WormBase Tree Display for Gene: WBGene00008218

WBGene00008218 SMap: S_parent: Sequence: C50B6
  Identity: Version: 2
    Name: CGC_name: nasp-2 Person_evidence: WBPerson117
      Sequence_name: C50B6.2
      Molecular_name: C50B6.2
        C50B6.2.1
        CE08871
      Other_name: CELE_C50B6.2 Accession_evidence: NDB BX284605
      Public_name: nasp-2
    DB_info: Database: AceView gene 5N792
        WormQTL gene WBGene00008218
        WormFlux gene WBGene00008218
        NDB locus_tag CELE_C50B6.2
        Panther gene CAEEL|WormBase=WBGene00008218|UniProtKB=O17687
          family PTHR15081
        NCBI gene 179810
        RefSeq protein NM_073897.8
        TREEFAM TREEFAM_ID TF317297
        TrEMBL UniProtAcc O17687
        UniProt_GCRP UniProtAcc O17687
    Species: Caenorhabditis elegans
    History: Version_change: 1 26 May 2004 16:54:48 WBPerson1971 Event: Imported: Initial conversion from CDS class of WS125
        2 31 May 2006 17:04:33 WBPerson2970 Name_change: CGC_name: nasp-2
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: nasp
    Allele (36)
    Strain: WBStrain00051233
    RNASeq_FPKM (74)
    GO_annotation: 00030380
      00030381
      00030382
      00030383
    Ortholog (34)
    Paralog: WBGene00007500 Caenorhabditis elegans From_analysis: Inparanoid_8
            Panther
            WormBase-Compara
    Structured_description: Automated_description: Predicted to enable histone binding activity. Predicted to be involved in CENP-A containing chromatin assembly and DNA replication-dependent chromatin assembly. Predicted to be located in nucleoplasm. Expressed in germ line. Human ortholog(s) of this gene implicated in ovarian cancer. Is an ortholog of human NASP (nuclear autoantigenic sperm protein). 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:2394 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:7644)
  Molecular_info: Corresponding_CDS: C50B6.2
    Corresponding_transcript: C50B6.2.1
    Other_sequence (12)
    Associated_feature: WBsf653301
      WBsf977328
      WBsf977329
      WBsf977330
      WBsf977331
      WBsf234789
      WBsf234790
  Experimental_info: RNAi_result: WBRNAi00007819 Inferred_automatically: RNAi_primary
      WBRNAi00012175 Inferred_automatically: RNAi_primary
      WBRNAi00077602 Inferred_automatically: RNAi_primary
      WBRNAi00030008 Inferred_automatically: RNAi_primary
      WBRNAi00042850 Inferred_automatically: RNAi_primary
    Expr_pattern: Chronogram411
      Expr4109
      Expr5542
      Expr1014574
      Expr1033570
      Expr1146829
      Expr2013894
      Expr2032134
    Drives_construct: WBCnstr00003950
      WBCnstr00033144
    Construct_product: WBCnstr00016401
      WBCnstr00033144
    Microarray_results (19)
    Expression_cluster (248)
    Interaction (316)
  Map_info: Map: V Position: 5.12268 Error: 0.002429
    Positive: Positive_clone: C50B6 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference: WBPaper00028554
    WBPaper00038491
    WBPaper00040521
    WBPaper00055090
    WBPaper00062002
  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