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WormBase Tree Display for Gene: WBGene00004913

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Name Class

WBGene00004913SMapS_parentSequenceY38C1BA
IdentityVersion1
NameCGC_namesnn-1
Sequence_nameY38C1BA.2
Molecular_nameY38C1BA.2a
Y38C1BA.2a.1
CE28520
Y38C1BA.2b
CE31645
Y38C1BA.2a.2
Y38C1BA.2a.3
Y38C1BA.2a.4
Y38C1BA.2b.1
Other_namesynAccession_evidenceEMBLAF192746
CELE_Y38C1BA.2Accession_evidenceNDBBX284604
Public_namesnn-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:36WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsnn
Allele (260)
RNASeq_FPKM (74)
GO_annotation (13)
Ortholog (42)
Structured_descriptionConcise_descriptionsnn-1 encodes the C. elegans synapsin ortholog; snn-1 is required for proper synaptic function, as loss of snn-1 results in a decrease in acetylcholine release; SNN-1::GFP reporters are expressed in neurons and exhibit patterns consistent with localization to vesicles in presynaptic regions.Paper_evidenceWBPaper00026667
WBPaper00028808
Curator_confirmedWBPerson1843
Date_last_updated03 Sep 2010 00:00:00
Automated_descriptionPredicted to enable ATP binding activity. Involved in neuromuscular synaptic transmission. Located in presynaptic periactive zone. Expressed in epithelial cell and nervous system. Human ortholog(s) of this gene implicated in several diseases, including X-linked epilepsy with variable learning disabilities and behavior disorders; major depressive disorder; and non-syndromic X-linked intellectual disability 50. Is an ortholog of human SYN3 (synapsin III).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:0112029Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11494)
DOID:1470Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11494)
DOID:0112122Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11494)
DOID:5419Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11495)
Molecular_infoCorresponding_CDSY38C1BA.2a
Y38C1BA.2b
Corresponding_transcriptY38C1BA.2a.1
Y38C1BA.2a.2
Y38C1BA.2a.3
Y38C1BA.2a.4
Y38C1BA.2b.1
Other_sequenceOden_isotig23771
CBC06607_1
Oden_isotig28596
Dviv_isotig34656
HBC23627_1
EX910972.1
Associated_featureWBsf716770
WBsf995542
WBsf1016792
WBsf229783
Experimental_infoRNAi_result (22)
Expr_patternExpr3562
Expr4962
Expr4972
Expr15242
Expr1019671
Expr1159519
Expr2015955
Expr2034190
Construct_productWBCnstr00005438
WBCnstr00011486
WBCnstr00012371
WBCnstr00012381
WBCnstr00014588
WBCnstr00017095
WBCnstr00021852
Microarray_results (32)
Expression_cluster (121)
Interaction (38)
Map_infoMapIVPosition-15.9139Error0.054711
PositivePositive_cloneY38C1BAInferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
Reference (12)
RemarkSequence connection from [Kao T, Greengard P]
Map 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