FAM224B

Chr Y

family with sequence similarity 224 member B

Also known as: LINC00230B, NCRNA00230B

This locus is transcribed but does not appear to encode a protein and consists of two identical copies located in a palindromic region on chromosome Y. No disease associations have been established for FAM224B mutations. Given its location on the Y chromosome, any potential effects would follow paternal inheritance patterns.

ResearchSummary from RefSeq
Clinical SummaryFAM224B
📋
ClinVar Variants
27 unique Pathogenic / Likely Pathogenic· 4 VUS of 35 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

35 submitted variants in ClinVar

Classification Summary

Pathogenic25
Likely Pathogenic2
VUS4
Likely Benign3
Conflicting1
25
Pathogenic
2
Likely Pathogenic
4
VUS
3
Likely Benign
1
Conflicting

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
25
Likely Pathogenic
2
VUS
4
Likely Benign
3
Benign
0
Conflicting
1
Total35

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

FAM224B · 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.

Search ClinicalTrials.gov →
Clinical Literature
Open Research Assistant →
Full-Text Mentions
NLP-detected gene mentions in article bodies · via PubTator3
PubTator3
Top 2 full-text resultsSearch PubTator3 ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found