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WormBase Tree Display for Gene: WBGene00018024

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Name Class

WBGene00018024SMapS_parentSequenceCHROMOSOME_X
IdentityVersion2
NameSequence_nameF35A5.1
Molecular_nameF35A5.1
F35A5.1.1
CE48053
Other_nameCELE_F35A5.1Accession_evidenceNDBBX284606
Public_nameF35A5.1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:59WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
207 Nov 2007 17:30:22WBPerson1849EventAcquires_mergeWBGene00019358
Acquires_mergeWBGene00019358
StatusLive
Gene_infoBiotypeSO:0001217
Allele (152)
StrainWBStrain00032549
RNASeq_FPKM (74)
GO_annotation00066799
00066800
00123289
00123290
Ortholog (24)
ParalogWBGene00015868Caenorhabditis elegansFrom_analysisTreeFam
Structured_descriptionConcise_descriptionThe F35A5.1 gene encodes a homolog of human FMR2, which when mutated leads to fragile site mental retardation, type 2 (OMIM:309548).Paper_evidenceWBPaper00004103
Curator_confirmedWBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to be a structural constituent of cytoskeleton. Predicted to be involved in intermediate filament bundle assembly. Predicted to be located in neurofilament. Human ortholog(s) of this gene implicated in several diseases, including Creutzfeldt-Jakob disease; autoimmune disease of the nervous system (multiple); and neuropathy (multiple). Is an ortholog of human NEFH (neurofilament heavy chain).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:8869Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7737)
DOID:2378Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7737)
DOID:7442Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7737)
DOID:2377Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7737)
DOID:1210Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7737)
DOID:0040089Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7737)
DOID:0110180Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7737)
DOID:11949Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7737)
DOID:332Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7737)
DOID:0060193Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7737)
Molecular_infoCorresponding_CDSF35A5.1
Corresponding_CDS_historyF35A5.1:wp184
F35A5.1:wp214
F35A5.1:wp234
Corresponding_transcriptF35A5.1.1
Other_sequence (29)
Associated_featureWBsf662623
WBsf662624
WBsf1022680
WBsf235529
Experimental_infoRNAi_resultWBRNAi00046264Inferred_automaticallyRNAi_primary
WBRNAi00049805Inferred_automaticallyRNAi_primary
WBRNAi00022586Inferred_automaticallyRNAi_primary
WBRNAi00016527Inferred_automaticallyRNAi_primary
WBRNAi00002126Inferred_automaticallyRNAi_primary
WBRNAi00014277Inferred_automaticallyRNAi_primary
WBRNAi00033913Inferred_automaticallyRNAi_primary
Expr_patternExpr1022847
Expr1037767
Expr1150154
Expr2003289
Expr2021502
Microarray_results (31)
Expression_cluster (175)
Interaction (29)
Map_infoPositivePositive_cloneF35A5Inferred_automaticallyFrom sequence, transcript, pseudogene data
Interpolated_map_positionX-9.35503
ReferenceWBPaper00038491
MethodGene