ENSG00000114861


Homo sapiens

Features
Gene ID: ENSG00000114861
  
Biological name :FOXP1
  
Synonyms : forkhead box P1 / FOXP1 / Q9H334
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 3
Strand: -1
Band: p13
Gene start: 70952817
Gene end: 71583993
  
Corresponding Affymetrix probe sets: 1558996_at (Human Genome U133 Plus 2.0 Array)   223287_s_at (Human Genome U133 Plus 2.0 Array)   223936_s_at (Human Genome U133 Plus 2.0 Array)   223937_at (Human Genome U133 Plus 2.0 Array)   224837_at (Human Genome U133 Plus 2.0 Array)   224838_at (Human Genome U133 Plus 2.0 Array)   229844_at (Human Genome U133 Plus 2.0 Array)   235444_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000418784
Ensembl peptide - ENSP00000418524
Ensembl peptide - ENSP00000418883
Ensembl peptide - ENSP00000484963
Ensembl peptide - ENSP00000484803
Ensembl peptide - ENSP00000482847
Ensembl peptide - ENSP00000479663
Ensembl peptide - ENSP00000477918
Ensembl peptide - ENSP00000420736
Ensembl peptide - ENSP00000419393
Ensembl peptide - ENSP00000318721
Ensembl peptide - ENSP00000318902
Ensembl peptide - ENSP00000333560
Ensembl peptide - ENSP00000417857
Ensembl peptide - ENSP00000417941
Ensembl peptide - ENSP00000418102
Ensembl peptide - ENSP00000418225
NCBI entrez gene - 27086     See in Manteia.
OMIM - 605515
RefSeq - XM_017006168
RefSeq - NM_001012505
RefSeq - NM_001244808
RefSeq - NM_001244810
RefSeq - NM_001244812
RefSeq - NM_001244813
RefSeq - NM_001244814
RefSeq - NM_001244815
RefSeq - NM_001244816
RefSeq - NM_001349344
RefSeq - NM_032682
RefSeq - XM_005264735
RefSeq - XM_005264736
RefSeq - XM_005264737
RefSeq - XM_005264742
RefSeq - XM_006713102
RefSeq - XM_006713103
RefSeq - XM_006713104
RefSeq - XM_011533584
RefSeq - XM_011533585
RefSeq - XM_011533588
RefSeq - XM_017006165
RefSeq - XM_017006166
RefSeq - XM_017006167
RefSeq Peptide - NP_001231741
RefSeq Peptide - NP_001231743
RefSeq Peptide - NP_001231744
RefSeq Peptide - NP_001231745
RefSeq Peptide - NP_001336267
RefSeq Peptide - NP_001336268
RefSeq Peptide - NP_001336269
RefSeq Peptide - NP_001336271
RefSeq Peptide - NP_001336273
RefSeq Peptide - NP_116071
RefSeq Peptide - NP_001012523
RefSeq Peptide - NP_001231737
RefSeq Peptide - NP_001231739
RefSeq Peptide - NP_001231742
swissprot - Q9H334
swissprot - E9PFD3
swissprot - C9J5T4
swissprot - C9J0F0
swissprot - C9IYY1
swissprot - A0A0B4J2F3
swissprot - A0A087X2G3
swissprot - A0A087X299
swissprot - G5E965
swissprot - H0Y882
swissprot - A0A087WVT2
swissprot - Q548T7
Ensembl - ENSG00000114861
  
Related genetic diseases (OMIM): 613670 - Mental retardation with language impairment and with or without autistic features, 613670

This gene has been taged as a transcription factor by TFT
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
No match


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
FOXP2 / O15409 / forkhead box P2ENSG0000012857364
FOXP4 / Q8IVH2 / forkhead box P4ENSG0000013716656
FOXP3 / Q9BZS1 / forkhead box P3ENSG0000004976823
FOXD2 / O60548 / forkhead box D2ENSG0000018656410
FOXG1 / P55316 / forkhead box G1ENSG0000017616510
FOXF2 / Q12947 / forkhead box F2ENSG000001372739
FOXD3 / Q9UJU5 / forkhead box D3ENSG000001871409
FOXE1 / O00358 / forkhead box E1ENSG000001789199
FOXE3 / Q13461 / forkhead box E3ENSG000001867909
FOXD1 / Q16676 / forkhead box D1ENSG000002514939
FOXD4 / Q12950 / forkhead box D4ENSG000001701228
AC187653.1ENSG000002487678
Q9NU39 / FOXD4L1 / forkhead box D4 like 1ENSG000001844928
Q3SYB3 / FOXD4L6 / forkhead box D4 like 6ENSG000002735148
Q6VB84 / FOXD4L3 / forkhead box D4 like 3ENSG000001875598
FOXQ1 / Q9C009 / forkhead box Q1ENSG000001643798
FOXF1 / Q12946 / forkhead box F1ENSG000001032418
Q5VV16 / FOXD4L5 / forkhead box D4 like 5ENSG000002047798
Q8WXT5 / FOXD4L4 / forkhead box D4 like 4ENSG000001846598
FOXH1 / O75593 / forkhead box H1ENSG000001609737


Protein motifs (from Interpro)
Interpro ID 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


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0002903 negative regulation of B cell apoptotic process IDA
 biological_processGO:0006351 transcription, DNA-templated IEA
 biological_processGO:0006355 regulation of transcription, DNA-templated IEA
 biological_processGO:0006357 regulation of transcription by RNA polymerase II IEA
 biological_processGO:0010595 positive regulation of endothelial cell migration IMP
 biological_processGO:0030316 osteoclast differentiation IDA
 biological_processGO:0032496 response to lipopolysaccharide IDA
 biological_processGO:0032680 regulation of tumor necrosis factor production IDA
 biological_processGO:0035019 somatic stem cell population maintenance TAS
 biological_processGO:0035926 chemokine (C-C motif) ligand 2 secretion IDA
 biological_processGO:0036035 osteoclast development IDA
 biological_processGO:0042116 macrophage activation IDA
 biological_processGO:0042117 monocyte activation IDA
 biological_processGO:0042118 endothelial cell activation IMP
 biological_processGO:0045655 regulation of monocyte differentiation IDA
 biological_processGO:0045892 negative regulation of transcription, DNA-templated IMP
 biological_processGO:0048661 positive regulation of smooth muscle cell proliferation IMP
 biological_processGO:0050706 regulation of interleukin-1 beta secretion IDA
 biological_processGO:0050727 regulation of inflammatory response IDA
 biological_processGO:0060766 negative regulation of androgen receptor signaling pathway IDA
 biological_processGO:0061470 T follicular helper cell differentiation ISS
 biological_processGO:0072619 interleukin-21 secretion ISS
 biological_processGO:1900424 regulation of defense response to bacterium IDA
 biological_processGO:1901256 regulation of macrophage colony-stimulating factor production IDA
 biological_processGO:1901509 regulation of endothelial tube morphogenesis IMP
 biological_processGO:2001182 regulation of interleukin-12 secretion IDA
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005654 nucleoplasm IDA
 molecular_functionGO:0000981 RNA polymerase II transcription factor activity, sequence-specific DNA binding IBA
 molecular_functionGO:0003677 DNA binding IEA
 molecular_functionGO:0003700 DNA-binding transcription factor activity IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0042802 identical protein binding IPI
 molecular_functionGO:0043565 sequence-specific DNA binding IEA
 molecular_functionGO:0043621 protein self-association IMP
 molecular_functionGO:0046872 metal ion binding IEA
 molecular_functionGO:0050681 androgen receptor binding IDA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000006 Autosomal dominant inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele." [HPO:curators]
Show

 HP:0000194 Open mouth 
Show

 HP:0000256 Macrocephaly "The presence of an abnormally large `skull` (FMA:46565)." [HPO:probinson]
Show

 HP:0000278 Retrognathia 
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 HP:0000316 Hypertelorism 
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 HP:0000455 Broad nasal tip 
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 HP:0000486 Strabismus "Strabismus (also known as squint) is a condition in which the eyes are not properly aligned with each other." [HPO:curators]
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 HP:0000494 Downward slanting palpebral fissures 
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 HP:0000505 Impaired vision 
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 HP:0000614 Abnormality of the lacrimal duct 
Show

 HP:0000639 Nystagmus "Rhythmic, involuntary oscillations of one or both eyes related to abnormality in fixation, conjugate gaze, or vestibular mechanisms." [HPO:curators]
Show

 HP:0000718 Aggressive behavior "Aggressive behavior can denote verbal aggression, physical aggression against objects, physical aggression against people, and may also include aggression towards oneself." [HPO:curators]
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 HP:0000733 Stereotyped, repetitive behaviour 
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 HP:0000750 Impaired language development 
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 HP:0000752 Hyperactivity 
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 HP:0000820 Abnormality of the thyroid gland 
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 HP:0000975 Hyperhidrosis "An abnormally increased perspiration." [HPO:probinson]
Show

 HP:0001249 Mental retardation 
Show

 HP:0001290 Generalized hypotonia "Generalized muscular hypotonia (abnormally low muscle tone)." [HPO:curators]
Show

 HP:0001513 Obesity "A status with BODY WEIGHT that is grossly above the acceptable or desirable weight, usually due to accumulation of excess FATS in the body. The standards may vary with age, sex, genetic or cultural background. In the BODY MASS INDEX, a BMI greater than 30.0 kg/m2 is considered obese, and a BMI greater than 40.0 kg/m2 is considered morbidly obese (MORBID OBESITY)." [MeSH:D009765]
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 HP:0001824 Weight loss 
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 HP:0001903 Anemia 
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 HP:0001945 Fever 
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 HP:0002017 Nausea and vomiting 
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 HP:0002019 Constipation 
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 HP:0002027 Abdominal pain 
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 HP:0002113 Pulmonary infiltrates 
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 HP:0002194 Delayed gross motor development 
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 HP:0002205 Recurrent respiratory infections 
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 HP:0003196 Nasal hypoplasia "Underdevelopment of the `nose` (FMA:46472)." [HPO:probinson]
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 HP:0011220 Prominent forehead "Forward prominence of the entire forehead, due to protrusion of the frontal bone." [pmid:19125436]
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 HP:0012123 Posterior uveitis "Inflammation of the uveal tract in which the primary site of inflammation is the retina or choroid." [HPO:probinson]
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 HP:0012191 B-cell lymphoma "A type of lymphoma that originates in B-cells." [HPO:probinson]
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 HP:0012378 Fatigue "A subjective feeling of tiredness characterized by a lack of energy and motivation." [HPO:probinson]
Show

 HP:0012448 Delayed myelination "`Delayed` (PATO:0000502) `myelination` (GO:0042552)." [ORCID:0000-0001-5208-3432]
Show

 HP:0100721 Mediastinal lymphadenopathy 
Show

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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