WormBase Tree Display for Gene: WBGene00002050

WBGene00002050 SMap: S_parent: Sequence: CHROMOSOME_X
  Identity: Version: 1
    Name: CGC_name: ifa-1 Person_evidence: WBPerson105
            WBPerson293
      Sequence_name: F38B2.1
      Molecular_name (15)
      Other_name: Cel IF A1 Accession_evidence: EMBL X70834
        CelIF a1
        A1 Paper_evidence: WBPaper00006137
        CELE_F38B2.1 Accession_evidence: NDB BX284606
      Public_name: ifa-1
    DB_info: Database (12)
    Species: Caenorhabditis elegans
    History: Version_change: 1 07 Apr 2004 11:29:26 WBPerson1971 Event: Imported: Initial conversion from geneace
    Status: Live
  Gene_info: Biotype: SO:0001217
    Gene_class: ifa
    Allele: WBVar01186777
      WBVar01186778
      WBVar01186779
      WBVar01499887
      WBVar01186780
      WBVar01690402
      WBVar01186781
      WBVar01499888
      WBVar01186782
      WBVar01186783
      WBVar01186784
      WBVar01186785
      WBVar01186786
      WBVar00092503
      WBVar01186787
      WBVar01499710
      WBVar01186788
      WBVar01186789
      WBVar01186790
      WBVar01186791
      WBVar01186792
      WBVar01186793
      WBVar01186794
      WBVar00083093
      WBVar02009110
      WBVar02009111
      WBVar02083479
      WBVar01496635
      WBVar01620543
      WBVar00067850
      WBVar01620544
      WBVar01620545
      WBVar01620546
      WBVar00067855
      WBVar00067860
      WBVar00517064
      WBVar00517065
      WBVar00517066
      WBVar00517067
      WBVar00517068
      WBVar00517069
      WBVar00517070
      WBVar00517071
      WBVar00517072
      WBVar01759446
      WBVar00275701
      WBVar02152302
      WBVar00257410
      WBVar01782572
      WBVar01186751
      WBVar01186752
      WBVar01186753
      WBVar01186754
      WBVar01186755
      WBVar01186756
      WBVar01186757
      WBVar01186758
      WBVar01186759
      WBVar01186760
      WBVar01186761
      WBVar01186762
      WBVar01186763
      WBVar01186764
      WBVar01186765
      WBVar01186766
      WBVar01186767
      WBVar01186768
      WBVar01186769
      WBVar01186770
      WBVar01186771
      WBVar01186772
      WBVar01186773
      WBVar01498960
      WBVar01186774
      WBVar01186775
      WBVar01500067
      WBVar01186776
    Strain: WBStrain00036052
    RNASeq_FPKM (74)
    GO_annotation (14)
    Ortholog (65)
    Paralog (12)
    Structured_description (2)
  Disease_info: Potential_model: DOID:0111450 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:6638)
      DOID:0070296 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:6638)
      DOID:0080299 Homo sapiens Inferred_automatically: Inferred by orthology to human genes with DO annotation (HGNC:6638)
  Molecular_info: Corresponding_CDS: F38B2.1a
      F38B2.1b
      F38B2.1c
      F38B2.1d
      F38B2.1e
    Corresponding_CDS_history: F38B2.1:wp83
    Corresponding_transcript: F38B2.1a.1
      F38B2.1b.1
      F38B2.1c.1
      F38B2.1d.1
      F38B2.1e.1
    Other_sequence (241)
    Associated_feature (14)
  Experimental_info: RNAi_result (48)
    Expr_pattern: Expr1495
      Expr2762
      Expr1013956
      Expr1031203
      Expr1150559
      Expr2012676
      Expr2030912
    Drives_construct: WBCnstr00010937
      WBCnstr00036494
    Construct_product: WBCnstr00010937
      WBCnstr00036494
    Microarray_results (39)
    Expression_cluster (212)
    Interaction (72)
  Map_info: Map: X Position: 2.86537 Error: 0.001386
    Positive: Positive_clone: F38B2 Inferred_automatically: From sequence, transcript, pseudogene data
    Mapping_data: Multi_point: 4945
        4421
        4442
    Pseudo_map_position
  Reference (14)
  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