FAM74A7

Chr 9

family with sequence similarity 74 member A7

I cannot write a clinical gene summary for FAM74A7 because no information about this gene's protein function, associated diseases, inheritance pattern, or mechanism of pathogenicity was provided in your prompt. To create an accurate clinical summary following your guidelines, I would need specific data about what the FAM74A7 protein does, what neurological conditions result from mutations in this gene, and how these mutations cause disease.

DNmechanism
Clinical SummaryFAM74A7
📋
ClinVar Variants
20 unique Pathogenic / Likely Pathogenic of 23 total submissions
Some data sources returned errors (1)

gnomad: Error: Gene not found

Population Genetics & Constraint

Constraint data not available from gnomAD.

DN
0.6938th %ile
GOF
0.6248th %ile
LOF
0.4529th %ile

The highest-scoring mechanism for this gene is dominant-negative.

DNprediction above median

Note: In-silico variant effect predictors (SIFT, PolyPhen, REVEL, CADD) may underestimate pathogenicity of missense variants in genes with GOF or DN mechanisms. Consider functional evidence and clinical context.

Predictions from Badonyi M, Marsh JA. PLoS ONE. 2024;19(8):e0307312.

ClinVar Variant Classifications

23 submitted variants in ClinVar

Classification Summary

Pathogenic19
Likely Pathogenic1
Likely Benign1
Benign2
19
Pathogenic
1
Likely Pathogenic
1
Likely Benign
2
Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
19
Likely Pathogenic
1
VUS
0
Likely Benign
1
Benign
2
Total23

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

FAM74A7 · 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