ZPLD2P

Chr 1

zona pellucida like domain containing 2, pseudogene

I cannot provide a clinical summary for ZPLD2P as no functional, phenotypic, or inheritance information has been provided in the data. Without details about the protein function, associated diseases, or inheritance pattern, I cannot write a clinically accurate summary following the specified guidelines.

Clinical SummaryZPLD2P
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ClinVar Variants
2 unique Pathogenic / Likely Pathogenic· 1 VUS of 3 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

3 submitted variants in ClinVar

Classification Summary

Pathogenic2
VUS1
2
Pathogenic
1
VUS

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
2
Likely Pathogenic
0
VUS
1
Likely Benign
0
Benign
0
Total3

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

ZPLD2P · protein map & ClinVar variants

Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.

3D Protein StructureAlphaFold

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

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Clinical Literature
Open Research Assistant →

No publications found for ZPLD2P