NALT1

Chr 9

NOTCH1 associated lncRNA in T cell acute lymphoblastic leukemia 1

Also known as: LINC01573, MIR4674HG, NALT, TCONS_l2_00029132

I notice that no specific information about the NALT1 gene has been provided below your request - there's no data about protein function, associated diseases, inheritance patterns, or constraint metrics. Without this supporting information, I cannot write a clinical summary following your strict rule to use only the provided data. Could you please provide the relevant gene information for NALT1?

Clinical SummaryNALT1
📋
ClinVar Variants
49 unique Pathogenic / Likely Pathogenic of 49 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

49 submitted variants in ClinVar

Classification Summary

Pathogenic48
Likely Pathogenic1
48
Pathogenic
1
Likely Pathogenic

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
48
Likely Pathogenic
1
VUS
0
Likely Benign
0
Benign
0
Total49

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

NALT1 · 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 →
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC