FOXP4 - forkhead box P4 Gene
Also Known as hFKHLA
Species: Homo sapiens
About FOXP4
This gene has 9 transcripts (splice variants), 190 orthologues, 4 paralogues and is associated with 1 phenotype. Ubiquitous expression in stomach (RPKM 7.0), testis (RPKM 4.6) and 25 other tissues.
Summary
This gene belongs to subfamily P of the forkhead box (FOX) transcription factor family. Forkhead box transcription factors play important roles in the regulation of tissue- and cell type-specific gene transcription during both development and adulthood. Many members of the forkhead box gene family, including members of subfamily P, have roles in mammalian oncogenesis. This gene may play a role in the development of tumors of the kidney and larynx. Alternative splicing of this gene produces multiple transcript variants, some encoding different isoforms. [provided by RefSeq, Jul 2008]
FOXP4 Products (6)
| mRNA | Protein | Name |
|---|---|---|
| NM_001012426.2 | NP_001012426.1 | forkhead box protein P4 isoform 1 |
| NM_001012427.2 | NP_001012427.1 | forkhead box protein P4 isoform 3 |
| NM_001405824.1 | NP_001392753.1 | forkhead box protein P4 isoform 4 |
| NM_001405825.1 | NP_001392754.1 | forkhead box protein P4 isoform 5 |
| NM_001405826.1 | NP_001392755.1 | forkhead box protein P4 isoform 6 |
| NM_138457.3 | NP_612466.1 | forkhead box protein P4 isoform 2 |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
19907493 | GOA |
FOXP4 Protein Structure
Forkhead: Forkhead domain (467 - 546)
- 0
- 200
- 400
- 600
- 680 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
forkhead box protein P4 |
|
FOXP4 Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
FOXP4 | Q8IVH2 | FOXP2 | Homo sapiens | O15409 | 25609649 | |
|
Intra
|
FOXP4 | Q8IVH2 | FOXP1 | Homo sapiens | Q9H334 | 25609649 |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Ventricular Septal Defect |
|
|
| Sensorineural Hearing Loss |
|
|
| Intellectual Disability-Severe Speech Delay-Mild Dysmorphism Syndrome |
|
|
| Speech Disorder |
|
Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Felis catus | FOXP4 | VGNC | VGNC:62346 |
| Macaca mulatta | FOXP4 | VGNC | VGNC:72755 |
| Mus musculus | FOXP4 | MGD | MGI:1921373 |
| Canis familiaris | FOXP4 | VGNC | VGNC:40968 |
| Rattus norvegicus | FOXP4 | RGD | RGD:1311386 |
| Bos taurus | FOXP4 | VGNC | VGNC:29103 |
| Others | FOXP4 | NCBI |