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WormBase Tree Display for Gene: WBGene00001432

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Name Class

WBGene00001432SMapS_parentSequenceCHROMOSOME_I
IdentityVersion1
NameCGC_namefkb-7Person_evidenceWBPerson466
Sequence_nameB0511.1
Molecular_nameB0511.1
B0511.1.1
CE26851
Other_nameCELE_B0511.1Accession_evidenceNDBBX284601
Public_namefkb-7
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:24WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classfkb
Allele (38)
Legacy_information[Page AP] B0511.1 No mutants known.
RNASeq_FPKM (74)
GO_annotation00036419
00036420
00036421
00036422
00036423
00036424
00108698
Ortholog (43)
ParalogWBGene00001426Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001427Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001428Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001429Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001430Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001431Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001433Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionfkb-7 encodes a peptidylprolyl cis/trans isomerase homologous to mammalian FK506-binding proteins; by homology, FKB-7 could function in a number of different processes including protein folding, signal transduction, and regulation of muscle contraction; however, as loss of fkb-7 function via RNA-mediated interference (RNAi) does not result in any obvious abnormalities, the precise role of FKB-7 in C. elegans development and/or behavior is not yet known.Paper_evidenceWBPaper00004285
WBPaper00004402
Curator_confirmedWBPerson1843
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable peptidyl-prolyl cis-trans isomerase activity. Human ortholog(s) of this gene implicated in Ehlers-Danlos syndrome kyphoscoliotic type 2. Is an ortholog of human FKBP14 (FKBP prolyl isomerase 14) and FKBP7 (FKBP prolyl isomerase 7).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:0080735Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18625)
Molecular_infoCorresponding_CDSB0511.1
Corresponding_transcriptB0511.1.1
Other_sequence (27)
Associated_featureWBsf643705
WBsf656893
WBsf985054
WBsf218472
Experimental_infoRNAi_resultWBRNAi00003073Inferred_automaticallyRNAi_primary
WBRNAi00116495Inferred_automaticallyRNAi_primary
WBRNAi00115760Inferred_automaticallyRNAi_primary
WBRNAi00002859Inferred_automaticallyRNAi_primary
WBRNAi00076058Inferred_automaticallyRNAi_primary
WBRNAi00039137Inferred_automaticallyRNAi_primary
WBRNAi00115895Inferred_automaticallyRNAi_primary
Expr_patternExpr16139
Expr1022076
Expr1030857
Expr1143294
Expr2011801
Expr2030039
Drives_constructWBCnstr00036953
Construct_productWBCnstr00036953
Microarray_results (20)
Expression_cluster (248)
Interaction (36)
Map_infoMapIPosition5.06033Error0.000114
PositivePositive_cloneB0511Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00004285
WBPaper00026884
WBPaper00038491
WBPaper00055090
WBPaper00062388
WBPaper00064339
RemarkACeDB prediction of first exon is incorrect -- see intronerator entry g-I-1963
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