Gene entry

UPF3B

UPF3B regulator of nonsense mediated mRNA decay

Chromosome: X
Cytoband: Xq24
Variants (rsID): 8

UPF3B is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xq24). Its official name is “UPF3B regulator of nonsense mediated mRNA decay”. The reference table lists 8 variants (rsID) for this gene.

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Clinically classified variants

1 reference-table entries with clinical significance.

rs143538947Conflicting interpretationssingle nucleotide variantSyndromic X-linked intellectual disability 14|History of neurodevelopmental disorder

Other listed variants

rs2239963
rs2285552
rs4825677
rs5910686
rs17261236
rs111603369
rs139646537

Public references

NCBI Gene
Ensembl
ClinVar

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.