NLGN4X gene
Evidence from:
primary |
all sources
Related entities (3)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| NLGN4X | risk_factor_for | autism | — | 1 |
| NLGN4X | risk_factor_for | autism spectrum disorder | — | 1 |
| NLGN4X | expressed_in | brain | — | 1 |
Mentioned in (4)
Papers in which this entity is mentioned.
- Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism. (2012)
- CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012)
- Spatio-temporal transcriptome of the human brain. (2011)
- Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. (2011)
Merged raw entities (3)
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 |
|---|---|---|---|
| nlgn4x | gene | 4 | 9 |
| neuroligin 4x | gene | — | — |
| ngln4x | gene | — | — |