Gene | FOXP1 |
Biotype | protein_coding |
Description | forkhead box P1 |
Synonyms | 12CC4; HSPC215; MFH; QRF1; hFKH1B; |
Location | chr3:70954693-71583989 |
Ensembl | ENSG00000114861 |
Entrez | 27086 |
Hgnc | 3823 |
Hprd | 18518 |
Mim | 605515 |
Swissprot | Q9H334 |
Trembl | Q548T7 H0Y882 E9PFD3 G5E965 C9J0F0 C9J5T4 A0A087X2G3 C9IYY1 A0A087WVT2 A0A0B4J2F3 A0A087X299 |
Vega | OTTHUMG00000158803 |
Studies containing regions of association that span this gene are shown below. Please note that when making comparisons across studies, that they may vary in terms of size, genotyping platform, and exclusion criteria. If the 'Odds Ratio' is less than 1 then the region is protective (alleles are marked as blue) otherwise it is susceptible (alleles marked as red).
Study | Publication | Disease | Region | Marker | Alleles | P-value | OR | MAF | Gene(s) |
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Gene sets for the gene FOXP1 are derived from MSigDB
Name | Genes |
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Organism | Gene | Phenotype | Resources |
---|---|---|---|
Mouse | MGI:1914004 | MGI:1914004 | IMPC |