FAM230J

Chr 22

family with sequence similarity 230 member J

Also known as: LINC01660

NCBI Gene: 729461ENSG00000274044
152
ClinVar variants
143
Pathogenic / LP
—
pLI score
0
Active trials
Clinical Summary— FAM230J
📋
ClinVar Variants
143 Pathogenic / Likely Pathogenic· 3 VUS of 152 total submissions
Some data sources returned errors (1)

gnomad: Error: Gene not found

Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

152 submitted variants in ClinVar

ClinVar

Classification Summary

Pathogenic143
VUS3
Likely Benign6
143
Pathogenic
3
VUS
6
Likely Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
————143
Likely Pathogenic
————0
VUS
————3
Likely Benign
————6
Benign
————0
Total—152

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

FAM230J · 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 FAM230J

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