WormBase Tree Display for Gene: WBGene00006543

WBGene00006543 SMap: S_parent: Sequence: F21H11
  Identity: Version: 2
    Name: CGC_name: tbx-2 Person_evidence: WBPerson107
      Sequence_name: F21H11.3
      Molecular_name: F21H11.3
        F21H11.3.1
        CE01245
      Other_name: sdf-13
        mab-22 Person_evidence: WBPerson261
        CELE_F21H11.3 Accession_evidence: NDB BX284603
      Public_name: tbx-2
    DB_info: Database: AceView gene 3G222
        WormQTL gene WBGene00006543
        WormFlux gene WBGene00006543
        NDB locus_tag CELE_F21H11.3
        Panther gene CAEEL|WormBase=WBGene00006543|UniProtKB=Q19691
          family PTHR11267
        NCBI gene 175698
        RefSeq protein NM_001382860.2
        SwissProt UniProtAcc Q19691
        UniProt_GCRP UniProtAcc Q19691
        OMIM gene 600747
            601621
    Species: Caenorhabditis elegans
    History: Version_change: 1 07 Apr 2004 11:29:40 WBPerson1971 Event: Imported: Initial conversion from geneace
        2 31 Jul 2013 13:40:41 WBPerson2970 Event: Acquires_merge: WBGene00003113
              Name_change: Other_name: mab-22
      Acquires_merge: WBGene00003113
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: tbx
    Allele (60)
    Legacy_information: [C.elegansII] NMK. Similarity to mouse Tbx genes, closest to mouse Tbx2 (70% identity in T box domain). (F21H11.3)[Agulnik et al. 1995]
      [C.elegansII] bx59ts : extensive loss of rays at 25C, not 15C. Divisions appear normal, possible ray assembly defect. NA1. [EM]
    Strain: WBStrain00003711
      WBStrain00022191
      WBStrain00022192
      WBStrain00035675
      WBStrain00007174
      WBStrain00049269
    RNASeq_FPKM (74)
    GO_annotation (35)
    Ortholog (42)
    Paralog (21)
    Structured_description (2)
  Disease_info: Potential_model: DOID:9256 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:11602)
      DOID:0060614 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:11602)
      DOID:10534 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:11602)
      DOID:1882 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:11597)
      DOID:1681 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:11597)
      DOID:2394 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:11602)
      DOID:0070345 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:11597)
      DOID:684 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:11602)
  Molecular_info: Corresponding_CDS: F21H11.3
    Corresponding_transcript: F21H11.3.1
    Other_sequence (16)
    Associated_feature (13)
    Gene_product_binds: WBsf977981
      WBsf977982
      WBsf977983
    Transcription_factor: WBTranscriptionFactor000208
  Experimental_info: RNAi_result (16)
    Expr_pattern (16)
    Drives_construct (12)
    Construct_product: WBCnstr00011882
      WBCnstr00011883
      WBCnstr00034310
    Regulate_expr_cluster: WBPaper00042274:tbx-2(bx59)_downregulated
      WBPaper00042274:tbx-2(bx59)_upregulated
    Antibody: WBAntibody00000713
    Microarray_results (19)
    Expression_cluster (199)
    Interaction (62)
    Anatomy_function: WBbtf0263
      WBbtf0264
  Map_info: Map: III Position: -2.08974 Error: 0.015753
    Positive: Positive_clone: F21H11 Inferred_automatically: From sequence, transcript, pseudogene data
    Mapping_data: Multi_point: 4725
    Pseudo_map_position
  Reference (58)
  Remark: Map position created from combination of previous interpolated map position (based on known location of sequence) and allele information. Therefore this is not a genetic map position based on recombination frequencies or genetic experiments. This was done on advice of the CGC. CGC_data_submission
  Method: Gene