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WormBase Tree Display for Gene: WBGene00006743

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Name Class

WBGene00006743SMapS_parentSequenceCHROMOSOME_X
IdentityVersion1
NameCGC_nameunc-3Person_evidenceWBPerson261
Sequence_nameY16B4A.1
Molecular_nameY16B4A.1
Y16B4A.1.1
CE29366
Other_nameCELE_Y16B4A.1Accession_evidenceNDBBX284606
Public_nameunc-3
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:41WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classunc
Reference_alleleWBVar00142996
Allele (232)
Legacy_informatione151 : weak coiler tends to coil tail active; very disorganized ventral nerve cord; mutant focus in ABp descendants; ES3 ME1. Similar phenotype in e151/Df. NA4 (e54 (weaker allele) e95 etc.).
[C.elegansII] e151 : weak coiler tends to coil, tail active, good head movement; very disorganized ventral nerve cord; mosaic analysis indicates mutant focus in ventral cord motor neurons. Similar phenotype ine151/Df. ES3 ME1.OA>5: e54 (weaker allele), e95, mn419, p1001 etc. Cloned: polymorphisms identified in mn419 and derivatives (cosmid F42D1). [Brenner 1974; Herman and Kari 1987; NG; SP]
StrainWBStrain00023812
WBStrain00023947
WBStrain00026971
WBStrain00027004
WBStrain00027373
WBStrain00027376
WBStrain00029078
WBStrain00029632
WBStrain00029635
WBStrain00029636
WBStrain00029770
WBStrain00030773
WBStrain00030774
WBStrain00030800
WBStrain00030840
WBStrain00031247
WBStrain00033501
WBStrain00034123
WBStrain00034124
WBStrain00034129
WBStrain00034130
WBStrain00034131
WBStrain00034132
WBStrain00034133
WBStrain00034135
WBStrain00034136
WBStrain00034137
WBStrain00034138
WBStrain00034157
WBStrain00034158
WBStrain00034159
WBStrain00034160
WBStrain00034161
WBStrain00034162
WBStrain00034163
WBStrain00034164
WBStrain00034165
WBStrain00034166
WBStrain00034167
WBStrain00034168
WBStrain00034169
WBStrain00034170
WBStrain00034171
WBStrain00034172
WBStrain00034173
WBStrain00034174
WBStrain00034175
WBStrain00034176
WBStrain00034177
WBStrain00034178
WBStrain00034179
WBStrain00034180
WBStrain00034200
WBStrain00034217
WBStrain00034218
WBStrain00034222
WBStrain00034223
WBStrain00034225
WBStrain00034230
WBStrain00034255
WBStrain00034309
WBStrain00034327
WBStrain00034333
WBStrain00034390
WBStrain00034395
WBStrain00034396
WBStrain00034473
WBStrain00000060
WBStrain00000292
WBStrain00004111
WBStrain00004959
WBStrain00004966
WBStrain00004967
WBStrain00004968
WBStrain00004971
WBStrain00004972
WBStrain00004973
WBStrain00004977
WBStrain00004981
WBStrain00005008
WBStrain00005829
WBStrain00006190
WBStrain00006361
WBStrain00007936
WBStrain00008056
WBStrain00005019
WBStrain00005025
WBStrain00047343
WBStrain00047344
WBStrain00047339
WBStrain00047342
WBStrain00051010
WBStrain00051965
RNASeq_FPKM (74)
GO_annotation (27)
Ortholog (46)
Structured_descriptionAutomated_descriptionEnables RNA polymerase II transcription regulatory region sequence-specific DNA binding activity; histone acetyltransferase binding activity; and identical protein binding activity. Involved in several processes, including dauer larval development; neuron differentiation; and positive regulation of transcription by RNA polymerase II. Located in nucleus. Expressed in ABalappaap; ABalappaapp; and neurons. Human ortholog(s) of this gene implicated in hypotonia, ataxia, and delayed development syndrome. Is an ortholog of several human genes including EBF1 (EBF transcription factor 1); EBF2 (EBF transcription factor 2); and EBF4 (EBF family member 4).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:0081176Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:19087)
Molecular_infoCorresponding_CDSY16B4A.1
Corresponding_CDS_historyY16B4A.1:wp62
Corresponding_transcriptY16B4A.1.1
Other_sequence (23)
Associated_featureWBsf648757
WBsf648758
WBsf663592
WBsf663593
WBsf663594
WBsf663595
WBsf663596
WBsf978939
WBsf1008002
WBsf1008003
WBsf1008004
WBsf1008005
WBsf1008006
WBsf1008007
WBsf1024459
WBsf1024460
WBsf1024461
WBsf1024462
WBsf236718
Transcription_factorWBTranscriptionFactor000217
Experimental_infoRNAi_resultWBRNAi00115872Inferred_automaticallyRNAi_primary
WBRNAi00090173Inferred_automaticallyRNAi_primary
WBRNAi00090014Inferred_automaticallyRNAi_primary
WBRNAi00027739Inferred_automaticallyRNAi_primary
WBRNAi00020068Inferred_automaticallyRNAi_primary
WBRNAi00055554Inferred_automaticallyRNAi_primary
WBRNAi00062789Inferred_automaticallyRNAi_primary
WBRNAi00008787Inferred_automaticallyRNAi_primary
WBRNAi00090332Inferred_automaticallyRNAi_primary
WBRNAi00089778Inferred_automaticallyRNAi_primary
Expr_pattern (13)
Drives_construct (11)
Construct_product (14)
AntibodyWBAntibody00000177
Microarray_results (21)
Expression_cluster (188)
Interaction (195)
Map_infoMapXPosition21.3208Error0.014822
Well_ordered
PositivePositive_cloneF42D1
Y16B4AInferred_automaticallyFrom sequence, transcript, pseudogene data
NegativeNegative_cloneK01B4
Mapping_data2_point (52)
Multi_point (53)
Pos_neg_data (39)
Landmark_gene
Reference (217)
Remark[Eddy SR] EcoRV RFLP correlated with unc-3. 3.8 kb EcoRV band in N2, 2.3 kb in unc-3 (mn419), 3.8 kb again in revertants unc-3 (mn419 mn422) and unc-3 (mn419 mn426), 3.7 kb in revertant unc-3 (mn419 mn431).
Polymorphism detection method = Southern hybridisation krb 04/03/02
MethodGene