ENSG00000183770


Homo sapiens

Features
Gene ID: ENSG00000183770
  
Biological name :FOXL2
  
Synonyms : forkhead box L2 / FOXL2 / P58012
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 3
Strand: -1
Band: q22.3
Gene start: 138944224
Gene end: 138947140
  
Corresponding Affymetrix probe sets: 220102_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000333188
NCBI entrez gene - 668     See in Manteia.
OMIM - 605597
RefSeq - NM_023067
RefSeq Peptide - NP_075555
swissprot - P58012
swissprot - Q53ZD3
Ensembl - ENSG00000183770
  
Related genetic diseases (OMIM): 110100 - Blepharophimosis, epicanthus inversus, and ptosis, type 1, 110100
  608996 - Premature ovarian failure 3, 608996

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
 foxl2aENSDARG00000042180Danio rerio
 foxl2bENSDARG00000068417Danio rerio
 FOXL2ENSGALG00000029282Gallus gallus
 Foxl2ENSMUSG00000050397Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
FOXC2 / Q99958 / forkhead box C2ENSG0000017669229
FOXC1 / Q12948 / forkhead box C1ENSG0000005459829
FOXS1 / O43638 / forkhead box S1ENSG0000017977227
FOXL1 / Q12952 / forkhead box L1ENSG0000017667825
FOXI1 / Q12951 / forkhead box I1ENSG0000016826923
FOXI3 / A8MTJ6 / forkhead box I3ENSG0000021433622
FOXB1 / Q99853 / forkhead box B1ENSG0000017195622
FOXI2 / Q6ZQN5 / forkhead box I2ENSG0000018676622
FOXB2 / Q5VYV0 / forkhead box B2ENSG0000020461221
FOXA1 / P55317 / forkhead box A1ENSG0000012951421
FOXA2 / Q9Y261 / forkhead box A2ENSG0000012579821
FOXA3 / P55318 / forkhead box A3ENSG0000017060818


Protein motifs (from Interpro)
Interpro ID Name
 IPR001766  Fork head domain
 IPR018122  Fork head domain conserved site1
 IPR030456  Fork head domain conserved site 2
 IPR036388  Winged helix-like DNA-binding domain superfamily
 IPR036390  Winged helix DNA-binding domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0000122 negative regulation of transcription by RNA polymerase II IEA
 biological_processGO:0001541 ovarian follicle development IEA
 biological_processGO:0001555 oocyte growth IEA
 biological_processGO:0002074 extraocular skeletal muscle development IMP
 biological_processGO:0006309 apoptotic DNA fragmentation IMP
 biological_processGO:0006351 transcription, DNA-templated IEA
 biological_processGO:0006355 regulation of transcription, DNA-templated IEA
 biological_processGO:0006366 transcription by RNA polymerase II IEA
 biological_processGO:0007338 single fertilization IEA
 biological_processGO:0008585 female gonad development IEA
 biological_processGO:0009653 anatomical structure morphogenesis IBA
 biological_processGO:0019101 female somatic sex determination IEA
 biological_processGO:0030154 cell differentiation IBA
 biological_processGO:0033686 positive regulation of luteinizing hormone secretion IEA
 biological_processGO:0043065 positive regulation of apoptotic process IGI
 biological_processGO:0043280 positive regulation of cysteine-type endopeptidase activity involved in apoptotic process IMP
 biological_processGO:0045892 negative regulation of transcription, DNA-templated IEA
 biological_processGO:0045893 positive regulation of transcription, DNA-templated ISS
 biological_processGO:0045944 positive regulation of transcription by RNA polymerase II IEA
 biological_processGO:0046881 positive regulation of follicle-stimulating hormone secretion IEA
 biological_processGO:0048048 embryonic eye morphogenesis IEA
 biological_processGO:0060014 granulosa cell differentiation IEA
 biological_processGO:0060065 uterus development IEA
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005654 nucleoplasm TAS
 cellular_componentGO:0045171 intercellular bridge IDA
 molecular_functionGO:0000978 RNA polymerase II proximal promoter sequence-specific DNA binding IEA
 molecular_functionGO:0000981 RNA polymerase II transcription factor activity, sequence-specific DNA binding IBA
 molecular_functionGO:0001077 transcriptional activator activity, RNA polymerase II proximal promoter sequence-specific DNA binding IEA
 molecular_functionGO:0003677 DNA binding TAS
 molecular_functionGO:0003700 DNA-binding transcription factor activity NAS
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0030331 estrogen receptor binding IEA
 molecular_functionGO:0031624 ubiquitin conjugating enzyme binding IPI
 molecular_functionGO:0043028 cysteine-type endopeptidase regulator activity involved in apoptotic process IMP
 molecular_functionGO:0043565 sequence-specific DNA binding IEA


Pathways (from Reactome)
Pathway description
SUMOylation of transcription factors


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]
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 HP:0000013 Hypoplastic uterus 
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 HP:0000141 Amenorrhea 
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 HP:0000218 High palate "Height of the palate more than 2 SD above the mean (objective) or palatal height at the level of the first permanent molar more than twice the height of the teeth (subjective)." [pmid:19125428]
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 HP:0000378 Cup-shaped ears "Small auricles that grow forward over the meatus (ear canal)." [HPO:curators]
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 HP:0000431 Broad nasal bridge "Increased horizontal dimension of the upper, bony part of the nose." [HPO:curators]
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 HP:0000482 Microcornea "A congenital abnormality of the `cornea` (FMA:58238) in which the cornea and the anterior segment of the eye are smaller than normal. The horizontal diameter of the cornea does not reach 10 mm even in adulthood." [HPO:probinson]
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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:0000506 Telecanthus "An abnormally increased distance between the medial canthi (angle between eyelids) of the eyelids." [HPO:curators]
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 HP:0000508 Ptosis "Drooping of the eyelid." [HPO:curators]
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 HP:0000537 Epicanthus inversus 
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 HP:0000540 Hypermetropia 
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 HP:0000568 Microphthalmos "A developmental anomaly characterized by abnormal smallness of one or both eyes." [HPO:curators]
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 HP:0000581 Blepharophimosis "Reduced width of the palpebral fissures." [HPO:sdoelken]
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 HP:0000639 Nystagmus "Rhythmic, involuntary oscillations of one or both eyes related to abnormality in fixation, conjugate gaze, or vestibular mechanisms." [HPO:curators]
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 HP:0000769 Abnormality of the breasts 
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 HP:0000837 Elevated gonadotropins 
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 HP:0000869 Secondary amenorrhea 
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 HP:0001595 Hair abnormality 
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 HP:0005280 Depressed nasal root and bridge 
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 HP:0008209 Premature ovarian failure 
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 HP:0008222 Female infertility 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000116030 SUMO1 / P63165 / small ubiquitin-like modifier 1  / reaction / complex
 ENSG00000103275 UBE2I / P63279 / ubiquitin conjugating enzyme E2 I  / reaction






 

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