ENSG00000073861


Homo sapiens

Features
Gene ID: ENSG00000073861
  
Biological name :TBX21
  
Synonyms : Q9UL17 / T-box 21 / TBX21
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 17
Strand: 1
Band: q21.32
Gene start: 47733244
Gene end: 47746119
  
Corresponding Affymetrix probe sets: 220684_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000177694
NCBI entrez gene - 30009     See in Manteia.
OMIM - 604895
RefSeq - NM_013351
RefSeq - XM_011524698
RefSeq Peptide - NP_037483
swissprot - Q9UL17
Ensembl - ENSG00000073861
  
Related genetic diseases (OMIM): 208550 - Asthma and nasal polyps, 208550

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
 tbx21ENSDARG00000004473Danio rerio
 Tbx21ENSMUSG00000001444Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
EOMES / O95936 / eomesoderminENSG0000016350844
TBR1 / Q16650 / T-box, brain 1ENSG0000013653541
TBXT / O15178 / T-box transcription factor TENSG0000016445825
MGA / Q8IWI9 / MGA, MAX dimerization proteinENSG0000017419725
TBX19 / O60806 / T-box 19ENSG0000014317823


Protein motifs (from Interpro)
Interpro ID Name
 IPR001699  Transcription factor, T-box
 IPR008967  p53-like transcription factor, DNA-binding
 IPR018186  Transcription factor, T-box, conserved site
 IPR036960  T-box superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0000122 negative regulation of transcription by RNA polymerase II IDA
 biological_processGO:0006351 transcription, DNA-templated IEA
 biological_processGO:0006355 regulation of transcription, DNA-templated TAS
 biological_processGO:0007275 multicellular organism development TAS
 biological_processGO:0009615 response to virus IEP
 biological_processGO:0030217 T cell differentiation IEA
 biological_processGO:0032703 negative regulation of interleukin-2 production IEA
 biological_processGO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process IEA
 biological_processGO:0045580 regulation of T cell differentiation IEA
 biological_processGO:0045892 negative regulation of transcription, DNA-templated IEA
 biological_processGO:0045893 positive regulation of transcription, DNA-templated IEA
 biological_processGO:0048304 positive regulation of isotype switching to IgG isotypes IEA
 biological_processGO:0050776 regulation of immune response IEA
 biological_processGO:0071310 cellular response to organic substance IEA
 biological_processGO:0072676 lymphocyte migration IEA
 biological_processGO:2000320 negative regulation of T-helper 17 cell differentiation IEA
 biological_processGO:2000329 negative regulation of T-helper 17 cell lineage commitment IEA
 biological_processGO:2000552 negative regulation of T-helper 2 cell cytokine production IEA
 cellular_componentGO:0005634 nucleus ISS
 cellular_componentGO:0043025 neuronal cell body IEA
 molecular_functionGO:0000981 RNA polymerase II transcription factor activity, sequence-specific DNA binding NAS
 molecular_functionGO:0001227 transcriptional repressor activity, RNA polymerase II transcription regulatory region sequence-specific DNA binding IC
 molecular_functionGO:0003677 DNA binding IEA
 molecular_functionGO:0003700 DNA-binding transcription factor activity TAS
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0043565 sequence-specific DNA binding IDA
 molecular_functionGO:0044212 transcription regulatory region DNA binding IDA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000007 Autosomal recessive 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 homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators]
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 HP:0002099 Asthma "Asthma is characterized by increased responsiveness of the tracheobronchial tree to multiple stimuli, leading to narrowing of the air passages with resultant dyspnea, cough, and wheezing." [HPO:curators]
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 HP:0012042 Aspirin-induced asthma "A type of asthma in which aspirin and other nonsteroidal anti-inflammatory drugs (NSAIDs) that inhibit cyclooxygen-ase 1 (COX-1) exacerbate bronchoconstriction." [pmid:12743549]
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 HP:0100582 Nasal polyposis "Polypoidal masses arising mainly from the mucous membranes of the nose and paranasal sinuses. They are freely movable and nontender overgrowths of the mucosa that frequently accompany allergic rhinitis." [HPO:sdoelken]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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