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WormBase Tree Display for Gene: WBGene00003623

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Name Class

WBGene00003623EvidencePaper_evidenceWBPaper00003416
WBPaper00004124
WBPaper00004329
SMapS_parentSequenceF11C1
IdentityVersion1
NameCGC_namenhr-25Person_evidenceWBPerson600
Sequence_nameF11C1.6
Molecular_nameF11C1.6a
F11C1.6a.1
CE03191
F11C1.6b
CE35856
F11C1.6a.2
F11C1.6b.1
Other_nameCELE_F11C1.6Accession_evidenceNDBBX284606
Public_namenhr-25
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:32WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classnhr
Allele (94)
Legacy_information[M Asahina] jm2389 is mutagenized using TMP/UV and detected a deletion by PCR. This removes the coding region from Gly40 in the P-box of the first zinc finger motif to Ser377 in the middle of the conserved region II within the LBD (ref. Asahina M et al. 2000 The conserved nuclear receptor Ftz-F1 is required for embryogenesis, moulting and reproduction in Caenorhabditis elegans. Genes to Cells 5: 711). Phenotype is homozygous embryonic lethal at 1.5-fold to 2-fold stage. Balanced with +/szT1[lon-2(e678)] I; nDf19/szT1 X (strain MT1401)
Strain (13)
RNASeq_FPKM (74)
GO_annotation (26)
Ortholog (52)
Paralog (17)
Structured_description (2)
Disease_infoPotential_modelDOID:0111764Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7983)
DOID:905Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7983)
DOID:0070169Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7983)
DOID:0111772Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7983)
DOID:0080864Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7983)
DOID:219Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7984)
Molecular_infoCorresponding_CDSF11C1.6a
F11C1.6b
Corresponding_transcriptF11C1.6a.1
F11C1.6a.2
F11C1.6b.1
Other_sequence (13)
Associated_feature (24)
Gene_product_binds (378)
Transcription_factorWBTranscriptionFactor000597
Experimental_infoRNAi_result (143)
Expr_pattern (27)
Drives_construct (13)
Construct_product (13)
Regulate_expr_clusterWBPaper00045015:nhr-25(RNAi)_downregulated
WBPaper00045015:nhr-25(RNAi)_upregulated
AntibodyWBAntibody00000832
WBAntibody00002489
Microarray_results (31)
Expression_cluster (213)
Interaction (111)
Product_binds_matrixWBPmat00005568
WBPmat00005572
Map_infoMapXPosition9.49412Error0.083721
PositivePositive_cloneF11C1Person_evidenceWBPerson29
Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4522
4883
5332
Pseudo_map_position
Reference (96)
RemarkMap 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