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WormBase Tree Display for Gene: WBGene00004898

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Name Class

WBGene00004898EvidenceAccession_evidenceEMBLAF239889
SMapS_parentSequenceF23H12
IdentityVersion1
NameCGC_namesnb-2
Sequence_nameF23H12.1
Molecular_nameF23H12.1
F23H12.1.1
CE42855
Other_nameCELE_F23H12.1Accession_evidenceNDBBX284605
Public_namesnb-2
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:36WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsnb
Allele (34)
RNASeq_FPKM (74)
GO_annotation00065794
00065795
00065796
00065797
00065798
00065799
00113306
00113307
Contained_in_operonCEOP5518
Ortholog (30)
ParalogWBGene00004897Caenorhabditis elegansFrom_analysisInparanoid_8
Panther
WormBase-Compara
WBGene00022077Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00004899Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00007200Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00014084Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00015164Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00018853Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00044062Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable SNAP receptor activity and syntaxin binding activity. Predicted to be involved in vesicle fusion. Predicted to be located in plasma membrane. Predicted to be part of SNARE complex. Human ortholog(s) of this gene implicated in congenital myasthenic syndrome and spastic ataxia 1. Is an ortholog of human VAMP1 (vesicle associated membrane protein 1) and VAMP3 (vesicle associated membrane protein 3).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:0050772Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12642)
DOID:3635Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12642)
Molecular_infoCorresponding_CDSF23H12.1
Corresponding_CDS_historyF23H12.1:wp51
F23H12.1:wp193
Corresponding_transcriptF23H12.1.1
Other_sequenceAF239889
Associated_featureWBsf234667
WBsf234668
Experimental_infoRNAi_resultWBRNAi00091335Inferred_automaticallyRNAi_primary
WBRNAi00065642Inferred_automaticallyRNAi_primary
WBRNAi00031339Inferred_automaticallyRNAi_primary
WBRNAi00045449Inferred_automaticallyRNAi_primary
WBRNAi00013836Inferred_automaticallyRNAi_primary
WBRNAi00045450Inferred_automaticallyRNAi_primary
Expr_patternExpr1015814
Expr1149368
Expr2015940
Expr2034173
Drives_constructWBCnstr00035336
Construct_productWBCnstr00035336
Microarray_results (25)
Expression_cluster (145)
Interaction (22)
Map_infoMapVPosition4.0055Error0.001281
PositivePositive_cloneF23H12Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
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