| GENE NAME | FOXP1 |
| CHROMOSOME | 3 |
| ENSEMBL ID | None |
| ENTREZ ID | ENSG00000114861 |
| UNIPROT ACCESSION NUMBER | A0A0B4J2F3 |
| GO MOLECULAR FUNCTION | ['core promoter sequence-specific DNA binding', 'RNA polymerase II cis-regulatory region sequence-specific DNA binding', 'DNA-binding transcription repressor activity, RNA polymerase II-specific', 'protein self-association', 'DNA-binding transcription factor activity, RNA polymerase II-specific', 'sequence-specific double-stranded DNA binding', 'protein binding', 'metal ion binding', 'identical protein binding', 'androgen receptor binding'] |
| ESSENTIAL IN MOUSE | Essential |
| PATHWAYS | hsa05206; hsa05206 |
| 3 combinations linked to FOXP1 | OLI1528; OLI1246; OLI1554 |
| 3 variants linked to FOXP1 | FOXP1:c.16T>C, p.Phe6Leu; FOXP1:c.1762G>A, p.Ala588Thr; FOXP1:c.1501G>A, p.Ala501Thr |
| 3 diseases linked to FOXP1 | 46,XY disorder of sex development; Progressive non-fluent aphasia; Corticobasal syndrome |