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WormBase Tree Display for Gene: WBGene00000210

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Name Class

WBGene00000210SMapS_parentSequenceC53B7
IdentityVersion1
NameCGC_nameasg-2Person_evidenceWBPerson284
Sequence_nameC53B7.4
Molecular_nameC53B7.4
C53B7.4.1
CE06974
Other_nameCELE_C53B7.4Accession_evidenceNDBBX284606
Public_nameasg-2
DB_infoDatabaseAceViewgeneXH461
WormQTLgeneWBGene00000210
WormFluxgeneWBGene00000210
NDBlocus_tagCELE_C53B7.4
PanthergeneCAEEL|WormBase=WBGene00000210|UniProtKB=Q18803
familyPTHR12386
NCBIgene180956
RefSeqproteinNM_076751.8
SwissProtUniProtAccQ18803
TREEFAMTREEFAM_IDTF313978
UniProt_GCRPUniProtAccQ18803
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:20WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classasg
Allele (17)
StrainWBStrain00033109
RNASeq_FPKM (74)
GO_annotation (16)
Ortholog (39)
ParalogWBGene00000209Caenorhabditis elegansFrom_analysisInparanoid_8
Panther
WormBase-Compara
Structured_descriptionConcise_descriptionasg-2 encodes a homolog of subunit G of the membrane-bound F0 proton channel portion of ATP synthase (mitochondrial respiratory chain [MRC] complex V); asg-2 activity is required for growth at a normally high rate and for normal osmoregulation; in addition, asg-2 activity is required for response to hermaphrodite contact, the first step in a series of stereotypical male mating behaviors; an ASG-2::GFP fusion localizes to mitochondria and to cilia of the male-specific CEM neurons.Paper_evidenceWBPaper00024944
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated16 Jan 2007 00:00:00
Automated_descriptionPredicted to enable proton transmembrane transporter activity. Predicted to contribute to proton-transporting ATP synthase activity, rotational mechanism. Predicted to be involved in proton motive force-driven ATP synthesis. Located in mitochondrion and non-motile cilium. Human ortholog(s) of this gene implicated in Alzheimer's disease. Is an ortholog of human ATP5MG (ATP synthase membrane subunit g).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:10652Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:14247)
Molecular_infoCorresponding_CDSC53B7.4
Corresponding_transcriptC53B7.4.1
Other_sequence (34)
Associated_featureWBsf648265
WBsf1005656
WBsf235874
WBsf235875
Experimental_infoRNAi_result (15)
Expr_patternExpr1023761
Expr1030129
Expr1147043
Expr2009450
Expr2027687
Drives_constructWBCnstr00037662
Construct_productWBCnstr00037662
Microarray_results (20)
Expression_cluster (172)
Interaction (73)
Map_infoMapXPosition-2.33933Error0.004066
PositivePositive_cloneC53B7Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00024944
WBPaper00025859
WBPaper00028999
WBPaper00033540
WBPaper00038491
WBPaper00049828
WBPaper00055090
WBPaper00061852
RemarkSequence connection from [Iino Y]
Map 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