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WormBase Tree Display for Gene: WBGene00020636

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Name Class

WBGene00020636SMapS_parentSequenceT20H4
IdentityVersion2
NameCGC_namendus-8Person_evidenceWBPerson555
Sequence_nameT20H4.5
Molecular_nameT20H4.5
T20H4.5.1
CE00832
Other_nameCELE_T20H4.5Accession_evidenceNDBBX284603
Public_namendus-8
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:03WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
216 Jan 2023 18:37:21WBPerson51134Name_changeCGC_namendus-8
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classndus
Allele (19)
RNASeq_FPKM (74)
GO_annotation (20)
Contained_in_operonCEOP3424
Ortholog (38)
Structured_descriptionConcise_descriptionT20H4.5 gene encodes a 23 kDa subunit of mitochondrial complex I that is required for oxidative phosphorylation and for resistance to volatile anesthetics; T20H4.5 is orthologous to human NADH-Ubiquinone oxidoreductase Fe-S protein 8 (NDUFS8); RNA interference screens indicate that it may be involved in longevity.Paper_evidenceWBPaper00004637
WBPaper00028429
WBPaper00026643
Curator_confirmedWBPerson324
WBPerson1823
WBPerson567
Date_last_updated15 Jun 2012 00:00:00
Automated_descriptionPredicted to enable 4 iron, 4 sulfur cluster binding activity; NADH dehydrogenase (ubiquinone) activity; and metal ion binding activity. Predicted to contribute to NADH dehydrogenase activity. Involved in mitochondrial electron transport, NADH to ubiquinone and response to xenobiotic stimulus. Located in mitochondrion. Used to study mitochondrial metabolism disease. Human ortholog(s) of this gene implicated in nuclear type mitochondrial complex I deficiency 2. Is an ortholog of human NDUFS8 (NADH:ubiquinone oxidoreductase core subunit S8).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:700Homo sapiensPaper_evidenceWBPaper00064182
Curator_confirmedWBPerson324
Date_last_updated11 Oct 2022 00:00:00
Potential_modelDOID:0112083Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7715)
Models_disease_in_annotationWBDOannot00001331
WBDOannot00001335
Molecular_infoCorresponding_CDST20H4.5
Corresponding_transcriptT20H4.5.1
Other_sequence (109)
Associated_featureWBsf651188
WBsf992965
WBsf992966
WBsf1015204
WBsf1015205
WBsf1015206
WBsf226942
WBsf226943
WBsf226944
Experimental_infoRNAi_result (20)
Expr_patternExpr1016049
Expr1038991
Expr1157229
Expr2006306
Expr2024526
Drives_constructWBCnstr00024992
Construct_productWBCnstr00024992
Microarray_results (18)
Expression_cluster (116)
Interaction (131)
Map_infoMapIIIPosition-0.767593
PositivePositive_cloneT20H4Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00003662
WBPaper00005928
WBPaper00028429
WBPaper00034662
WBPaper00038491
WBPaper00055090
WBPaper00056909
WBPaper00064182
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