific for a disease with a single genetic etiology". The evidence for this variant shows: no specific phenotype correlation provided. Therefore, this criterion is not applied.
PP5 (Not Applied)
According to standard ACMG guidelines the rule for PP5 is: "Reputable source reports variant as pathogenic, but without accessible evidence". The evidence for this variant shows: not found in ClinVar or other reputable sources. Therefore, this criterion is not applied.
BA1 (Not Applied)
According to standard ACMG guidelines the rule for BA1 is: "Allele frequency is too high for the disorder (based on population data)". The evidence for this variant shows: allele frequency is zero. Therefore, this criterion is not applied.
BS1 (Not Applied)
According to standard ACMG guidelines the rule for BS1 is: "Allele frequency is greater than expected for the disorder". The evidence for this variant shows: allele frequency is zero. Therefore, this criterion is not applied.
BS2 (Not Applied)
According to standard ACMG guidelines the rule for BS2 is: "Observed in healthy individuals with full penetrance expected at an early age". The evidence for this variant shows: no data in healthy cohorts. Therefore, this criterion is not applied.
BS3 (Not Applied)
According to standard ACMG guidelines the rule for BS3 is: "Well-established functional studies show no damaging effect on protein function or splicing". The evidence for this variant shows: functional studies demonstrate damaging effect. Therefore, this criterion is not applied.
BS4 (Not Applied)
According to standard ACMG guidelines the rule for BS4 is: "Lack of segregation in affected family members". The evidence for this variant shows: no segregation data. Therefore, this criterion is not applied.
BP1 (Not Applied)
According to standard ACMG guidelines the rule for BP1 is: "Missense variant in a gene where only LoF causes disease". The evidence for this variant shows: this is a nonsense variant. Therefore, this criterion is not applied.
BP2 (Not Applied)
According to standard ACMG guidelines the rule for BP2 is: "Observed in trans with a pathogenic variant for dominant disorders or in cis with a pathogenic variant". The evidence for this variant shows: no phase data. Therefore, this criterion is not applied.
BP3 (Not Applied)
According to standard ACMG guidelines the rule for BP3 is: "In-frame deletions/insertions in a repetitive region without known function". The evidence for this variant shows: this is a nonsense variant. Therefore, this criterion is not applied.
BP4 (Supporting)
According to standard ACMG guidelines the rule for BP4 is: "Multiple lines of computational evidence suggest no impact on gene or gene product". The evidence for this variant shows: CADD score of 7.62 (benign) and SpliceAI maximum score of 0.1 (below threshold). Therefore, this criterion is applied at Supporting strength because computational predictions are consistently benign.
BP5 (Not Applied)
According to standard ACMG guidelines the rule for BP5 is: "Variant found in a case with an alternate molecular basis for disease". The evidence for this variant shows: no alternate molecular diagnosis. Therefore, this criterion is not applied.
BP6 (Not Applied)
According to standard ACMG guidelines the rule for BP6 is: "Reputable source reports variant as benign, but without accessible evidence". The evidence for this variant shows: no such reports. Therefore, this criterion is not applied.
BP7 (Not Applied)
According to standard ACMG guidelines the rule for BP7 is: "Synonymous variant with no predicted impact on splicing". The evidence for this variant shows: this is a nonsense variant. Therefore, this criterion is not applied.