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WormBase Tree Display for Gene: WBGene00015327

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Name Class

WBGene00015327SMapS_parentSequenceC02B10
IdentityVersion2
NameCGC_namesnpn-1Person_evidenceWBPerson253
Sequence_nameC02B10.2
Molecular_nameC02B10.2
C02B10.2.1
CE24776
Other_nameCELE_C02B10.2Accession_evidenceNDBBX284604
Public_namesnpn-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:55WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
231 Aug 2012 11:56:39WBPerson2970Name_changeCGC_namesnpn-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsnpn
AlleleWBVar00424621
WBVar00908698
WBVar01794681
WBVar00250855
WBVar01499754
WBVar01499242
WBVar01499633
WBVar01481837
WBVar01500245
RNASeq_FPKM (74)
GO_annotation (15)
Ortholog (30)
Structured_descriptionAutomated_descriptionPredicted to enable SNARE binding activity. Involved in endosomal transport and positive regulation of intracellular protein transport. Predicted to be located in synaptic vesicle. Predicted to be part of BLOC-1 complex and BORC complex. Used to study Hermansky-Pudlak syndrome. Is an ortholog of human SNAPIN (SNAP associated 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:3753Homo sapiensPaper_evidenceWBPaper00041456
Accession_evidenceOMIM614171
Curator_confirmedWBPerson324
Date_last_updated17 Oct 2018 00:00:00
Disease_relevanceDefective formation of lysosome-related organelles (LROs) underlies the human disease Hermansky-Pudlak syndrome (HPS); the nine genes currently implicated in causing HPS encode subunits of the AP-3, BLOC-1, BLOC-2, or BLOC-3 complexes; BLOC1 is required for normal biogenesis of specialized organelles of the endosomal-lysosomal system, such as melanosomes and platelet dense granules; C. elegans glo-2 and snpn-1 encode Pallidin and Snapin, which are BLOC-1 subunit homologs, respectively; studies in elegans show that snpn-1 and glo-2 function in trafficking to, and biogenesis of gut granules (gut granules are intestinal cell-specific LROs); snpn-1, but not glo-2 interacts with dsbn-1, which is similar to human dysbindin (DTNBP1), a mammalian BLOC-1 subunit; this system provides an in vivo model to study the genetics and interactions of BLOC1 subunits.Homo sapiensPaper_evidenceWBPaper00041456
Accession_evidenceOMIM614171
607007
Curator_confirmedWBPerson324
Date_last_updated19 Feb 2014 00:00:00
Models_disease_assertedWBDOannot00000097
Molecular_info (4)
Experimental_infoRNAi_resultWBRNAi00008198Inferred_automaticallyRNAi_primary
WBRNAi00028325Inferred_automaticallyRNAi_primary
WBRNAi00009965Inferred_automaticallyRNAi_primary
WBRNAi00039386Inferred_automaticallyRNAi_primary
Expr_patternExpr1019539
Expr1036564
Expr1143503
Expr2015964
Expr2034199
Drives_constructWBCnstr00017656
WBCnstr00028932
Construct_productWBCnstr00017656
WBCnstr00028932
Microarray_results (20)
Expression_cluster (122)
Interaction (60)
Map_info (3)
ReferenceWBPaper00038491
WBPaper00041456
WBPaper00042250
WBPaper00052655
WBPaper00052935
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