FAM90A20

Chr 8

family with sequence similarity 90 member A20

Also known as: FAM90A20P

FAM90A20 belongs to subfamily II of the primate-specific FAM90A gene family, which originated from multiple duplications and rearrangements (Bosch et al., 2007 [PubMed 17684299]). For background information on the FAM90A gene family, as well as information on the evolution of FAM90A genes, see FAM90A1 (MIM 613041).[supplied by OMIM, Oct 2009]

0
Active trials
35
Pathogenic / LP
72
ClinVar variants
0
Pubs (1 yr)
Missense Z
LOEUF
Clinical SummaryFAM90A20
📋
ClinVar Variants
35 Pathogenic / Likely Pathogenic of 72 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

72 submitted variants in ClinVar

Classification Summary

Pathogenic35
Likely Benign3
Benign34
35
Pathogenic
3
Likely Benign
34
Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
35
Likely Pathogenic
0
VUS
0
Likely Benign
3
Benign
34
Total72

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

FAM90A20 · protein map & ClinVar variants

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

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →
Clinical Literature
Landmark / reviewRecent case evidence
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found