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WormBase Tree Display for Gene: WBGene00001049

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Name Class

WBGene00001049SMapS_parentSequenceF33H2
IdentityVersion1
NameCGC_namedog-1Person_evidenceWBPerson533
Sequence_nameF33H2.1
Molecular_nameF33H2.1
F33H2.1.1
CE17764
Other_nameCELE_F33H2.1Accession_evidenceNDBBX284601
Public_namedog-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:22WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classdog
Allele (117)
StrainWBStrain00001778
WBStrain00003477
WBStrain00035483
RNASeq_FPKM (74)
GO_annotation (25)
Contained_in_operonCEOP1772
Ortholog (43)
Paralog (4)
Structured_descriptionConcise_descriptiondog-1 encodes a helicase homologous to the human FANCJ/BRIP1/BACH1 helicase; DOG-1 is required for interstrand cross-link (ICL) repair and for maintenance of polyguanine tracts of germline and somatic DNA by resolving the secondary structure that can occur in guanine-rich DNA during lagging-strand DNA synthesis; genetic analysis suggests that dog-1 functions downstream of fcd-2 and rad-51 in mediating ICL and that fcd-2 activity is required for G/C tract maintenance in the absence of dog-1.Paper_evidenceWBPaper00005308
WBPaper00031336
Curator_confirmedWBPerson48
WBPerson1843
WBPerson1823
WBPerson567
Date_last_updated25 May 2011 00:00:00
Automated_descriptionPredicted to enable DNA helicase activity. Involved in DNA metabolic process; regulation of DNA-templated DNA replication; and reproduction. Predicted to be located in nucleus. Expressed in head and tail. Used to study Fanconi anemia. Human ortholog(s) of this gene implicated in several diseases, including Alzheimer's disease; Down syndrome; Fanconi anemia complementation group J; and cervical squamous cell carcinoma. Is an ortholog of human BRIP1 (BRCA1 interacting helicase 1).Paper_evidenceWBPaper00065943
Curator_confirmedWBPerson324
WBPerson37462
Inferred_automaticallyThis description was generated automatically by a script based on data from the WS291 version of WormBase
Date_last_updated29 Nov 2023 00:00:00
Disease_infoExperimental_modelDOID:13636Homo sapiensPaper_evidenceWBPaper00031336
Accession_evidenceOMIM227650
Curator_confirmedWBPerson324
Date_last_updated05 Mar 2018 00:00:00
Potential_modelDOID:10652Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:20473)
DOID:9256Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:20473)
DOID:14250Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:20473)
DOID:3459Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:20473)
DOID:3744Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:20473)
DOID:1588Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:20473)
DOID:1612Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:20473)
DOID:0111097Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:20473)
Disease_relevanceHuman FANCJ/BRIP1/BACH1 encodes a dead-box helicase and BRCA1-binding protein mutated in Fanconi anemia (FA) and early-onset breast cancer; Fanconi anemia is a disorder characterized by genomic instability and cellular hypersensitivity to chemicals that generate DNA interstrand cross-links (ICLs); studies in C.elegans indicate that dog-1, the C. elegans functional orthlog of FANCJ, functions to maintain G-rich DNA and reduce ICL-induced damage, together with other FA pathway components.Homo sapiensPaper_evidenceWBPaper00041180
Curator_confirmedWBPerson324
Models_disease_assertedWBDOannot00000099
WBDOannot00000493
WBDOannot00000494
Molecular_infoCorresponding_CDSF33H2.1
Corresponding_transcriptF33H2.1.1
Other_sequenceOVC00605_1
Tcol_isotig13707
Oden_isotig24726
Oden_isotig26284
JI471429.1
Dviv_isotig24643
FC553114.1
Oden_isotig20671
JI165262.1
FC555167.1
PPC02977_1
AI046018.1
Oden_isotig22682
EX559653.1
Acan_isotig08813
CR10734
FC551269.1
FC550226.1
FC550475.1
ACC06976_1
Oden_isotig29291
ACC07922_1
CRC04921_1
Associated_featureWBsf649787
WBsf665194
WBsf220678
Experimental_infoRNAi_result (11)
Expr_patternChronogram442
Chronogram788
Expr5942
Expr5943
Expr1021031
Expr1030661
Expr1150126
Expr2011023
Expr2029260
Drives_constructWBCnstr00002591
WBCnstr00004379
WBCnstr00037121
Construct_productWBCnstr00037121
Microarray_results (19)
Expression_cluster (140)
InteractionWBInteraction000052805
WBInteraction000052900
WBInteraction000161806
WBInteraction000161819
WBInteraction000163067
WBInteraction000351166
WBInteraction000372486
WBInteraction000441914
WBInteraction000500003
WBInteraction000500004
Map_infoMapIPosition29.4332Error0.084094
PositivePositive_cloneF33H2Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4499
Pseudo_map_position
ReferenceWBPaper00005308
WBPaper00018773
WBPaper00019722
WBPaper00023755
WBPaper00024047
WBPaper00024048
WBPaper00024843
WBPaper00025829
WBPaper00026015
WBPaper00026040
WBPaper00026428
WBPaper00027172
WBPaper00027223
WBPaper00027589
WBPaper00027594
WBPaper00028397
WBPaper00028462
WBPaper00030458
WBPaper00030688
WBPaper00030838
WBPaper00031177
WBPaper00031336
WBPaper00031806
WBPaper00031945
WBPaper00032105
WBPaper00032410
WBPaper00034590
WBPaper00034815
WBPaper00035885
WBPaper00036433
WBPaper00038491
WBPaper00038681
WBPaper00038692
WBPaper00039653
WBPaper00040261
WBPaper00041180
WBPaper00041255
WBPaper00042654
WBPaper00044797
WBPaper00045722
WBPaper00046100
WBPaper00046668
WBPaper00049914
WBPaper00052040
WBPaper00053104
WBPaper00055090
WBPaper00057518
WBPaper00061557
WBPaper00062246
WBPaper00066019
RemarkSequence connection from [Cheung I, Schertzer M, Rose A, Lansdorp RM], [020809 krb]
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
MethodGene