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WormBase Tree Display for Gene: WBGene00013804

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Name Class

WBGene00013804SMapS_parentSequenceY116A8C
IdentityVersion1
NameSequence_nameY116A8C.27
Molecular_nameY116A8C.27a
Y116A8C.27a.1
CE37421
Y116A8C.27b
CE44714
Y116A8C.27b.1
Other_nameCELE_Y116A8C.27Accession_evidenceNDBBX284604
Public_nameY116A8C.27
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:55WBPerson1971EventImportedInitial conversion from CDS class of WS125
StatusLive
Gene_infoBiotypeSO:0001217
Allele (176)
RNASeq_FPKM (74)
GO_annotation00007383
00007384
00099636
00099637
00120580
Contained_in_operonCEOP4596
Ortholog (37)
Structured_descriptionAutomated_descriptionPredicted to be involved in mitochondrial proton-transporting ATP synthase complex assembly. Predicted to be located in mitochondrion. Human ortholog(s) of this gene implicated in mitochondrial complex V (ATP synthase) deficiency nuclear type 1. Is an ortholog of human ATPAF2 (ATP synthase mitochondrial F1 complex assembly factor 2).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:0050768Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18802)
Molecular_infoCorresponding_CDSY116A8C.27a
Y116A8C.27b
Corresponding_CDS_historyY116A8C.27:wp131
Corresponding_transcriptY116A8C.27a.1
Y116A8C.27b.1
Other_sequence (62)
Associated_featureWBsf668580
Experimental_infoRNAi_resultWBRNAi00055446Inferred_automaticallyRNAi_primary
WBRNAi00055444Inferred_automaticallyRNAi_primary
Expr_patternExpr1028627
Expr1036179
Expr1158956
Expr2007047
Expr2025274
Microarray_results (21)
Expression_cluster (93)
Interaction (39)
Map_infoPositivePositive_cloneY116A8CInferred_automaticallyFrom sequence, transcript, pseudogene data
Interpolated_map_positionIV16.1363
ReferenceWBPaper00038491
WBPaper00055090
MethodGene