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WormBase Tree Display for Gene: WBGene00006798

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Name Class

WBGene00006798SMapS_parentSequenceF56A8
IdentityVersion2
NameCGC_nameunc-64Person_evidenceWBPerson261
Sequence_nameF56A8.7
Molecular_nameF56A8.7a
F56A8.7a.1
CE16127
F56A8.7b
CE28035
F56A8.7a.2
F56A8.7b.1
Other_namesyx-1Person_evidenceWBPerson3132
CELE_F56A8.7Accession_evidenceNDBBX284603
Public_nameunc-64
DB_infoDatabaseAceViewgene3O371
WormQTLgeneWBGene00006798
WormFluxgeneWBGene00006798
NDBlocus_tagCELE_F56A8.7
PanthergeneCAEEL|WormBase=WBGene00006798|UniProtKB=O16000
familyPTHR19957
NCBIgene176743
RefSeqproteinNM_001027443.6
NM_001379980.1
SwissProtUniProtAccO16000
UniProt_GCRPUniProtAccO16000
OMIMgene600876
601485
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:43WBPerson1971EventImportedInitial conversion from geneace
216 Apr 2010 14:03:06WBPerson2970Name_changeOther_namesyx-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classunc
Reference_alleleWBVar00143062
Allele (105)
Legacy_informatione246 : sluggish will move either forward or backward if prodded but almost immediately jams up; partially lannate resistant; healthy. ES2 ME0. NA1.
See also e246
[C.elegansII] e246 : sluggish, will move either forward or backward if prodded but almost immediately jams up; Ric; healthy; elevated acetylcholine levels. ES2 ME0. OA>1 (some alleles lead to severe paralysis). Cloned: encodes predicted syntaxin homolog. [Brenner 1974; Nguyen et al. 1995; NM; RM; TN]
[Ogawa H, Hosono R] e246 is A248V, in predicted 291aa syntaxin homologue, 63% identical to human syntaxin. unc-64::GFP expressed extensively in neurons. Predicted gene F56A8.7
StrainWBStrain00026467
WBStrain00029044
WBStrain00029049
WBStrain00030888
WBStrain00004366
WBStrain00004134
WBStrain00007239
WBStrain00055180
RNASeq_FPKM (74)
GO_annotation (41)
Ortholog (43)
ParalogWBGene00006371Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00006372Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00006373Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00006374Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00012150Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00009478Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00022534Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionunc-64 encodes syntaxin, a plasma membrane receptor for intracellular vesicles that is orthologous to vertebrate syntaxin 1A (OMIM:186590) and Drosophila Syx1A; UNC-64 is required for normal locomotion and possibly also for insulin secretion; as an essential component of the core synaptic vesicle fusion machinery, UNC-64 interacts with UNC-13, a diacylglycerol-binding protein, and SNB-1/synaptobrevin; UNC-64 trafficking from the endoplasmic reticulum to the plasma membrane is mediated by UNC-18, an SM (Sec1, Munc18) family member; unc-64 mutations can be suppressed by mutations in slo-1, a calcium-activated potassium channel; UNC-64 is expressed ubiquitously in the nervous system and in secretory cells such as the vulval uv1 cell and the excretory gland cells.Paper_evidenceWBPaper00003101
WBPaper00005015
WBPaper00005528
WBPaper00006124
WBPaper00031990
Curator_confirmedWBPerson1843
Date_last_updated04 Nov 2008 00:00:00
Automated_descriptionEnables protein-folding chaperone binding activity. Involved in several processes, including chemical synaptic transmission; positive regulation of anterior/posterior axon guidance; and ventral cord development. Located in axon; basolateral plasma membrane; and somatodendritic compartment. Expressed in several structures, including excretory gland cell; hermaphrodite gonad; intestine; nervous system; and rectal gland cell. Human ortholog(s) of this gene implicated in several diseases, including Creutzfeldt-Jakob disease; Hirschsprung's disease; and generalized epilepsy with febrile seizures plus 9. Is an ortholog of human STX1A (syntaxin 1A).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:11949Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11433)
DOID:10487Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11433)
DOID:0111301Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18539)
DOID:0060774Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11438)
Molecular_infoCorresponding_CDSF56A8.7a
F56A8.7b
Corresponding_transcriptF56A8.7a.1
F56A8.7a.2
F56A8.7b.1
Other_sequence (58)
Associated_featureWBsf659704
WBsf659705
WBsf659706
WBsf718014
WBsf994847
WBsf225978
WBsf225979
Experimental_infoRNAi_result (13)
Expr_pattern (14)
Drives_construct (15)
Construct_product (13)
AntibodyWBAntibody00000180
Microarray_results (28)
Expression_cluster (160)
Interaction (203)
Map_infoMapIIIPosition21.1995Error0.007471
Well_ordered
PositiveInside_rearreDf2
eDp6
ctDf2
Positive_cloneB0502
C26A4
F56A8Inferred_automaticallyFrom sequence, transcript, pseudogene data
NegativeOutside_rearrtDf10
Mapping_data (3)
Landmark_gene
Reference (197)
RemarkData extracted from Ogawa et al. (1998)
MethodGene