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WormBase Tree Display for Gene: WBGene00009882

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Name Class

WBGene00009882SMapS_parentSequenceF49C12
IdentityVersion3
NameCGC_namevha-17
Sequence_nameF49C12.13
Molecular_nameF49C12.13
F49C12.13.1
CE37521
Other_namefus-1Paper_evidenceWBPaper00026591
Person_evidenceWBPerson539
WBPerson4071
CELE_F49C12.13Accession_evidenceNDBBX284604
Public_namevha-17
DB_infoDatabaseAceViewgene4K87
WormQTLgeneWBGene00009882
WormFluxgeneWBGene00009882
NDBlocus_tagCELE_F49C12.13
PanthergeneCAEEL|WormBase=WBGene00009882|UniProtKB=Q20591
familyPTHR12263
NCBIgene177757
RefSeqproteinNM_069235.10
SwissProtUniProtAccQ20591
TREEFAMTREEFAM_IDTF300290
UniProt_GCRPUniProtAccQ20591
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:50WBPerson1971EventImportedInitial conversion from CDS class of WS125
205 Jul 2004 16:15:45WBPerson1971Name_changeCGC_namevha-17
312 Jan 2006 15:59:17WBPerson2970EventAcquires_mergeWBGene00001504
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classvha
AlleleWBVar00275112
WBVar00431974
WBVar01500079
WBVar01498996
WBVar00931288
WBVar00931289
WBVar01498928
WBVar01500245
StrainWBStrain00022762
RNASeq_FPKM (74)
GO_annotation (16)
Ortholog (44)
Structured_descriptionConcise_descriptionvha-17 (aka 'fus-1') encodes an an ortholog of subunit e of themembrane-bound (V0) domain of vacuolar proton-translocating ATPase(V-ATPase); VHA-17, like VHA-1 and VHA-12, antagonizes EFF-1-mediatedcell fusion in hypodermal cells; VHA-17 is expressed in gut cells ofcomma stage embryos, and in excretory cell and apical membranes of gutcells at later embryonic stages; VHA-17 is found in gut granules (a typeof lysosome, expected to require acidification), and glo-1 mutantintestines fail to show punctate VHA-17; VHA-17 is required forviability, but this is at least somewhat genetically separable fromVHA-17's antifusogenic activity.Paper_evidenceWBPaper00025094
WBPaper00026591
WBPaper00026649
WBPaper00028773
WBPaper00028774
WBPaper00028775
Curator_confirmedWBPerson567
Date_last_updated19 Nov 2006 00:00:00
Automated_descriptionPredicted to enable proton-transporting ATPase activity, rotational mechanism. Involved in embryo development; embryonic body morphogenesis; and regulation of syncytium formation by plasma membrane fusion. Located in apical junction complex and apical plasma membrane. Expressed in excretory cell; hypodermal cell; and intestine. Is an ortholog of human ATP6V0E2 (ATPase H+ transporting V0 subunit e2).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
Molecular_infoCorresponding_CDSF49C12.13
Corresponding_CDS_historyF49C12.13:wp132
Corresponding_transcriptF49C12.13.1
Other_sequence (61)
Associated_featureWBsf655040
WBsf655041
WBsf228811
Experimental_infoRNAi_result (26)
Expr_patternExpr3750
Expr1024362
Expr1034309
Expr1151634
Expr2017983
Expr2036119
Drives_constructWBCnstr00031847
Construct_productWBCnstr00031847
AntibodyWBAntibody00000847
Microarray_results (20)
Expression_cluster (107)
InteractionWBInteraction000004840
WBInteraction000299408
WBInteraction000502754
WBInteraction000521887
Map_infoMapIVPosition4.16956Error0.004099
PositivePositive_cloneF49C12Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point5673
5411
Pseudo_map_position
Reference (12)
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