CXORF51B

Chr X

chromosome X open reading frame 51B

Also known as: CXorf51A

NCBI Gene: 100133053ENSG00000235699UniProt: P0DPH9
100
ClinVar variants
93
Pathogenic / LP
—
pLI score
0
Active trials
Clinical Summary— CXORF51B
📋
ClinVar Variants
93 Pathogenic / Likely Pathogenic· 6 VUS of 100 total submissions

Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

100 submitted variants in ClinVar

ClinVar

Classification Summary

Pathogenic90
Likely Pathogenic3
VUS6
Likely Benign1
90
Pathogenic
3
Likely Pathogenic
6
VUS
1
Likely Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
————90
Likely Pathogenic
————3
VUS
————6
Likely Benign
————1
Benign
————0
Total—100

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

CXORF51B · protein map & ClinVar variants

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

OMIM — Genotype-Phenotype

OMIM

No OMIM entries found.

Clinical Literature
Landmark / reviewRecent case evidence

No publications found for CXORF51B

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →

External Resources

Links to major genomics databases and tools