UPF3B
HGNC:20439 · SaudiVarKB evidence summary derived from retained literature mentions.
2Gene mentions
2Publications
0Linked variants
3Associated phenotypes
Associated phenotypes
Co-mentioned in UPF3B publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| autism spectrum disorder | HP:0000729 | 2 | 2 |
| intellectual disability | HP:0001249 | 1 | 1 |
| neurodevelopmental disorder | HP:0012759 | 1 | 1 |
Linked variants
Variants normalized to UPF3B| Variant | HGVS / rsID | Articles | Mentions |
|---|
No normalized variants are linked to this gene.
Population context
Reported in the same publications| Country / region | Group | Cohort | Articles |
|---|
No structured population context is available.
Supporting publications
2 records- 2026Network-Based Prioritization of Network-Peripheral Gene Modules in Autism Spectrum Disorder Using Integrative Transcriptomic and Proteomic Data.Journal of molecular neuroscience : MNPubMed ↗
- 2015Full UPF3B function is critical for neuronal differentiation of neural stem cells.Molecular brainPubMed ↗