ENSG00000145022


Homo sapiens

Features
Gene ID: ENSG00000145022
  
Biological name :TCTA
  
Synonyms : P57738 / T cell leukemia translocation altered / TCTA
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 3
Strand: 1
Band: p21.31
Gene start: 49412206
Gene end: 49416475
  
Corresponding Affymetrix probe sets: 203054_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000273590
NCBI entrez gene - 6988     See in Manteia.
OMIM - 600690
RefSeq - NM_022171
RefSeq Peptide - NP_071503
swissprot - P57738
Ensembl - ENSG00000145022
  
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
 tctaENSDARG00000044194Danio rerio
 TctaENSMUSG00000039461Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
No match


Protein motifs (from Interpro)
Interpro ID Name
 IPR016560  T-cell leukemia translocation-altered gene protein


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0045671 negative regulation of osteoclast differentiation IDA
 biological_processGO:0072675 osteoclast fusion IDA
 cellular_componentGO:0005622 intracellular IDA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 molecular_functionGO:0003674 molecular_function ND


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
No match
  


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






 

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contact: otassy@igbmc.fr