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WormBase Tree Display for Gene: WBGene00002050

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Name Class

WBGene00002050SMapS_parentSequenceCHROMOSOME_X
IdentityVersion1
NameCGC_nameifa-1Person_evidenceWBPerson105
WBPerson293
Sequence_nameF38B2.1
Molecular_nameF38B2.1a
F38B2.1a.1
CE31506
F38B2.1b
CE31507
F38B2.1c
CE05824
F38B2.1d
CE24961
F38B2.1e
CE53169
F38B2.1b.1
F38B2.1c.1
F38B2.1d.1
F38B2.1e.1
Other_nameCel IF A1Accession_evidenceEMBLX70834
CelIF a1
A1Paper_evidenceWBPaper00006137
CELE_F38B2.1Accession_evidenceNDBBX284606
Public_nameifa-1
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:26WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classifa
Allele (77)
StrainWBStrain00036052
RNASeq_FPKM (74)
GO_annotation (14)
Ortholog (65)
Paralog (12)
Structured_descriptionConcise_descriptionIFA-1 encodes an essential intermediate filament protein that is coexpressed with the essential IF protein IFB-1; IFA-1 is required for survival past the L1 larva stage, and a normal intestine; IFA-1 forms heteropolymeric intermediate filaments in vitro with an equimolar mixture of IFB-1; IFA-1 is predicted to function as a structural component of the cytoskeleton, and is required for larval development and normal intestinal morphology; ifa-1 is expressed in amphid sensory neurons, in tail neurons and other unidentified neurons, some pharyngeal muscles, the pharyngeal-intestinal valve, the vulva, and the rectum.Paper_evidenceWBPaper00001981
WBPaper00004761
WBPaper00006137
Curator_confirmedWBPerson1843
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to be a structural constituent of cytoskeleton. Predicted to be involved in cellular localization; heterochromatin formation; and nucleus organization. Located in intermediate filament. Expressed in several structures, including egg-laying apparatus; excretory cell; neurons; pharyngeal-intestinal valve; and pharynx. Human ortholog(s) of this gene implicated in partial lipodystrophy; primary autosomal recessive microcephaly; and progressive myoclonus epilepsy 9. Is an ortholog of human LMNB2 (lamin B2).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:0111450Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6638)
DOID:0070296Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6638)
DOID:0080299Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6638)
Molecular_infoCorresponding_CDSF38B2.1a
F38B2.1b
F38B2.1c
F38B2.1d
F38B2.1e
Corresponding_CDS_historyF38B2.1:wp83
Corresponding_transcriptF38B2.1a.1
F38B2.1b.1
F38B2.1c.1
F38B2.1d.1
F38B2.1e.1
Other_sequence (241)
Associated_feature (14)
Experimental_infoRNAi_result (48)
Expr_patternExpr1495
Expr2762
Expr1013956
Expr1031203
Expr1150559
Expr2012676
Expr2030912
Drives_constructWBCnstr00010937
WBCnstr00036494
Construct_productWBCnstr00010937
WBCnstr00036494
Microarray_results (39)
Expression_cluster (212)
InteractionWBInteraction000029165
WBInteraction000029769
WBInteraction000029777
WBInteraction000040908
WBInteraction000044847
WBInteraction000045233
WBInteraction000045534
WBInteraction000166840
WBInteraction000217940
WBInteraction000217941
WBInteraction000217942
WBInteraction000252137
WBInteraction000321662
WBInteraction000329052
WBInteraction000336891
WBInteraction000341912
WBInteraction000363732
WBInteraction000376785
WBInteraction000384172
WBInteraction000390888
WBInteraction000407470
WBInteraction000416207
WBInteraction000426075
WBInteraction000444153
WBInteraction000455290
WBInteraction000510188
WBInteraction000510814
WBInteraction000515079
WBInteraction000515109
WBInteraction000516758
WBInteraction000516791
WBInteraction000516962
WBInteraction000516982
WBInteraction000540542
WBInteraction000543134
WBInteraction000543675
WBInteraction000543931
WBInteraction000546171
WBInteraction000550721
WBInteraction000550734
WBInteraction000550801
WBInteraction000551452
WBInteraction000552794
WBInteraction000553874
WBInteraction000561736
WBInteraction000562238
WBInteraction000562357
WBInteraction000563381
WBInteraction000563386
WBInteraction000563387
WBInteraction000563388
WBInteraction000563389
WBInteraction000563390
WBInteraction000563391
WBInteraction000563392
WBInteraction000563393
WBInteraction000563394
WBInteraction000563395
WBInteraction000563955
WBInteraction000564582
WBInteraction000565342
WBInteraction000566231
WBInteraction000566510
WBInteraction000566777
WBInteraction000571715
WBInteraction000572520
WBInteraction000572758
WBInteraction000578781
WBInteraction000583012
WBInteraction000583741
WBInteraction000584100
WBInteraction000586592
Map_infoMapXPosition2.86537Error0.001386
PositivePositive_cloneF38B2Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4945
4421
4442
Pseudo_map_position
Reference (14)
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