WormBase Tree Display for Gene: WBGene00022774

WBGene00022774 SMap: S_parent: Sequence: ZK616
  Identity: Version: 2
    Name: CGC_name: swsn-6 Person_evidence: WBPerson552
            WBPerson407
      Sequence_name: ZK616.4
      Molecular_name: ZK616.4
        ZK616.4.1
        CE31753
      Other_name: psa-13
        ZK616.g Curator_confirmed: WBPerson1983
          Remark: Old cosmid naming mapped via unique overlapping PCR_product on CDSs
        CELE_ZK616.4 Accession_evidence: NDB BX284604
      Public_name: swsn-6
    DB_info: Database (12)
    Species: Caenorhabditis elegans
    History: Version_change: 1 28 May 2004 13:31:06 WBPerson1971 Event: Imported: Initial conversion from CDS class of stlace from WS125
        2 11 Feb 2011 15:20:38 WBPerson2970 Name_change: CGC_name: swsn-6
                Other_name: psa-13
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: swsn
    Allele (21)
    Strain: WBStrain00037038
    RNASeq_FPKM (74)
    GO_annotation: 00094790
      00094791
      00094792
      00094793
      00094794
      00094795
      00094796
    Ortholog (51)
    Paralog (11)
    Structured_description: Automated_description: Predicted to enable chromatin binding activity. Predicted to be involved in nervous system development and regulation of transcription by RNA polymerase II. Predicted to be part of NuA4 histone acetyltransferase complex and SWI/SNF complex. Used to study alcohol use disorder. Human ortholog(s) of this gene implicated in developmental and epileptic encephalopathy 76. Is an ortholog of human ACTL6B (actin like 6B). 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: Experimental_model: DOID:1574 Homo sapiens Paper_evidence: WBPaper00046494
          Curator_confirmed: WBPerson324
          Date_last_updated: 20 May 2019 00:00:00
    Potential_model: DOID:0112212 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:160)
  Models_disease_in_annotation: WBDOannot00000667
  Molecular_info: Corresponding_CDS: ZK616.4
    Corresponding_CDS_history: ZK616.4:wp83
    Corresponding_transcript: ZK616.4.1
    Other_sequence (39)
    Associated_feature: WBsf645971
      WBsf659829
      WBsf228302
      WBsf228303
  Experimental_info: RNAi_result: WBRNAi00116273 Inferred_automatically: RNAi_primary
      WBRNAi00059551 Inferred_automatically: RNAi_primary
      WBRNAi00116272 Inferred_automatically: RNAi_primary
      WBRNAi00059550 Inferred_automatically: RNAi_primary
      WBRNAi00061244 Inferred_automatically: RNAi_primary
      WBRNAi00080507 Inferred_automatically: RNAi_primary
      WBRNAi00061245 Inferred_automatically: RNAi_primary
    Expr_pattern: Expr1024374
      Expr1040069
      Expr1162967
      Expr2017160
      Expr2035296
    Drives_construct: WBCnstr00023985
    Construct_product: WBCnstr00023985
    Microarray_results (18)
    Expression_cluster (117)
    Interaction (78)
  Map_info: Map: IV Position: 1.65458 Error: 0.001601
    Positive: Positive_clone: ZK616 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference: WBPaper00024200
    WBPaper00038491
    WBPaper00046494
    WBPaper00048193
    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