ENSG00000125850


Homo sapiens

Features
Gene ID: ENSG00000125850
  
Biological name :OVOL2
  
Synonyms : OVOL2 / ovo like zinc finger 2 / Q9BRP0
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 20
Strand: -1
Band: p11.23
Gene start: 17956979
Gene end: 18059188
  
Corresponding Affymetrix probe sets: 206048_at (Human Genome U133 Plus 2.0 Array)   211778_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000278780
NCBI entrez gene - 58495     See in Manteia.
OMIM - 616441
RefSeq - NM_021220
RefSeq Peptide - NP_067043
swissprot - Q9BRP0
Ensembl - ENSG00000125850
  
Related genetic diseases (OMIM): 122000 - Corneal dystrophy, posterior polymorphous, 1, 122000

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
 OVOL2ENSGALG00000008702Gallus gallus
 Ovol2ENSMUSG00000037279Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
OVOL1 / O14753 / ovo like transcriptional repressor 1ENSG0000017281851
OVOL3 / O00110 / ovo like zinc finger 3ENSG0000010526135
Q6ZSB9 / ZBTB49 / zinc finger and BTB domain containing 49ENSG0000016882622
MYNN / Q9NPC7 / myoneurinENSG0000008527422


Protein motifs (from Interpro)
Interpro ID Name
 IPR013087  Zinc finger C2H2-type
 IPR027756  Ovo-like
 IPR036236  Zinc finger C2H2 superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001525 angiogenesis IEA
 biological_processGO:0001755 neural crest cell migration IEA
 biological_processGO:0001842 neural fold formation IEA
 biological_processGO:0001947 heart looping IEA
 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:0006366 transcription by RNA polymerase II IEA
 biological_processGO:0007275 multicellular organism development IEA
 biological_processGO:0007507 heart development IEA
 biological_processGO:0008285 negative regulation of cell proliferation IEA
 biological_processGO:0008544 epidermis development IEA
 biological_processGO:0009913 epidermal cell differentiation IEA
 biological_processGO:0009953 dorsal/ventral pattern formation IEA
 biological_processGO:0010719 negative regulation of epithelial to mesenchymal transition IEA
 biological_processGO:0010837 regulation of keratinocyte proliferation IEA
 biological_processGO:0045618 positive regulation of keratinocyte differentiation IEA
 biological_processGO:0045892 negative regulation of transcription, DNA-templated IEA
 biological_processGO:0045893 positive regulation of transcription, DNA-templated IEA
 biological_processGO:0045944 positive regulation of transcription by RNA polymerase II IEA
 biological_processGO:0048557 embryonic digestive tract morphogenesis IEA
 biological_processGO:0060214 endocardium formation IEA
 biological_processGO:0060347 heart trabecula formation IEA
 biological_processGO:0060716 labyrinthine layer blood vessel development IEA
 biological_processGO:2000647 negative regulation of stem cell proliferation IEA
 cellular_componentGO:0005634 nucleus IBA
 molecular_functionGO:0000981 RNA polymerase II transcription factor activity, sequence-specific DNA binding IBA
 molecular_functionGO:0001228 transcriptional activator activity, RNA polymerase II transcription regulatory region sequence-specific DNA binding IEA
 molecular_functionGO:0003676 nucleic acid binding IEA
 molecular_functionGO:0003677 DNA binding IEA
 molecular_functionGO:0003682 chromatin binding IEA
 molecular_functionGO:0046872 metal ion binding IEA


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]
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 HP:0000501 Glaucoma "Glaucoma refers loss of retinal ganglion cells in a characteristic pattern of optic neuropathy usually associated with increased intraocular pressure." [HPO:curators]
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 HP:0000585 Band keratopathy "An `abnormality of the cornea` (HP:0000481) characterized by the deposition of calcium in a band across the central cornea, leading to decreased vision, foreign body sensation, and ocular irritation." [HPO:probinson]
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 HP:0000613 Photophobia "Excessive sensitivity to light with the sensation of discomfort or pain in the eyes due to exposure to bright light." [HPO:curators]
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 HP:0001089 Iris atrophy 
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 HP:0007915 Polymorphous posterior corneal dystrophy "This corneal dystrophy affects the posterior limiting membrane of the cornea and is characterized by polymorphous plaques of calcium deposits in the deep stromal layers of the cornea, and occasionally by vesicular lesions of the endothelium and edema of the deep corneal stroma." [HPO:curators]
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 HP:0009918 Ectopia pupillae "A malposition of the pupil." [HPO:curators]
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 HP:0009926 Increased tear production "Abnormally in creased lacrimation." [HPO:curators]
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 HP:0011483 Anterior synechiae of the anterior chamber "Adhesions between the iris and the cornea." [DDD:ncarter]
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 HP:0025358 Uveal ectropion "Presence of iris pigment epithelium on the anterior surface of the iris." []
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 HP:0031159 Thinning of Descemet membrane "A reduction in the thickness of Descemet s membrane." []
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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