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WormBase Tree Display for Gene: WBGene00018853

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Name Class

WBGene00018853SMapS_parentSequenceF55A4
IdentityVersion2
NameCGC_namesec-22Person_evidenceWBPerson3132
Sequence_nameF55A4.1
Molecular_nameF55A4.1
F55A4.1.1
CE19895
Other_nameCELE_F55A4.1Accession_evidenceNDBBX284606
Public_namesec-22
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:00WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
226 Mar 2010 11:10:22WBPerson2970Name_changeCGC_namesec-22
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsec
Allele (23)
StrainWBStrain00001453
WBStrain00002575
WBStrain00032937
RNASeq_FPKM (74)
GO_annotation (25)
Ortholog (34)
ParalogWBGene00004897Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00004898Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00004899Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00007200Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00014084Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00015164Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00022077Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00044062Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable SNAP receptor activity. Involved in IRE1-mediated unfolded protein response. Predicted to be located in endoplasmic reticulum-Golgi intermediate compartment and organelle membrane. Predicted to be part of SNARE complex. Expressed in somatic cell and tail. Used to study Parkinson's disease. Is an ortholog of human SEC22B (SEC22 homolog B, vesicle trafficking protein).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:14330Homo sapiensPaper_evidenceWBPaper00031384
Curator_confirmedWBPerson324
Date_last_updated24 Jul 2013 00:00:00
Disease_relevanceIn an elegans model of Parkinson''s disease, where human alpha-synuclein was overexpressed, RNA interference studies showed that the elegans sec-22/SEC22A (homolog of yeast sec22p vesicle trafficking protein), significantly protected against age- and dose-dependent degeneration in the dopamine neurons of transgenic worms; such models allow the identification of human modifier proteins of alpha-synuclein dependent misfolding and neurodegeneration, these proteins may also be new potential targets for therapeutic intervention.Homo sapiensPaper_evidenceWBPaper00031384
Accession_evidenceOMIM612442
Curator_confirmedWBPerson324
Date_last_updated24 Jul 2013 00:00:00
Models_disease_in_annotationWBDOannot00000216
Molecular_infoCorresponding_CDSF55A4.1
Corresponding_transcriptF55A4.1.1
Other_sequence (41)
Associated_featureWBsf647814
WBsf235303
WBsf235304
Experimental_infoRNAi_resultWBRNAi00076480Inferred_automaticallyRNAi_primary
WBRNAi00110503Inferred_automaticallyRNAi_primary
WBRNAi00032843Inferred_automaticallyRNAi_primary
WBRNAi00015681Inferred_automaticallyRNAi_primary
WBRNAi00048433Inferred_automaticallyRNAi_primary
WBRNAi00110527Inferred_automaticallyRNAi_primary
WBRNAi00110515Inferred_automaticallyRNAi_primary
Expr_patternChronogram1322
Chronogram1425
Expr6194
Expr13362
Expr1022198
Expr1038135
Expr1152220
Expr2015712
Expr2033944
Drives_constructWBCnstr00004232
WBCnstr00004233
WBCnstr00026240
WBCnstr00039343
Construct_productWBCnstr00006220
WBCnstr00006227
WBCnstr00026240
WBCnstr00039343
Microarray_results (19)
Expression_cluster (141)
Interaction (51)
Map_infoMapXPosition-18.7988Error0.009491
PositivePositive_cloneF55A4Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00031384
WBPaper00038491
WBPaper00042644
WBPaper00043668
WBPaper00050534
WBPaper00055090
WBPaper00061547
WBPaper00066137
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