NALF1-IT1

Chr 13

NALF1 intronic transcript 1

Also known as: FAM155A-IT1

I cannot provide a clinical summary for NALF1-IT1 as no supporting data about this gene's protein function, associated diseases, or inheritance pattern has been provided. A clinical summary requires specific information about what the protein does, what conditions result from mutations, and the inheritance pattern to be clinically useful for child neurologists.

Clinical SummaryNALF1-IT1
📋
ClinVar Variants
43 unique Pathogenic / Likely Pathogenic· 2 VUS of 47 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

47 submitted variants in ClinVar

Classification Summary

Pathogenic43
VUS2
Likely Benign1
Benign1
43
Pathogenic
2
VUS
1
Likely Benign
1
Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
43
Likely Pathogenic
0
VUS
2
Likely Benign
1
Benign
1
Total47

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

NALF1-IT1 · 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 →

No publications found for NALF1-IT1