OPCML gene
Evidence from:
primary |
all sources
Related entities (4)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| OPCML | risk_factor_for | autism spectrum disorder | — | 1 |
| OPCML | risk_factor_for | developmental delay | — | 1 |
| OPCML | associated_with | schizophrenia | — | 1 |
| OPCML | associated_with | synaptogenesis | — | 1 |
Mentioned in (3)
Papers in which this entity is mentioned.
- Neural cell adhesion molecule Negr1 deficiency in mouse results in structural brain endophenotypes and behavioral deviations related to psychiatric disorders. (2019)
- Single-Cell Profiling of an In Vitro Model of Human Interneuron Development Reveals Temporal Dynamics of Cell Type Production and Maturation. (2017)
- Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk. (2009)
Merged raw entities (1)
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 |
|---|---|---|---|
| opcml | gene | 3 | 4 |