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WormBase Tree Display for Gene: WBGene00006809

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Name Class

WBGene00006809SMapS_parentSequenceC11D2
IdentityVersion2
NameCGC_nameunc-77Person_evidenceWBPerson261
Sequence_nameC11D2.6
Molecular_name (48)
Other_namenca-1Paper_evidenceWBPaper00031592
Person_evidenceWBPerson604
CELE_C11D2.6Accession_evidenceNDBBX284604
Public_nameunc-77
DB_infoDatabaseWormQTLgeneWBGene00006809
WormFluxgeneWBGene00006809
NDBlocus_tagCELE_C11D2.6
PanthergeneCAEEL|WormBase=WBGene00006809|UniProtKB=V6CKM5
familyPTHR46141
NCBIgene177379
RefSeqprotein (16)
TREEFAMTREEFAM_IDTF312843
TrEMBLUniProtAcc (16)
UniProt_GCRPUniProtAccV6CKM5
OMIMgene611549
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:43WBPerson1971EventImportedInitial conversion from geneace
203 Dec 2009 11:55:50WBPerson2970EventAcquires_mergeWBGene00003557
Acquires_mergeWBGene00003557
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classunc
Reference_alleleWBVar00143348
Allele (298)
Legacy_informatione625 : irregular loopy movement both forward and reverse; active; thin; sometimes protrusive vulva. Slight movement abnormality in e625/+. ES2 ME2 NA1.
[C.elegansII] e625 : irregular loopy movement both forward and reverse; active; thin; sometimes protrusive vulva. Slight movement abnormality in e625/+. ES2 ME2 NA1. [Brenner 1974]
StrainWBStrain00035028
WBStrain00035029
WBStrain00035482
WBStrain00040855
WBStrain00040862
WBStrain00040863
WBStrain00040864
WBStrain00040865
WBStrain00006352
Component_of_genotypeWBGenotype00000089
WBGenotype00000090
WBGenotype00000091
RNASeq_FPKM (74)
GO_annotation (18)
Ortholog (51)
ParalogWBGene00003558Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00000367Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001187Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00006742Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00008911Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionunc-77 encodes, along with nca-2, one of two C. elegans alpha-1-like subunits of a voltage-insensitive cation leak channel related to Drosophila narrow abdomen and the vertebrate Vgcnl1/NALCN proteins; unc-77 functions redundantly with nca-2 to transmit depolarization signals from neuronal cell bodies to axons, thus regulating presynaptic activation; unc-77 and nca-2 are also required for normal locomotion and the response to specific volatile anesthetics; in regulating synaptic activity, unc-77 appears to function in the same pathway as unc-79 and unc-80, which encode novel conserved proteins that reciprocally regulate UNC-77 expression; co-expression of UNC-77 and UNC-80 in HEK293T cells results in increased UNC-77 channel activity, in a manner consistent with UNC-77 and UNC-80 functioning as an ion leak channel; an unc-77::gfp reporter fusion is expressed in many sensory and all motoneurons; in the dorsal and ventral nerve cords, UNC-77 localizes to specific axonal regions, but not to synapses.Paper_evidenceWBPaper00030757
WBPaper00031000
WBPaper00031592
Curator_confirmedWBPerson1843
Date_last_updated22 Jun 2010 00:00:00
Automated_descriptionEnables monoatomic cation channel activity. Involved in positive regulation of GABAergic synaptic transmission; positive regulation of cholinergic synaptic transmission; and positive regulation of locomotion. Located in axon. Expressed in cholinergic neurons; nerve ring; pharyngeal neurons; and tail ganglion. Used to study congenital limbs-face contractures-hypotonia-developmental delay syndrome. Human ortholog(s) of this gene implicated in congenital limbs-face contractures-hypotonia-developmental delay syndrome. Is an ortholog of human NALCN (sodium leak channel, non-selective).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:0081048Homo sapiensPaper_evidenceWBPaper00046648
Curator_confirmedWBPerson324
Date_last_updated09 Feb 2022 00:00:00
Potential_modelEFO:MONDO:0014176Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:19082)
DOID:0081048Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:19082)
Models_disease_assertedWBDOannot00001101
WBDOannot00001105
Molecular_infoCorresponding_CDS (16)
Corresponding_CDS_historyC11D2.6a:wp239
C11D2.6b:wp239
C11D2.6c:wp239
Corresponding_transcript (16)
Other_sequence (15)
Associated_featureWBsf651837
WBsf996705
WBsf996706
WBsf996707
WBsf996708
WBsf996709
WBsf1017492
WBsf1017493
WBsf230141
WBsf230142
Experimental_infoRNAi_result (15)
Expr_patternChronogram197
Expr4860
Expr5240
Expr8058
Expr8060
Expr8194
Expr8324
Expr1144413
Expr2017906
Expr2036042
Drives_construct (12)
Construct_productWBCnstr00017151
WBCnstr00021676
WBCnstr00021677
WBCnstr00021678
WBCnstr00021679
WBCnstr00021680
WBCnstr00021681
WBCnstr00037886
AntibodyWBAntibody00001260
WBAntibody00001384
Microarray_results (48)
Expression_cluster (190)
Interaction (21)
Map_infoMapIVPosition3.08555
PositivePositive_cloneC11D2Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_data2_point323
Multi_point1422
4509
ReferenceWBPaper00000031
WBPaper00000608
WBPaper00002487
WBPaper00005617
WBPaper00010206
WBPaper00010687
WBPaper00016710
WBPaper00017184
WBPaper00017588
WBPaper00019702
WBPaper00024163
WBPaper00024867
WBPaper00025141
WBPaper00025465
WBPaper00026083
WBPaper00026474
WBPaper00027304
WBPaper00027751
WBPaper00028212
WBPaper00029029
WBPaper00030406
WBPaper00030757
WBPaper00031000
WBPaper00031592
WBPaper00031982
WBPaper00033356
WBPaper00035956
WBPaper00038491
WBPaper00038849
WBPaper00040141
WBPaper00042167
WBPaper00043908
WBPaper00046648
WBPaper00048388
WBPaper00050947
WBPaper00051462
WBPaper00053144
WBPaper00053150
WBPaper00053216
WBPaper00055090
WBPaper00063950
WBPaper00066271
MethodGene