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WormBase Tree Display for Gene: WBGene00006920

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Name Class

WBGene00006920SMapS_parentSequenceY38F2AL
IdentityVersion1
NameCGC_namevha-11
Sequence_nameY38F2AL.3
Molecular_nameY38F2AL.3a
Y38F2AL.3a.1
CE29997
Y38F2AL.3b
CE38743
Y38F2AL.3b.1
Other_nameCELE_Y38F2AL.3Accession_evidenceNDBBX284604
Public_namevha-11
DB_infoDatabaseAceViewgene4D74
WormQTLgeneWBGene00006920
WormFluxgeneWBGene00006920
NDBlocus_tagCELE_Y38F2AL.3
PanthergeneCAEEL|WormBase=WBGene00006920|UniProtKB=Q9XXU9
familyPTHR10137
NCBIgene177017
RefSeqproteinNM_001380087.1
NM_001028280.6
SwissProtUniProtAccQ9XXU9
TREEFAMTREEFAM_IDTF314912
UniProt_GCRPUniProtAccQ9XXU9
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:43WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classvha
Allele (152)
StrainWBStrain00049354
WBStrain00051762
WBStrain00051767
RNASeq_FPKM (74)
GO_annotation (18)
Contained_in_operonCEOP4638
Ortholog (44)
Structured_descriptionConcise_descriptionvha-11 encodes, by alternative splicing, two isoforms of an ortholog ofsubunit C of the cytoplasmic (V1) domain of vacuolarproton-translocating ATPase (V-ATPase); VHA-11 is a predicted cytosolicstator (stalk) component; VHA-11 is found in dot-like structures aroundembryonic nuclei, with diffuse distribution in embryonic cytoplasm; inlater embryos (comma stage onward), VHA-11 is found in gut granules (atype of lysosome, expected to require acidification); VHA-11 ispredominantly expressed in the excretory cell and in intestinal cells inthe adult; VHA-11 is required for ovulation and embryogenesis, sincevha-11(RNAi) animals are sterile with polyploid, unmatured oocytes anddead progeny; VHA-11 is also required for normal formation of gutgranules, since vha-11(RNAi) embryonic intestines fail to stain withacridine orange; glo-1 mutant intestines fail to show punctate VHA-11;vha-11 shares an operon with vha-3; transgenic vha-11 complements anull mutation of its S. cerevisiae ortholog, VMA5.Paper_evidenceWBPaper00003195
WBPaper00004341
WBPaper00025094
WBPaper00028773
WBPaper00028774
WBPaper00028775
Curator_confirmedWBPerson324
WBPerson567
Date_last_updated19 Nov 2006 00:00:00
Automated_descriptionPredicted to enable proton-transporting ATPase activity, rotational mechanism. Involved in embryo development and ovulation. Predicted to be located in cytoplasm and membrane. Predicted to be part of vacuolar proton-transporting V-type ATPase, V1 domain. Expressed in excretory cell; hypodermis; and intestinal cell. Human ortholog(s) of this gene implicated in oral squamous cell carcinoma and stomach carcinoma. Is an ortholog of human ATP6V1C1 (ATPase H+ transporting V1 subunit C1).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:0050866Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:856)
DOID:5517Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:856)
Molecular_infoCorresponding_CDSY38F2AL.3a
Y38F2AL.3b
Corresponding_CDS_historyY38F2AL.3b:wp144
Corresponding_transcriptY38F2AL.3a.1
Y38F2AL.3b.1
Other_sequence (125)
Associated_featureWBsf667772
WBsf667773
WBsf981687
WBsf995658
WBsf995659
WBsf995660
WBsf1016884
WBsf229803
WBsf229804
WBsf229805
Experimental_infoRNAi_result (13)
Expr_patternExpr951
Expr1401
Expr1013583
Expr1032937
Expr1159566
Expr2017977
Expr2036113
Drives_constructWBCnstr00010261
AntibodyWBAntibody00000315
Microarray_results (31)
Expression_cluster (172)
Interaction (53)
Map_infoMapIVPosition-8.18629Error0.045922
PositivePositive_cloneY38F2ALInferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
Reference (14)
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