Protein family
The protein has not catalytic activity
Protein sequence
Protein function
Catalytic activity
PDB | Resolution (Å) | PDB name |
---|---|---|
2KIU | Solution structure and backbone dynamics of the DNA-binding domain of FOXP1: Insight into its domain swapping |
GO ontology | GO term | GO description |
---|---|---|
Biological Process | GO:0006974 | DNA damage response |
Biological Process | GO:0061470 | T follicular helper cell differentiation |
Biological Process | GO:0071356 | cellular response to tumor necrosis factor |
Biological Process | GO:0042118 | endothelial cell activation |
Biological Process | GO:0042116 | macrophage activation |
Biological Process | GO:0042117 | monocyte activation |
Biological Process | GO:0002903 | negative regulation of B cell apoptotic process |
Biological Process | GO:0045892 | negative regulation of DNA-templated transcription |
Biological Process | GO:0060766 | negative regulation of androgen receptor signaling pathway |
Biological Process | GO:0061052 | negative regulation of cell growth involved in cardiac muscle cell development |
Biological Process | GO:0010629 | negative regulation of gene expression |
Biological Process | GO:0036035 | osteoclast development |
Biological Process | GO:0030316 | osteoclast differentiation |
Biological Process | GO:0050861 | positive regulation of B cell receptor signaling pathway |
Biological Process | GO:0010595 | positive regulation of endothelial cell migration |
Biological Process | GO:1905206 | positive regulation of hydrogen peroxide-induced cell death |
Biological Process | GO:0032745 | positive regulation of interleukin-21 production |
Biological Process | GO:0048661 | positive regulation of smooth muscle cell proliferation |
Biological Process | GO:2000341 | regulation of chemokine (C-X-C motif) ligand 2 production |
Biological Process | GO:1900424 | regulation of defense response to bacterium |
Biological Process | GO:1901509 | regulation of endothelial tube morphogenesis |
Biological Process | GO:0010468 | regulation of gene expression |
Biological Process | GO:0050727 | regulation of inflammatory response |
Biological Process | GO:0032651 | regulation of interleukin-1 beta production |
Biological Process | GO:0032655 | regulation of interleukin-12 production |
Biological Process | GO:1901256 | regulation of macrophage colony-stimulating factor production |
Biological Process | GO:0045655 | regulation of monocyte differentiation |
Biological Process | GO:0006357 | regulation of transcription by RNA polymerase II |
Biological Process | GO:0032680 | regulation of tumor necrosis factor production |
Biological Process | GO:0032496 | response to lipopolysaccharide |
Biological Process | GO:0033574 | response to testosterone |
Biological Process | GO:0021756 | striatum development |
Molecular Function | GO:0000981 | DNA-binding transcription factor activity, RNA polymerase II-specific |
Molecular Function | GO:0001227 | DNA-binding transcription repressor activity, RNA polymerase II-specific |
Molecular Function | GO:0000978 | RNA polymerase II cis-regulatory region sequence-specific DNA binding |
Molecular Function | GO:0001046 | core promoter sequence-specific DNA binding |
Molecular Function | GO:0042802 | identical protein binding |
Molecular Function | GO:0046872 | metal ion binding |
Molecular Function | GO:0050681 | nuclear androgen receptor binding |
Molecular Function | GO:0043621 | protein self-association |
Molecular Function | GO:1990837 | sequence-specific double-stranded DNA binding |
Cellular Component | GO:0000785 | chromatin |
Cellular Component | GO:0005737 | cytoplasm |
Cellular Component | GO:0005654 | nucleoplasm |
Cellular Component | GO:0005634 | nucleus |
InterPro | InterPro name |
---|---|
IPR001766 | Fork head domain |
IPR030456 | Fork head domain conserved site 2 |
IPR032354 | FOXP, coiled-coil domain |
IPR036388 | Winged helix-like DNA-binding domain superfamily |
IPR036390 | Winged helix DNA-binding domain superfamily |
IPR047412 | Forkhead box protein P1/P2, forkhead domain |
Pfam | Pfam name |
---|---|
PF00250 | Forkhead domain |
PF16159 | FOXP coiled-coil domain |
Reactome | Reactome Name | Node type | Reactome Root | Reactome Root Name |
---|---|---|---|---|
R-HSA-452723 | Transcriptional regulation of pluripotent stem cells | Internal node | R-HSA-1266738 | Developmental Biology |
Location | ECO term | Pubmed |
---|---|---|
Nucleus | ECO:0000269 | PubMed:25027557 |
Nucleus | ECO:0000269 | PubMed:26647308 |
HPO ID | HPO name |
---|---|
HP:0000006 | Autosomal dominant inheritance |
HP:0000077 | Abnormality of the kidney |
HP:0000119 | Abnormality of the genitourinary system |
HP:0000194 | Open mouth |
HP:0000256 | Macrocephaly |
HP:0000272 | Malar flattening |
HP:0000278 | Retrognathia |
HP:0000303 | Mandibular prognathia |
HP:0000316 | Hypertelorism |
HP:0000403 | Recurrent otitis media |
HP:0000455 | Broad nasal tip |
HP:0000478 | Abnormality of the eye |
HP:0000486 | Strabismus |
HP:0000494 | Downslanted palpebral fissures |
HP:0000505 | Visual impairment |
HP:0000508 | Ptosis |
HP:0000539 | Abnormality of refraction |
HP:0000581 | Blepharophimosis |
HP:0000598 | Abnormality of the ear |
HP:0000614 | Abnormal nasolacrimal system morphology |
HP:0000639 | Nystagmus |
HP:0000708 | Atypical behavior |
HP:0000718 | Aggressive behavior |
HP:0000722 | Compulsive behaviors |
HP:0000729 | Autistic behavior |
HP:0000733 | Abnormal repetitive mannerisms |
HP:0000736 | Short attention span |
HP:0000739 | Anxiety |
HP:0000750 | Delayed speech and language development |
HP:0000805 | Enuresis |
HP:0000819 | Diabetes mellitus |
HP:0000820 | Abnormality of the thyroid gland |
HP:0000821 | Hypothyroidism |
HP:0000954 | Single transverse palmar crease |
HP:0000975 | Hyperhidrosis |
HP:0001212 | Prominent fingertip pads |
HP:0001249 | Intellectual disability |
HP:0001250 | Seizure |
HP:0001252 | Hypotonia |
HP:0001256 | Intellectual disability, mild |
HP:0001257 | Spasticity |
HP:0001263 | Global developmental delay |
HP:0001270 | Motor delay |
HP:0001290 | Generalized hypotonia |
HP:0001371 | Flexion contracture |
HP:0001508 | Failure to thrive |
HP:0001513 | Obesity |
HP:0001531 | Failure to thrive in infancy |
HP:0001581 | Recurrent skin infections |
HP:0001627 | Abnormal heart morphology |
HP:0001824 | Weight loss |
HP:0001903 | Anemia |
HP:0001945 | Fever |
HP:0002017 | Nausea and vomiting |
HP:0002019 | Constipation |
HP:0002027 | Abdominal pain |
HP:0002092 | Pulmonary arterial hypertension |
HP:0002113 | Pulmonary infiltrates |
HP:0002188 | Delayed CNS myelination |
HP:0002194 | Delayed gross motor development |
HP:0002205 | Recurrent respiratory infections |
HP:0002236 | Frontal upsweep of hair |
HP:0002307 | Drooling |
HP:0002342 | Intellectual disability, moderate |
HP:0002353 | EEG abnormality |
HP:0002463 | Language impairment |
HP:0002474 | Expressive language delay |
HP:0002714 | Downturned corners of mouth |
HP:0002716 | Lymphadenopathy |
HP:0002788 | Recurrent upper respiratory tract infections |
HP:0003196 | Short nose |
HP:0003593 | Infantile onset |
HP:0005272 | Prominent nasolabial fold |
HP:0007018 | Attention deficit hyperactivity disorder |
HP:0007301 | Oromotor apraxia |
HP:0008589 | Hypoplastic helices |
HP:0008762 | Repetitive compulsive behavior |
HP:0008872 | Feeding difficulties in infancy |
HP:0009088 | Speech articulation difficulties |
HP:0010864 | Intellectual disability, severe |
HP:0011098 | Speech apraxia |
HP:0011220 | Prominent forehead |
HP:0011298 | Prominent digit pad |
HP:0011823 | Chin with horizontal crease |
HP:0011968 | Feeding difficulties |
HP:0012123 | Posterior uveitis |
HP:0012191 | B-cell lymphoma |
HP:0012378 | Fatigue |
HP:0012393 | Allergy |
HP:0012471 | Thick vermilion border |
HP:0025502 | Overweight |
HP:0030084 | Clinodactyly |
HP:0031936 | Delayed ability to walk |
HP:0040303 | Decreased serum iron |
HP:0100716 | Self-injurious behavior |
HP:0100721 | Mediastinal lymphadenopathy |
HP:0410263 | Brain imaging abnormality |
Disease name | MONDO ID | ICD10 | ICD10 chapter | OMIM | Orphanet |
---|---|---|---|---|---|
strabismus | MONDO:0003432 | H50 | chapter7, Diseases of the eye and adnexa | ||
intellectual disability-severe speech delay-mild dysmorphism syndrome | MONDO:0013352 | Q87 | chapter17, Congenital malformations, deformations and chromosomal abnormalities | OMIM:613670 | Orphanet:391372 |