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WormBase Tree Display for Gene: WBGene00007799

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Name Class

WBGene00007799SMapS_parentSequenceC29A12
IdentityVersion4
NameCGC_namenrx-1Person_evidenceWBPerson508
Sequence_nameC29A12.4
Molecular_nameC29A12.4a
C29A12.4a.1
CE46835
C29A12.4b
CE46888
C29A12.4c
CE45301
C29A12.4d
CE45317
C29A12.4e
CE20534
C29A12.4f
CE45797
C29A12.4g
CE46812
C29A12.4h
CE46590
C29A12.4i
CE41552
C29A12.4j
CE47013
C29A12.4k
CE47593
C29A12.4l
CE47540
C29A12.4m
CE48414
C29A12.4b.1
C29A12.4c.1
C29A12.4d.1
C29A12.4e.1
C29A12.4f.1
C29A12.4g.1
C29A12.4h.1
C29A12.4i.1
C29A12.4j.1
C29A12.4k.1
C29A12.4l.1
C29A12.4m.1
Other_nameCELE_C29A12.4Accession_evidenceNDBBX284605
Public_namenrx-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:48WBPerson1971EventImportedInitial conversion from CDS class of WS125
218 Feb 2005 12:07:44WBPerson2970Name_changeCGC_namenrx-1
303 Mar 2005 11:35:24WBPerson2970EventAcquires_mergeWBGene00003817
421 Jan 2011 10:43:00WBPerson4025EventAcquires_mergeWBGene00050888
Acquires_mergeWBGene00003817
WBGene00050888
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classnrx
Allele (284)
StrainWBStrain00034059
WBStrain00035064
WBStrain00036581
RNASeq_FPKM (74)
GO_annotation00005188
00005189
00023933
Ortholog (45)
Paralog (48)
Structured_descriptionConcise_descriptionnrx-1 encodes the C. elegans ortholog of neurexins, presynaptic transmembrane neural adhesion molecules that contain extracellular laminin and EGF domains and play a critical role in synaptic development; genetic analyses suggest that nrx-1 may play a role in regulation of adult lifespan; nrx-1 expression is controlled by daf-2 and daf-16.Paper_evidenceWBPaper00030810
Curator_confirmedWBPerson1843
Date_last_updated28 Jan 2009 00:00:00
Automated_descriptionInvolved in negative regulation of receptor clustering. Located in presynaptic active zone. Expressed in GABAergic neurons; cholinergic neurons; nervous system; and ventral cord neurons. Used to study autism spectrum disorder. Human ortholog(s) of this gene implicated in Pitt-Hopkins-like syndrome 2. Is an ortholog of human NRXN1 (neurexin 1) and NRXN3 (neurexin 3).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:0060041Homo sapiensPaper_evidenceWBPaper00041363
WBPaper00048837
Curator_confirmedWBPerson324
Date_last_updated09 Feb 2018 00:00:00
Potential_modelDOID:0111332Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8008)
Disease_relevanceAbnormalities in the genes encoding human Neuroligins (NLGN1,NLGN2, NLGN3, NLGN4) and Neurexins (NRXN1) are associated with Autism spectrum disorders; mutations in the elegans neurexin (nrx-1) suppress neuroligin (nlg-1) defects; nrx-1 is involved in sensory functions and adult life span and along with nrx-1 mediates a retrograde synaptic signal that inhibits neurotransmitter release at neuromuscular junctions.Homo sapiensPaper_evidenceWBPaper00028987
WBPaper00042136
Curator_confirmedWBPerson324
Date_last_updated22 Apr 2013 00:00:00
Models_disease_in_annotationWBDOannot00000165
Models_disease_assertedWBDOannot00000476
Molecular_infoCorresponding_CDS (13)
Corresponding_CDS_historyC29A12.4:wp20
C29A12.4a:wp229
C29A12.4b:wp229
C29A12.4g:wp229
C29A12.4h:wp229
Corresponding_transcript (13)
Other_sequence (17)
Associated_feature (30)
Experimental_infoRNAi_resultWBRNAi00041440Inferred_automaticallyRNAi_primary
WBRNAi00080988Inferred_automaticallyRNAi_primary
WBRNAi00011320Inferred_automaticallyRNAi_primary
WBRNAi00029309Inferred_automaticallyRNAi_primary
WBRNAi00080991Inferred_automaticallyRNAi_primary
WBRNAi00099062Inferred_automaticallyRNAi_primary
Expr_pattern (13)
Drives_constructWBCnstr00013755
WBCnstr00017468
WBCnstr00020790
WBCnstr00023198
WBCnstr00040466
WBCnstr00041192
Construct_productWBCnstr00013755
WBCnstr00013756
WBCnstr00014838
WBCnstr00020409
WBCnstr00020790
WBCnstr00023198
WBCnstr00040465
WBCnstr00040466
Regulate_expr_clusterWBPaper00053023:nrx-1(tm1961);nlg-1(ok259)_downregulated
WBPaper00053023:nrx-1(tm1961);nlg-1(ok259)_upregulated
WBPaper00053023:nrx-1(tm1961)_downregulated
WBPaper00053023:nrx-1(tm1961)_upregulated
Microarray_results (47)
Expression_cluster (185)
Interaction (19)
Map_infoMapVPosition2.82231Error0.001163
PositivePositive_cloneC29A12Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point5089
Pseudo_map_position
Reference (40)
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