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WormBase Tree Display for Gene: WBGene00001400

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Name Class

WBGene00001400SMapS_parentSequenceF56E3
IdentityVersion1
NameCGC_namefax-1Person_evidenceWBPerson691
Sequence_nameF56E3.4
Molecular_nameF56E3.4a
F56E3.4a.1
CE28464
F56E3.4b
CE04670
F56E3.4b.1
Other_namenhr-29
CELE_F56E3.4Accession_evidenceNDBBX284606
Public_namefax-1
DB_infoDatabaseAceViewgeneXD816
WormQTLgeneWBGene00001400
WormFluxgeneWBGene00001400
NDBlocus_tagCELE_F56E3.4
PanthergeneCAEEL|WormBase=WBGene00001400|UniProtKB=G5EDJ0
familyPTHR24083
NCBIgene180609
RefSeqproteinNM_001277024.2
NM_076146.4
SwissProtUniProtAccG5EDJ0
UniProt_GCRPUniProtAccG5EDJ0
OMIMgene604485
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:24WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classfax
AlleleWBVar00146315Inferred_automaticallyFrom strain object: NG2267
WBVar00275427
WBVar01813985
WBVar02026892
WBVar02044474
WBVar00076967
WBVar01132112
WBVar01132113
WBVar01468213
WBVar01132114
WBVar01132115
WBVar01132116
WBVar01132117
WBVar01132118
WBVar00254938
WBVar01132119
WBVar01132120
WBVar01132121
WBVar01132122
WBVar01132123
WBVar01132124
WBVar01132125
WBVar01132126
WBVar01132127
WBVar01132128
WBVar01132129
WBVar01132130
WBVar01491138
WBVar01132131
WBVar01132132
WBVar01132133
WBVar01132134
WBVar01132135
WBVar01132136
WBVar01132137
WBVar01132138
WBVar01132139
WBVar00498501
WBVar00498502
WBVar00498503
WBVar00498504
WBVar00498505
WBVar00498506
WBVar00498507
WBVar00498508
WBVar00498509
WBVar00498510
WBVar00498511
WBVar00498512
WBVar00498513
WBVar00091908
WBVar00498514
WBVar00498515
WBVar01499636
WBVar00146327
WBVar01822426
WBVar01822427
Legacy_information[Wightman B] Mutations cause a weak kinker phenotype and defects in axon guidance of HSNL, AVKR, PVQL axons.
[Wightman B] encoded by F56E3.4 nuclear hormone receptor, mutants are Unc, egg-laying constitutive, and have defects in axon pathfinding in the ventral nerve cord.
StrainWBStrain00027632
WBStrain00001394
WBStrain00027630
WBStrain00028736
WBStrain00028744
WBStrain00031525
RNASeq_FPKM (74)
GO_annotation (33)
Ortholog (34)
Paralog (43)
Structured_descriptionConcise_descriptionfax-1 encodes a conserved nuclear receptor that contains two C4-type zinc fingers and is orthologous to the vertebrate photoreceptor-specific nuclear receptor PNR (OMIM:604485, mutated in enhanced S-cone syndrome and retinitis pigmentosa); fax-1 is required for normal locomotion and neuron fate specification, including specification of the AVA, AVE, and AVK interneurons and proper axon pathfinding of the AVK, HSNL, and PVQL axons; expression of reporter gene fusions in fax-1 mutants suggests that fax-1 functions by regulating expression of a number of downstream targets, including nmr-1 and nmr-2, opt-3, flp-1, and ncs-1; in some neurons, fax-1 regulates expression combinatorially with unc-42, which encodes a paired-like homeodomain protein that additionally, regulates fax-1 expression in AVK neurons; FAX-1 exhibits sequence-specific DNA binding in vitro and the FAX-1 DNA binding domain, when fused to the GAL4 transcriptional activator, can positively regulate transcription in yeast one-hybrid assays; FAX-1 is expressed in the nuclei of 18 neurons, including the AVK, AVA, AVB, and AVE interneurons, beginning at mid-embryogenesis and continuing through larval and adult stages; FAX-1 is also seen in two non-neuronal cell types: the distal tip cells (DTCs), from L2 to L4 larval stages, and two pairs of vulval cells in L4 animals.Paper_evidenceWBPaper00003941
WBPaper00026828
WBPaper00031380
Curator_confirmedWBPerson1843
WBPerson1823
WBPerson567
Date_last_updated09 Oct 2008 00:00:00
Automated_descriptionEnables DNA-binding transcription factor activity, RNA polymerase II-specific and sequence-specific DNA binding activity. Involved in several processes, including neuron differentiation; positive regulation of transcription by RNA polymerase II; and regulation of locomotion. Located in nucleus. Expressed in several structures, including CEP; hermaphrodite distal tip cell; interneuron; pharyngeal motor neurons; and rect_D. Human ortholog(s) of this gene implicated in enhanced S-cone syndrome and retinitis pigmentosa 37. Is an ortholog of human NR2E3 (nuclear receptor subfamily 2 group E member 3).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_infoPotential_modelDOID:0090059Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7974)
DOID:0110399Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7974)
Molecular_infoCorresponding_CDSF56E3.4a
F56E3.4b
Corresponding_transcriptF56E3.4a.1
F56E3.4b.1
Other_sequenceSRC02099_1
Acan_isotig10071
EY464040.1
SR01788
FC815338.1
JI475021.1
CRC12381_1
JI170219.1
Associated_feature (11)
Transcription_factorWBTranscriptionFactor000521
Experimental_infoRNAi_resultWBRNAi00027911Inferred_automaticallyRNAi_primary
WBRNAi00048731Inferred_automaticallyRNAi_primary
WBRNAi00115862Inferred_automaticallyRNAi_primary
WBRNAi00015835Inferred_automaticallyRNAi_primary
WBRNAi00048732Inferred_automaticallyRNAi_primary
WBRNAi00015837Inferred_automaticallyRNAi_primary
Expr_pattern (12)
Drives_constructWBCnstr00002284
WBCnstr00004291
WBCnstr00012731
WBCnstr00013827
WBCnstr00036970
Construct_productWBCnstr00013827
WBCnstr00021906
WBCnstr00036970
AntibodyWBAntibody00000945
WBAntibody00002352
Microarray_results (22)
Expression_cluster (108)
Interaction (20)
Map_infoMapXPosition-10.7537Error0.119879
Well_ordered
PositiveInside_rearrsyDf1
yDp14
Positive_cloneC02A6Author_evidenceWightman BC
C38F12Author_evidenceWightman BC
F56E3Author_evidenceWightman BC
Inferred_automaticallyFrom sequence, transcript, pseudogene data
W05A4Author_evidenceWightman BC
NegativeNegative_cloneC15C7Author_evidenceWightman BC
F28B4Author_evidenceWightman BC
F40F4Author_evidenceWightman BC
Mapping_dataMulti_point3537
3538
3539
3696
5603
Pos_neg_data9117
9118
Reference (56)
MethodGene