CNTN4 gene
Evidence from:
primary |
all sources
Related entities (3)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| Bcl11b | regulates | CNTN4 | — | 1 |
| CNTN4 | associated_with | autism spectrum disorder | — | 1 |
| CNTN4 | risk_factor_for | autism spectrum disorder | — | 1 |
Mentioned in (6)
Papers in which this entity is mentioned.
- Expansion of Schizophrenia Gene Network Knowledge Using Machine Learning Selected Signals From Dorsolateral Prefrontal Cortex and Amygdala RNA-seq Data. (2022)
- TGF-β/Smad3 Signalling Modulates GABA Neurotransmission: Implications in Parkinson's Disease. (2020)
- The role of BAF (mSWI/SNF) complexes in mammalian neural development. (2014)
- Common DNA methylation alterations in multiple brain regions in autism. (2014)
- CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012)
- Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011)
Merged raw entities (4)
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 |
|---|---|---|---|
| cntn4 | gene | 5 | 5 |
| big2 | gene | 1 | 1 |
| contactin 4 | gene | — | — |
| contactin4 | gene | — | — |