protein-coding gene gene
Evidence from:
primary |
all sources
Related entities (2)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| associated SNPs | targets | protein-coding gene | — | 1 |
| SNP | interacts_with | protein-coding gene | — | 1 |
Mentioned in (28)
Papers in which this entity is mentioned.
- Annotating the genome at single-nucleotide resolution with DNA foundation models. (2025)
- Massively parallel reporter assay investigates shared genetic variants of eight psychiatric disorders. (2025)
- Genome-wide association testing beyond SNPs. (2025)
- A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies. (2025)
- Transcription start sites experience a high influx of heritable variants fueled by early development. (2025)
- Global impact of unproductive splicing on human gene expression. (2024)
- Detection and analysis of complex structural variation in human genomes across populations and in brains of donors with psychiatric disorders. (2024)
- Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder. (2024)
- A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies. (2023)
- Item-Level Genome-Wide Association Study of the Alcohol Use Disorders Identification Test in Three Population-Based Cohorts. (2022)
- Spatially resolved whole transcriptome profiling in human and mouse tissue using Digital Spatial Profiling. (2022)
- Inferring gene expression from cell-free DNA fragmentation profiles. (2022)
- Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes. (2021)
- Reciprocal monoallelic expression of ASAR lncRNA genes controls replication timing of human chromosome 6. (2020)
- The Ensembl gene annotation system. (2016)
- Tools and best practices for data processing in allelic expression analysis. (2015)
- Comparison of RNA-seq and microarray-based models for clinical endpoint prediction. (2015)
- The landscape of long noncoding RNAs in the human transcriptome. (2015)
- The use of exome capture RNA-seq for highly degraded RNA with application to clinical cancer sequencing. (2015)
- Cancer genome landscapes. (2013)
- Signatures of mutational processes in human cancer. (2013)
- Landscape of transcription in human cells. (2012)
- Mutational processes molding the genomes of 21 breast cancers. (2012)
- Fast computation and applications of genome mappability. (2012)
- An integrated encyclopedia of DNA elements in the human genome. (2012)
- Differential expression in RNA-seq: a matter of depth. (2011)
- Splicing factor SFRS1 recognizes a functionally diverse landscape of RNA transcripts. (2009)
- An RNA code for the FOX2 splicing regulator revealed by mapping RNA-protein interactions in stem cells. (2009)
Merged raw entities (5)
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 |
|---|---|---|---|
| protein-coding genes | gene | 29 | 42 |
| protein-coding gene | gene | 19 | 27 |
| protein coding genes | gene | 8 | 8 |
| protein-coding loci | gene | 1 | 1 |
| protein-coding dna | gene | — | — |