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WormBase Tree Display for Gene: WBGene00017016

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Name Class

WBGene00017016SMapS_parentSequenceD1014
IdentityVersion3
NameCGC_namesnap-1Person_evidenceWBPerson451
Sequence_nameD1014.3
Molecular_nameD1014.3a
D1014.3a.1
CE38494
D1014.3b
CE53052
D1014.3b.1
D1014.3b.2
D1014.3b.3
Other_namephi-29Person_evidenceWBPerson2582
CELE_D1014.3Accession_evidenceNDBBX284605
Public_namesnap-1
DB_infoDatabaseAceViewgene5I613
WormQTLgeneWBGene00017016
WormFluxgeneWBGene00017016
NDBlocus_tagCELE_D1014.3
PanthergeneCAEEL|WormBase=WBGene00017016|UniProtKB=Q18921
familyPTHR13768
NCBIgene179193
RefSeqproteinNM_001392555.1
NM_072698.7
TrEMBLUniProtAccA0A486WXT8
Q18921
UniProt_GCRPUniProtAccQ18921
OMIMgene611270
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:58WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
217 Mar 2005 13:54:35WBPerson2970Name_changeOther_namephi-29
307 Sep 2006 08:05:50WBPerson2970Name_changeCGC_namesnap-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsnap
Allele (39)
RNASeq_FPKM (74)
GO_annotation (12)
Contained_in_operonCEOP5180
Ortholog (48)
ParalogWBGene00013345Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00044794Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable soluble NSF attachment protein activity and syntaxin binding activity. Involved in IRE1-mediated unfolded protein response. Predicted to be located in membrane. Predicted to be part of SNARE complex. Human ortholog(s) of this gene implicated in Alzheimer's disease; Down syndrome; and developmental and epileptic encephalopathy 107. Is an ortholog of human NAPA (NSF attachment protein alpha) and NAPB (NSF attachment protein beta).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:0070393Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:15751)
DOID:10652Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:15751)
DOID:14250Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:15751)
Molecular_infoCorresponding_CDSD1014.3a
D1014.3b
Corresponding_CDS_historyD1014.3:wp142
Corresponding_transcriptD1014.3a.1
D1014.3b.1
D1014.3b.2
D1014.3b.3
Other_sequence (35)
Associated_featureWBsf646987
WBsf646988
WBsf661465
WBsf661466
WBsf981966
WBsf1000585
WBsf232064
WBsf232065
Experimental_infoRNAi_result (32)
Expr_patternExpr5609
Expr1016527
Expr1037312
Expr1147322
Expr2015937
Expr2034170
Drives_constructWBCnstr00004056
WBCnstr00027636
Construct_productWBCnstr00027636
Microarray_results (21)
Expression_cluster (101)
Interaction (85)
Map_infoMapVPosition1.04508Error0.011611
PositivePositive_cloneD1014Inferred_automaticallyFrom 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