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WormBase Tree Display for Gene: WBGene00003064

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Name Class

WBGene00003064EvidencePaper_evidenceWBPaper00005707
SMapS_parentSequenceR10H10
IdentityVersion2
NameCGC_namenfu-1Person_evidenceWBPerson205
Author_evidenceP. Kropp
Sequence_nameR10H10.1
Molecular_nameR10H10.1
R10H10.1.1
CE53043
Other_nameldp-8
CELE_R10H10.1Accession_evidenceNDBBX284604
Public_namenfu-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:30WBPerson1971EventImportedInitial conversion from geneace
219 Apr 2021 01:27:01WBPerson1983Name_changeCGC_namenfu-1
Other_nameldp-8
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classnfu
Allele (21)
Possibly_affected_byWBVar02157210
WBVar02157211
WBVar02157212
WBVar02157213
WBVar02157214
WBVar02157215
WBVar02158607
StrainWBStrain00049819
RNASeq_FPKM (74)
GO_annotation00073274
00073275
00073276
00073277
00073278
00073279
00073280
00110539
00110540
00110541
Contained_in_operonCEOP4376
Ortholog (40)
Structured_descriptionConcise_descriptionlpd-8 encodes a homolog of human and mouse HIRA-interacting protein-5; LPD-8 has C-terminal similarity to a domain of NifU observed in thioredoxin-like proteins and domains (COG0694), and is predicted to be mitochondrial on phylogenetic grounds.Paper_evidenceWBPaper00004133
WBPaper00004424
WBPaper00012874
Curator_confirmedWBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable 4 iron, 4 sulfur cluster binding activity and iron ion binding activity. Involved in lipid storage. Predicted to be located in mitochondrion. Used to study multiple mitochondrial dysfunctions syndrome 1. Human ortholog(s) of this gene implicated in multiple mitochondrial dysfunctions syndrome 1. Is an ortholog of human NFU1 (NFU1 iron-sulfur cluster scaffold).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_infoExperimental_modelDOID:0080133Homo sapiensPaper_evidenceWBPaper00061852
Curator_confirmedWBPerson324
Date_last_updated18 Jan 2022 00:00:00
Potential_modelDOID:0080133Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:16287)
Models_disease_assertedWBDOannot00001084
WBDOannot00001085
WBDOannot00001086
WBDOannot00001087
WBDOannot00001088
WBDOannot00001089
Molecular_infoCorresponding_CDSR10H10.1
Corresponding_CDS_historyR10H10.1:wp270
Corresponding_transcriptR10H10.1.1
Other_sequence (43)
Associated_featureWBsf228988
Experimental_infoRNAi_result (13)
Expr_patternExpr1014575
Expr1031442
Expr1155403
Expr2013255
Expr2031486
Drives_constructWBCnstr00036253
Construct_productWBCnstr00036253
WBCnstr00042900
WBCnstr00042901
WBCnstr00042902
Microarray_results (19)
Expression_cluster (104)
Interaction (49)
WBProcessWBbiopr:00000121
Map_infoMapIVPosition4.57979Error0.000279
PositivePositive_cloneR10H10Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
Reference (11)
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