MHC region gene
Evidence from:
primary |
all sources
Related entities (8)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| FINEMAP | associated_with | MHC region | — | 1 |
| MHC region | associated_with | associated SNPs | — | 1 |
| MHC region | risk_factor_for | bipolar disorder | — | 1 |
| MHC region | associated_with | Brainstorm Consortium | — | 1 |
| MHC region | associated_with | immune function | — | 1 |
| MHC region | associated_with | major depressive disorder | — | 1 |
| MHC region | associated_with | schizophrenia | — | 1 |
| MHC region | associated_with | UK Biobank | — | 1 |
Mentioned in (24)
Papers in which this entity is mentioned.
- Robust and accurate Bayesian inference of genome-wide genealogies for hundreds of genomes. (2025)
- Genome-wide association testing beyond SNPs. (2025)
- Immune selection determines tumor antigenicity and influences response to checkpoint inhibitors. (2023)
- Cross-tissue transcriptome-wide association studies identify susceptibility genes shared between schizophrenia and inflammatory bowel disease. (2022)
- Mapping genomic loci implicates genes and synaptic biology in schizophrenia. (2022)
- Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. (2021)
- Graph-based genome alignment and genotyping with HISAT2 and HISAT-genotype. (2019)
- Sex differences in the genetic architecture of obsessive-compulsive disorder. (2019)
- Rare variant phasing using paired tumor:normal sequence data. (2019)
- The GenomeAsia 100K Project enables genetic discoveries across Asia. (2019)
- Polygenic risk for neuropsychiatric disease and vulnerability to abnormal deep grey matter development. (2019)
- Comprehensive analysis of structural variants in breast cancer genomes using single molecule sequencing (2019)
- Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types. (2018)
- A SNP panel for identification of DNA and RNA specimens. (2018)
- Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. (2018)
- Fast and accurate HLA typing from short-read next-generation sequence data with xHLA. (2017)
- High-Accuracy HLA Type Inference from Whole-Genome Sequencing Data Using Population Reference Graphs. (2016)
- Detecting Genomic Signatures of Natural Selection with Principal Component Analysis: Application to the 1000 Genomes Data. (2016)
- The IPD and IMGT/HLA database: allele variant databases. (2015)
- A gene-based association method for mapping traits using reference transcriptome data. (2015)
- Heritability and genomics of gene expression in peripheral blood. (2014)
- Rapid genome mapping in nanochannel arrays for highly complete and accurate de novo sequence assembly of the complex Aegilops tauschii genome. (2013)
- Fast computation and applications of genome mappability. (2012)
Merged raw entities (7)
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 |
|---|---|---|---|
| hla region | gene | 10 | 12 |
| major histocompatibility complex | gene | 7 | 7 |
| mhc region | gene | 5 | 7 |
| mhc region | anatomy | 3 | 3 |
| chr6:24–34 mb on hg19 | gene | — | — |
| chr6:31-33 mb | gene | — | — |
| extended mhc region | gene | — | — |