CELF4 gene
Evidence from:
primary |
all sources
Related entities (4)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| CELF4 | risk_factor_for | autism spectrum disorder | — | 1 |
| CELF4 | risk_factor_for | epilepsy | — | 1 |
| CELF4 | expressed_in | interneuron | — | 1 |
| CELF4 | regulates | Scn8a | — | 1 |
Mentioned in (3)
Papers in which this entity is mentioned.
- Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions. (2021)
- Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. (2018)
- Assembly of functionally integrated human forebrain spheroids. (2017)
Merged raw entities (2)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| celf4 | gene | 3 | 4 |
| cugbp elav-like family member 4 | gene | — | — |