NUTM2F
Chr 9NUT family member 2F
Also known as: FAM22F, NUTMF
I notice that while you've provided the gene name NUTM2F and its constraint metrics (pLI and LOEUF scores), you haven't included the essential clinical information needed to write a summary according to your specifications. To write the 2-3 sentence clinical summary you've requested, I would need information about: - The protein's specific function - Associated diseases/phenotypes from mutations - Inheritance pattern - Mechanism of pathogenicity Could you please provide the clinical data for NUTM2F so I can write an appropriate summary for your pediatric neurogenetics portal?
Population Genetics & Constraint
gnomAD v4 — loss-of-function & missense intolerance
Highly tolerant — LoF variants common in population
Tolerant to missense variation
ClinVar Variant Classifications
0 submitted variants in ClinVar
Protein Context — Lollipop Plot
NUTM2F · protein map & ClinVar variants
Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.
3D Protein StructureAlphaFold
External Resources
Links to major genomics databases and tools
Clinical Trials
Active and recruiting trials from ClinicalTrials.gov
No active trials found for this gene.
Search ClinicalTrials.gov →No open access results found
External Resources
Links to major genomics databases and tools