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WormBase Tree Display for Gene: WBGene00016173

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Name Class

WBGene00016173SMapS_parentSequenceC27H5
IdentityVersion2
NameCGC_namefust-1Person_evidenceWBPerson1352
Sequence_nameC27H5.3
Molecular_nameC27H5.3a
C27H5.3a.1
CE27099
C27H5.3b
CE51847
C27H5.3b.1
C27H5.3b.2
Other_nameCELE_C27H5.3Accession_evidenceNDBBX284602
Public_namefust-1
DB_infoDatabaseAceViewgene2H445
WormQTLgeneWBGene00016173
WormFluxgeneWBGene00016173
NDBlocus_tagCELE_C27H5.3
PanthergeneCAEEL|WormBase=WBGene00016173|UniProtKB=Q18265
familyPTHR23238
NCBIgene174175
RefSeqproteinNM_063082.7
NM_001381492.1
TrEMBLUniProtAccQ18265
A0A1N7SYQ6
UniProt_GCRPUniProtAccQ18265
OMIMgene133450
137070
601574
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:57WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
203 Aug 2010 10:05:58WBPerson2970Name_changeCGC_namefust-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classfust
Allele (42)
StrainWBStrain00001567
WBStrain00047288
WBStrain00047287
WBStrain00047289
WBStrain00050865
RNASeq_FPKM (74)
GO_annotation (11)
Ortholog (47)
Structured_descriptionAutomated_descriptionPredicted to enable RNA binding activity and transcription coregulator activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. Expressed in gonad; head; intestinal cell; neurons; and tail. Human ortholog(s) of this gene implicated in amyotrophic lateral sclerosis type 6; connective tissue cancer (multiple); and essential tremor 4. Is an ortholog of human FUS (FUS RNA binding protein).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:1289Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4010)
DOID:0111431Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4010)
DOID:0060198Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4010)
DOID:4549Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11547)
DOID:1115Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4010)
DOID:332Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4010)
DOID:3382Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4010)
DOID:3371Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11547)
DOID:3369Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3508)
Molecular_infoCorresponding_CDSC27H5.3a
C27H5.3b
Corresponding_transcriptC27H5.3a.1
C27H5.3b.1
C27H5.3b.2
Other_sequence (37)
Associated_featureWBsf644354
WBsf988367
WBsf221563
Experimental_infoRNAi_resultWBRNAi00090580Inferred_automaticallyRNAi_primary
WBRNAi00011275Inferred_automaticallyRNAi_primary
WBRNAi00083277Inferred_automaticallyRNAi_primary
WBRNAi00076171Inferred_automaticallyRNAi_primary
WBRNAi00041374Inferred_automaticallyRNAi_primary
Expr_pattern (11)
Drives_constructWBCnstr00002407
WBCnstr00028273
WBCnstr00042661
WBCnstr00042662
WBCnstr00042663
Construct_productWBCnstr00028273
WBCnstr00042661
WBCnstr00042662
WBCnstr00042663
Regulate_expr_clusterWBPaper00066004:fust-1(csb21)_downregulated
WBPaper00066004:fust-1(csb21)_upregulated
Microarray_results (19)
Expression_cluster (109)
Interaction (197)
Map_infoMapIIPosition0.496031Error0.000218
PositivePositive_cloneC27H5Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00039140
WBPaper00043234
WBPaper00046432
WBPaper00052702
WBPaper00053121
WBPaper00053757
WBPaper00055090
WBPaper00058116
WBPaper00062110
WBPaper00063415
WBPaper00063450
WBPaper00064663
WBPaper00066004
WBPaper00066342
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