WormBase Tree Display for Gene: WBGene00008979

WBGene00008979 SMap: S_parent: Sequence: F20D1
  Identity: Version: 2
    Name: CGC_name: slc-25A18.1
      Sequence_name: F20D1.9
      Molecular_name: F20D1.9
        F20D1.9.1
        CE47961
      Other_name: CELE_F20D1.9 Accession_evidence: NDB BX284606
      Public_name: slc-25A18.1
    DB_info: Database (11)
    Species: Caenorhabditis elegans
    History: Version_change (2)
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: slc
    Allele: WBVar01499887
      WBVar01499519
      WBVar01499888
      WBVar01499710
      WBVar00085904
      WBVar00085905
      WBVar00319377
      WBVar01528218
      WBVar01528219
      WBVar01212097
      WBVar01528220
      WBVar01212098
      WBVar01212099
      WBVar01212100
      WBVar01212101
      WBVar01212102
      WBVar01212103
      WBVar01212104
      WBVar01212105
      WBVar01212106
      WBVar01212107
      WBVar01212108
      WBVar01212109
      WBVar01212110
      WBVar02146214
      WBVar01212111
      WBVar01212112
      WBVar01212113
      WBVar01212114
      WBVar00323086
      WBVar00321210
      WBVar00308554
      WBVar00313771
      WBVar00313772
      WBVar00525623
      WBVar01498960
      WBVar01500067
    RNASeq_FPKM (74)
    GO_annotation (11)
    Contained_in_operon: CEOPX132
    Ortholog (44)
    Paralog (35)
    Structured_description: Automated_description: Predicted to enable L-aspartate transmembrane transporter activity and L-glutamate transmembrane transporter activity. Predicted to be involved in L-glutamate transmembrane transport; aspartate transmembrane transport; and malate-aspartate shuttle. Predicted to be located in membrane. Human ortholog(s) of this gene implicated in developmental and epileptic encephalopathy 3. Is an ortholog of human SLC25A18 (solute carrier family 25 member 18) and SLC25A22 (solute carrier family 25 member 22). 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:0080440 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:19954)
  Molecular_info: Corresponding_CDS: F20D1.9
    Corresponding_CDS_history: F20D1.9:wp234
    Corresponding_transcript: F20D1.9.1
    Other_sequence (69)
    Associated_feature: WBsf1008064
      WBsf238279
  Experimental_info: RNAi_result: WBRNAi00013618 Inferred_automatically: RNAi_primary
      WBRNAi00076320 Inferred_automatically: RNAi_primary
      WBRNAi00094935 Inferred_automatically: RNAi_primary
      WBRNAi00045100 Inferred_automatically: RNAi_primary
      WBRNAi00023428 Inferred_automatically: RNAi_primary
      WBRNAi00117467 Inferred_automatically: RNAi_primary
      WBRNAi00024003 Inferred_automatically: RNAi_primary
      WBRNAi00023715 Inferred_automatically: RNAi_primary
      WBRNAi00031169 Inferred_automatically: RNAi_primary
      WBRNAi00023203 Inferred_automatically: RNAi_primary
    Expr_pattern: Chronogram1183
      Expr5804
      Expr14638
      Expr1026344
      Expr1033909
      Expr1149050
      Expr2002780
      Expr2020998
    Drives_construct: WBCnstr00004085
      WBCnstr00032549
      WBCnstr00041189
    Construct_product: WBCnstr00032549
      WBCnstr00041189
    Microarray_results (18)
    Expression_cluster (131)
    Interaction (51)
  Map_info: Map: X Position: 21.7444
    Positive: Positive_clone: F20D1 Inferred_automatically: From sequence, transcript, pseudogene data
    Pseudo_map_position
  Reference: WBPaper00038491
    WBPaper00055090
    WBPaper00059575
    WBPaper00061547
  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