WormBase Tree Display for Gene: WBGene00008711

WBGene00008711 SMap: S_parent: Sequence: F11E6
  Identity: Version: 1
    Name: Sequence_name: F11E6.8
      Molecular_name: F11E6.8a
        F11E6.8a.1
        CE19788
        F11E6.8b
        CE50655
        F11E6.8c
        CE45857
        F11E6.8b.1
        F11E6.8c.1
      Other_name: CELE_F11E6.8 Accession_evidence: NDB BX284604
      Public_name: F11E6.8
    DB_info: Database: AceView gene 4S388
        WormQTL gene WBGene00008711
        WormFlux gene WBGene00008711
        NDB locus_tag CELE_F11E6.8
        Panther gene CAEEL|WormBase=WBGene00008711|UniProtKB=Q9XVQ7
          family PTHR24416
        NCBI gene 178530
        RefSeq protein NM_001269033.3
            NM_001269031.4
            NM_001269032.3
        TrEMBL UniProtAcc F1LIN3
            C0P284
            Q9XVQ7
        UniProt_GCRP UniProtAcc Q9XVQ7
        OMIM gene 164860
            600168
    Species: Caenorhabditis elegans
    History: Version_change: 1 26 May 2004 16:54:49 WBPerson1971 Event: Imported: Initial conversion from CDS class of WS125
    Status: Live
  Gene_info: Biotype: SO:0001217
    Allele (207)
    Strain: WBStrain00032771
      WBStrain00037287
    RNASeq_FPKM (74)
    GO_annotation (16)
    Ortholog (58)
    Paralog (69)
    Structured_description: Automated_description: Predicted to enable transmembrane receptor protein tyrosine kinase activity. Predicted to be involved in cell migration; nervous system development; and transmembrane receptor protein tyrosine kinase signaling pathway. Predicted to be located in membrane. Predicted to be part of receptor complex. Human ortholog(s) of this gene implicated in several diseases, including autistic disorder; autosomal recessive nonsyndromic deafness 97; and carcinoma (multiple). Is an ortholog of human MET (MET proto-oncogene, receptor tyrosine kinase) and MST1R (macrophage stimulating 1 receptor). Paper_evidence: WBPaper00065943
          Curator_confirmed: WBPerson324
            WBPerson37462
          Inferred_automatically: This description was generated automatically by a script based on data from the WS291 version of WormBase
          Date_last_updated: 29 Nov 2023 00:00:00
  Disease_info: Potential_model: DOID:4552 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7029)
      DOID:12849 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7029)
      DOID:1115 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7029)
      DOID:2349 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7029)
      DOID:0050865 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7029)
      DOID:9538 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7029)
      DOID:5577 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7029)
      DOID:0050866 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7029)
      DOID:4947 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7029)
      DOID:3008 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7029)
      DOID:3908 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7029)
      DOID:4465 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7029)
      DOID:0050646 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7029)
      DOID:2394 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7029)
      DOID:10286 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7029)
      DOID:4450 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7029)
      DOID:9261 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7381)
      DOID:3587 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7029)
      DOID:1793 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7029)
      DOID:684 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7029)
      DOID:0110539 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7029)
  Molecular_info: Corresponding_CDS: F11E6.8a
      F11E6.8b
      F11E6.8c
    Corresponding_CDS_history: F11E6.8b:wp247
    Corresponding_transcript: F11E6.8a.1
      F11E6.8b.1
      F11E6.8c.1
    Other_sequence (19)
    Associated_feature: WBsf668591
      WBsf668592
      WBsf668593
      WBsf668594
      WBsf668595
      WBsf717216
      WBsf718265
      WBsf718266
      WBsf718267
      WBsf999040
  Experimental_info: RNAi_result (3)
    Expr_pattern: Expr1017952
      Expr1033794
      Expr1148344
      Expr2002458
      Expr2020674
    Drives_construct: WBCnstr00032753
    Construct_product: WBCnstr00032753
    Microarray_results (21)
    Expression_cluster (197)
    Interaction (25)
  Map_info: Positive: Positive_clone: F11E6 Inferred_automatically: From sequence, transcript, pseudogene data
    Interpolated_map_position: IV 17.0456
  Reference: WBPaper00027258
    WBPaper00038491
    WBPaper00055090
  Method: Gene