WormBase Tree Display for Gene: WBGene00018613

WBGene00018613 SMap: S_parent: Sequence: F48E8
  Identity: Version: 2
    Name: CGC_name: skpt-1 Person_evidence: WBPerson322
      Sequence_name: F48E8.7
      Molecular_name: F48E8.7a
        F48E8.7a.1
        CE28404
        F48E8.7b
        CE01959
        F48E8.7b.1
      Other_name: CELE_F48E8.7 Accession_evidence: NDB BX284603
      Public_name: skpt-1
    DB_info: Database: AceView gene 3G536
        WormQTL gene WBGene00018613
        WormFlux gene WBGene00018613
        NDB locus_tag CELE_F48E8.7
        Panther gene CAEEL|WormBase=WBGene00018613|UniProtKB=Q09397
          family PTHR16134
        NCBI gene 175749
        RefSeq protein NM_171865.7
            NM_171121.5
        TREEFAM TREEFAM_ID TF352582
        TrEMBL UniProtAcc Q8MQ34
            Q09397
        UniProt_GCRP UniProtAcc Q09397
    Species: Caenorhabditis elegans
    History: Version_change: 1 28 May 2004 13:31:00 WBPerson1971 Event: Imported: Initial conversion from CDS class of stlace from WS125
        2 02 Feb 2006 09:28:57 WBPerson2970 Name_change: CGC_name: skpt-1
    Status: Live
  Gene_info (9)
  Disease_info: Potential_model: DOID:0050866 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:10901)
      DOID:8991 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:10901)
      DOID:5409 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:10901)
      DOID:2671 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:10901)
      DOID:0080365 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:10901)
      DOID:10286 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:10901)
      DOID:4450 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:10901)
      DOID:10283 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:10901)
      DOID:1612 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:10901)
  Molecular_info: Corresponding_CDS: F48E8.7a
      F48E8.7b
    Corresponding_transcript: F48E8.7a.1
      F48E8.7b.1
    Other_sequence: CGC01410_1
      CBC05615_1
      CRC00200_1
      CR02293
      CJC16333_1
      CR10212
      CRC01355_1
    Associated_feature: WBsf651047
      WBsf651048
      WBsf976147
      WBsf976148
      WBsf976149
      WBsf226682
  Experimental_info: RNAi_result: WBRNAi00047756 Inferred_automatically: RNAi_primary
      WBRNAi00032491 Inferred_automatically: RNAi_primary
      WBRNAi00005292 Inferred_automatically: RNAi_primary
      WBRNAi00015255 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1023194
      Expr1038013
      Expr1151588
      Expr2015837
      Expr2034070
    Drives_construct: WBCnstr00026383
    Construct_product: WBCnstr00026383
    Microarray_results (25)
    Expression_cluster (182)
    Interaction (256)
  Map_info: Map: III Position: -1.69036 Error: 0.012144
    Positive: Positive_clone: F48E8 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference: WBPaper00012854
    WBPaper00028040
    WBPaper00028868
    WBPaper00038491
    WBPaper00055090
  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