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WormBase Tree Display for Gene: WBGene00016960

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Name Class

WBGene00016960SMapS_parentSequenceC56C10
IdentityVersion2
NameCGC_namevps-33.2Paper_evidenceWBPaper00031805
Person_evidenceWBPerson426
Sequence_nameC56C10.1
Molecular_nameC56C10.1
C56C10.1.1
CE30636
Other_nameCELE_C56C10.1Accession_evidenceNDBBX284602
Public_namevps-33.2
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:58WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
215 Mar 2007 17:00:31WBPerson2970Name_changeCGC_namevps-33.2
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classvps
AlleleWBVar01499702
WBVar01498435
WBVar00739092
WBVar00739093
WBVar00739094
WBVar00739095
WBVar00368537
WBVar00739096
WBVar00368538
WBVar00368539
WBVar00739097
WBVar00368540
WBVar00739098
WBVar00368541
WBVar00739099
WBVar00739100
WBVar00249563
WBVar00739101
WBVar00739102
WBVar02147747
WBVar02147748
WBVar02147750
WBVar02147751
WBVar01438214
WBVar01438215
WBVar01438216
WBVar01240503
WBVar01666158
WBVar02033361
WBVar00602313
WBVar01783853
In_clusterconserved_miRNA_siRNA_cluster
RNASeq_FPKM (74)
GO_annotation (18)
Ortholog (41)
ParalogWBGene00006757Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00009654Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00015130Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00016643Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00020298Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionAutomated_descriptionInvolved in spermatocyte division. Predicted to be located in lysosome. Predicted to be part of CORVET complex. Expressed in intestine; pharynx; and spermatheca. Used to study ARC syndrome. Human ortholog(s) of this gene implicated in several diseases, including arthrogryposis multiplex congenita; arthrogryposis, renal dysfunction, and cholestasis 1; and progressive familial intrahepatic cholestasis. Is an ortholog of human VPS33B (VPS33B late endosome and lysosome associated).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:0050763Homo sapiensPaper_evidenceWBPaper00032464
Curator_confirmedWBPerson38202
Date_last_updated30 May 2018 00:00:00
Potential_modelDOID:557Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12712)
DOID:0111353Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12712)
DOID:0070221Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12712)
DOID:13580Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12712)
DOID:0080954Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12712)
Models_disease_in_annotationWBDOannot00000535
Molecular_infoCorresponding_CDSC56C10.1
Corresponding_transcriptC56C10.1.1
Other_sequenceTcol_isotig02052
CR04921
Hbac_isotig05781
Dviv_isotig29676
Oden_isotig27960
CRC09241_1
Acan_isotig14752
Associated_featureWBsf644309
WBsf657701
WBsf221470
Experimental_infoRNAi_result (14)
Expr_patternExpr12007
Expr13085
Expr1012862
Expr1037275
Expr1147239
Expr2018024
Expr2036161
Drives_constructWBCnstr00019957
WBCnstr00027677
WBCnstr00038575
Construct_productWBCnstr00019957
WBCnstr00027677
WBCnstr00038575
Microarray_results (22)
Expression_cluster (118)
Interaction (86)
Map_infoMapIIPosition-0.080891Error0.00486
PositivePositive_cloneC56C10Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00031805
WBPaper00032464
WBPaper00038491
WBPaper00050040
WBPaper00055090
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