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WormBase Tree Display for Gene: WBGene00003772

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Name Class

WBGene00003772EvidenceAuthor_evidenceHaklai-Toper L
SMapS_parentSequenceF20B10
IdentityVersion1
NameCGC_namenlr-1
Sequence_nameF20B10.1
Molecular_nameF20B10.1
F20B10.1.1
CE40647
Other_nameCELE_F20B10.1Accession_evidenceNDBBX284604
Public_namenlr-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:32WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classnlr
AlleleWBVar00250996
WBVar01499892
WBVar01500079
WBVar01731280
WBVar01498811
WBVar01498996
WBVar01702987
WBVar01482437
WBVar01498636
WBVar01499925
WBVar01967137
WBVar00437362
WBVar01967138
WBVar00437363
WBVar00437364
WBVar01967139
WBVar00437365
WBVar00947214
WBVar00947215
WBVar00437366
WBVar00947216
WBVar01795630
WBVar00437367
WBVar01795631
WBVar00947217
WBVar00437368
WBVar00437369
WBVar01795632
WBVar00947218
WBVar01795633
WBVar00437370
WBVar00947219
WBVar00947220
WBVar00947221
WBVar00947222
WBVar00947223
WBVar00947224
WBVar02121218
WBVar00947225
WBVar00947226
WBVar00947227
WBVar00947228
WBVar00947229
WBVar00947230
WBVar00947231
WBVar00947232
WBVar02122146
WBVar00947233
WBVar00947234
WBVar00947235
WBVar00947236
WBVar00947237
WBVar01498307
WBVar00947238
WBVar00947239
WBVar00947240
WBVar01498310
WBVar01498869
WBVar02120508
WBVar02124014
WBVar02121623
WBVar02123095
WBVar02120706
WBVar00192352
WBVar00192353
WBVar02124210
WBVar02046054
WBVar02124966
WBVar01498735
WBVar02123512
WBVar01498569
WBVar01498754
WBVar02037203
WBVar02037204
WBVar01498576
WBVar01498581
WBVar01859134
WBVar01859135
WBVar02134792
WBVar01500245
WBVar01498775
WBVar01498777
WBVar01498779
StrainWBStrain00036730
RNASeq_FPKM (74)
GO_annotation (13)
Ortholog (47)
Paralog (49)
Structured_descriptionAutomated_descriptionEnables actin filament binding activity and gap junction channel activity. Involved in positive regulation of gap junction assembly and positive regulation of pharyngeal pumping. Located in gap junction. Expressed in RIS; pharyngeal gland cell; and pharyngeal muscle cell. Human ortholog(s) of this gene implicated in several diseases, including Pitt-Hopkins syndrome; autistic disorder; and communication disorder (multiple). Is an ortholog of human CNTNAP5 (contactin associated protein family member 5).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_model (15)
Molecular_infoCorresponding_CDSF20B10.1
Corresponding_CDS_historyF20B10.1:wp169
Corresponding_transcriptF20B10.1.1
Other_sequenceJI165112.1
Acan_isotig04777
EY458672.1
Dviv_isotig19784
JI247685.1
Dviv_isotig19785
MHC00101_1
MH05847
EY460391.1
MC03680
EY466247.1
MCC03125_1
MCC02391_1
MC03146
Acan_isotig04778
EY470001.1
MH02290
ACC08911_1
ACC26322_1
MHC02522_1
Associated_feature (18)
Experimental_infoRNAi_resultWBRNAi00045068Inferred_automaticallyRNAi_primary
WBRNAi00031154Inferred_automaticallyRNAi_primary
WBRNAi00045067Inferred_automaticallyRNAi_primary
WBRNAi00013592Inferred_automaticallyRNAi_primary
WBRNAi00115343Inferred_automaticallyRNAi_primary
WBRNAi00001494Inferred_automaticallyRNAi_primary
WBRNAi00013593Inferred_automaticallyRNAi_primary
WBRNAi00045069Inferred_automaticallyRNAi_primary
Expr_patternExpr5798
Expr9161
Expr1024841
Expr1031762
Expr1149023
Expr2014327
Expr2032568
Drives_constructWBCnstr00004190
WBCnstr00013758
WBCnstr00035876
WBCnstr00038180
Construct_productWBCnstr00035876
Microarray_results (22)
Expression_cluster (189)
Interaction (15)
Map_infoMapIVPosition5.76995Error0.010598
PositivePositive_cloneF20B10Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point5514
5519
4583
Pseudo_map_position
ReferenceWBPaper00013424
WBPaper00018360
WBPaper00019572
WBPaper00037763
WBPaper00038491
WBPaper00043312
WBPaper00055090
WBPaper00060680
WBPaper00062491
WBPaper00065331
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