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WormBase Tree Display for Gene: WBGene00006775

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Name Class

WBGene00006775SMapS_parentSequenceF56A12
IdentityVersion2
NameCGC_nameunc-39Person_evidenceWBPerson261
Sequence_nameF56A12.1
Molecular_nameF56A12.1
F56A12.1.1
CE37921
Other_namemig-3
ceh-35Paper_evidenceWBPaper00024327
CELE_F56A12.1Accession_evidenceNDBBX284605
Public_nameunc-39
DB_infoDatabaseAceViewgene5O855
WormQTLgeneWBGene00006775
WormFluxgeneWBGene00006775
OMIMdisease610896
160900
gene600963
NDBlocus_tagCELE_F56A12.1
PanthergeneCAEEL|WormBase=WBGene00006775|UniProtKB=O17894
familyPTHR10390
NCBIgene191623
RefSeqproteinNM_074162.3
SwissProtUniProtAccO17894
UniProt_GCRPUniProtAccO17894
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:42WBPerson1971EventImportedInitial conversion from geneace
209 Nov 2004 14:53:34WBPerson2970EventAcquires_mergeWBGene00000456
Acquires_mergeWBGene00000456
StatusLive
Gene_info (11)
Disease_infoExperimental_modelDOID:11722Homo sapiensPaper_evidenceWBPaper00024327
Accession_evidenceOMIM160900
Curator_confirmedWBPerson324
Date_last_updated24 Oct 2013 00:00:00
DOID:14702Homo sapiensPaper_evidenceWBPaper00024327
Accession_evidenceOMIM610896
Curator_confirmedWBPerson324
Date_last_updated24 Oct 2013 00:00:00
Potential_modelDOID:0111424Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10891)
Disease_relevanceMutations in the human Six5 protein have been implicated in Myotonic dystrophy 1 (DM1), a highly variable disease characterized by progressive muscle wasting, eye cataracts, cardiac abnormalities, and insulin resistance; in C. elegans, mutants in unc-29 (e257), orthologous to human Six5, show uncoordinated movement, mesodermal defects, and neuronal developmental and pathfinding defects; these studies indicate that unc-29/Six5 may be involved in development of mesoderm and differentiation and migration of neurons; the variable expressivity and penetrance of unc-39 defects are reminiscent of the pleiotropy seen in DM1 patients; some of the unc-29 mutant defects (coelomocyte specification) could be rescued by a transgene containing Six domain and homeodomain coding region from human Six5, showing a functional conservation between unc-29 and Six5; these studies indicate that unc-29 serves as a model to study how Six5 plays a role in conditions leading to myotonic dystrophy.Homo sapiensPaper_evidenceWBPaper00024327
Accession_evidenceOMIM600963
160900
610896
Curator_confirmedWBPerson324
Date_last_updated01 May 2014 00:00:00
Models_disease_assertedWBDOannot00000238
WBDOannot00000299
Molecular_infoCorresponding_CDSF56A12.1
Corresponding_CDS_historyF56A12.1:wp137
Corresponding_transcriptF56A12.1.1
Other_sequenceAcan_isotig06578
Dviv_isotig15575
Dviv_isotig15576
Acan_isotig06577
Oden_isotig18067
Tcir_isotig25512
Oden_isotig25907
JI463737.1
Oden_isotig18066
JI211494.1
Associated_featureWBsf647528
WBsf662081
WBsf662082
WBsf662083
WBsf978863
WBsf1001995
WBsf1020832
WBsf232919
WBsf232920
Gene_product_binds (218)
Transcription_factorWBTranscriptionFactor000219
Experimental_infoRNAi_resultWBRNAi00101784Inferred_automaticallyRNAi_primary
WBRNAi00032912Inferred_automaticallyRNAi_primary
WBRNAi00089718Inferred_automaticallyRNAi_primary
WBRNAi00090158Inferred_automaticallyRNAi_primary
WBRNAi00090317Inferred_automaticallyRNAi_primary
WBRNAi00061182Inferred_automaticallyRNAi_primary
WBRNAi00015762Inferred_automaticallyRNAi_primary
WBRNAi00048581Inferred_automaticallyRNAi_primary
WBRNAi00114716Inferred_automaticallyRNAi_primary
WBRNAi00089999Inferred_automaticallyRNAi_primary
Expr_pattern (12)
Drives_constructWBCnstr00004349
WBCnstr00011130
WBCnstr00012730
WBCnstr00015880
WBCnstr00016522
WBCnstr00034159
Construct_productWBCnstr00011130
WBCnstr00015880
WBCnstr00016701
WBCnstr00034159
Regulate_expr_clusterWBPaper00050496:unc-39(hp701)_regulated
Microarray_results (20)
Expression_cluster (153)
Interaction (134)
Map_infoMapVPosition6.28117Error0.001023
PositivePositive_cloneF56A12Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_data2_point132
839
1725
Multi_point (14)
Pos_neg_data297
2131
3132
4308
ReferenceWBPaper00000031
WBPaper00000608
WBPaper00000978
WBPaper00001304
WBPaper00001411
WBPaper00001461
WBPaper00001508
WBPaper00004825
WBPaper00004883
WBPaper00015049
WBPaper00015440
WBPaper00015723
WBPaper00016590
WBPaper00017575
WBPaper00018929
WBPaper00018930
WBPaper00023095
WBPaper00024327
WBPaper00027262
WBPaper00027309
WBPaper00029033
WBPaper00029053
WBPaper00029055
WBPaper00032446
WBPaper00033137
WBPaper00039624
WBPaper00047468
WBPaper00050496
WBPaper00056066
WBPaper00057619
WBPaper00058964
WBPaper00060123
WBPaper00061738
WBPaper00064421
WBPaper00064694
MethodGene