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WormBase Tree Display for Gene: WBGene00017973

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Name Class

WBGene00017973SMapS_parentSequenceF32A6
IdentityVersion2
NameCGC_nameift-81Person_evidenceWBPerson426
Sequence_nameF32A6.2
Molecular_nameF32A6.2
F32A6.2.1
CE41565
Other_nameCELE_F32A6.2Accession_evidenceNDBBX284606
Public_nameift-81
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:59WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
219 Sep 2007 10:26:44WBPerson1849EventAcquires_mergeWBGene00017972
Name_changeCGC_nameift-81
Acquires_mergeWBGene00017972
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classift
Allele (143)
StrainWBStrain00002530
WBStrain00036344
WBStrain00036504
WBStrain00007576
WBStrain00051699
RNASeq_FPKM (74)
GO_annotation (16)
Ortholog (32)
Structured_descriptionConcise_descriptionift-81 encodes an ortholog of the intraflagellar transport component IFT-81 in Chlamydomonas; ift-81 along with ift-74 is involved in growth, chemotaxis, intraflagellar transport and the morphogenesis of cilia; ift-81 binds ift-74 in protein binding assays and co-localizes with ift-74 to the transition zone of cilia in neurons, indicating that ift-81 may form a complex with ift-74.Paper_evidenceWBPaper00030726
Curator_confirmedWBPerson324
Date_last_updated27 Oct 2008 00:00:00
Automated_descriptionEnables microtubule binding activity. Involved in chemotaxis; detection of stimulus involved in sensory perception; and intraciliary transport. Located in non-motile cilium. Expressed in amphid neurons; chemosensory neurons; and phasmid neurons. Human ortholog(s) of this gene implicated in short-rib thoracic dysplasia 19 with or without polydactyly. Is an ortholog of human IFT81 (intraflagellar transport 81).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:0080295Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:14313)
Molecular_infoCorresponding_CDSF32A6.2
Corresponding_CDS_historyF32A6.2:wp99
F32A6.2:wp182
F32A6.2:wp191
F32A6.2:wp196
F32A6.2:wp213
Corresponding_transcriptF32A6.2.1
Other_sequenceEL890803.1
BM01040
Associated_feature (5)
Experimental_infoRNAi_resultWBRNAi00031647Inferred_automaticallyRNAi_primary
WBRNAi00046081Inferred_automaticallyRNAi_primary
WBRNAi00046082Inferred_automaticallyRNAi_primary
WBRNAi00014197Inferred_automaticallyRNAi_primary
Expr_patternExpr4638
Expr5927
Expr8322
Expr1026677
Expr1037733
Expr1149971
Expr2012699
Expr2030935
Drives_constructWBCnstr00003106
WBCnstr00012142
WBCnstr00013259
Construct_productWBCnstr00013259
Microarray_results (37)
Expression_cluster (195)
Interaction (17)
Map_infoMapXPosition-5.72774Error0.007898
PositivePositive_cloneF32A6Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00026601
WBPaper00028949
WBPaper00029016
WBPaper00030726
WBPaper00031170
WBPaper00037724
WBPaper00038491
WBPaper00051562
WBPaper00055090
WBPaper00056552
WBPaper00063946
WBPaper00064360
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