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WormBase Tree Display for Gene: WBGene00000487

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Name Class

WBGene00000487SMapS_parentSequenceC23H5
IdentityVersion2
NameCGC_nameche-6Person_evidenceWBPerson261
WBPerson260
Sequence_nameC23H5.7
Molecular_nameC23H5.7
C23H5.7.1
CE52177
Other_namecng-4Person_evidenceWBPerson260
CELE_C23H5.7Accession_evidenceNDBBX284604
Public_nameche-6
DB_infoDatabaseWormFluxgeneWBGene00000487
NDBlocus_tagCELE_C23H5.7
PanthergeneCAEEL|WormBase=WBGene00000487|UniProtKB=O61827
familyPTHR45638
NCBIgene182823
RefSeqproteinNM_001356910.3
TREEFAMTREEFAM_IDTF319048
TrEMBLUniProtAccO61827
UniProt_GCRPUniProtAccO61827
OMIMgene123825
600053
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:21WBPerson1971EventImportedInitial conversion from geneace
215 Aug 2012 10:29:53WBPerson2970EventAcquires_mergeWBGene00016026
Name_changeSequence_nameC23H5.7
Other_namecng-4
Acquires_mergeWBGene00016026
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classche
Reference_alleleWBVar00143765
Allele (165)
Legacy_informatione1126 : non-chemotactic to chloride ion; abnormal IL2 basal bodies. ES1 ME3. NA1.
See also e1126
[C.elegansII] e1126 : non-chemotactic to chloride ion; abnormal IL2 basal bodies. ES1 ME3. NA1. [Lewis and Hodgkin 1977]
StrainWBStrain00022728
WBStrain00022733
WBStrain00004250
RNASeq_FPKM (74)
GO_annotation (16)
Ortholog (36)
ParalogWBGene00006526Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00006525Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00000562Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00000563Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00022295Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00001171Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00006830Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable cGMP binding activity; intracellular cAMP-activated cation channel activity; and intracellular cGMP-activated cation channel activity. Predicted to be involved in monoatomic cation transmembrane transport. Located in neuronal cell body. Expressed in ASEL; ASER; AWCL; and AWCR. Human ortholog(s) of this gene implicated in achromatopsia 2 and retinitis pigmentosa 49. Is an ortholog of several human genes including CNGA1 (cyclic nucleotide gated channel subunit alpha 1); CNGA2 (cyclic nucleotide gated channel subunit alpha 2); and CNGA3 (cyclic nucleotide gated channel subunit alpha 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_infoPotential_modelDOID:13399Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2150)
DOID:0110377Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2148)
DOID:0110007Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2150)
DOID:10584Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2148)
Molecular_infoCorresponding_CDSC23H5.7
Corresponding_CDS_historyC23H5.7:wp239
C23H5.7:wp261
Corresponding_transcriptC23H5.7.1
Other_sequenceFG354142.1
JI168297.1
Associated_featureWBsf995623
WBsf1016860
Experimental_infoRNAi_resultWBRNAi00076157Inferred_automaticallyRNAi_primary
WBRNAi00041037Inferred_automaticallyRNAi_primary
WBRNAi00011068Inferred_automaticallyRNAi_primary
Expr_patternExpr11202
Expr1145077
Expr2009967
Expr2028207
Drives_constructWBCnstr00018218
Microarray_results (18)
Expression_cluster (53)
Map_infoMapIVPosition-11.0452
PositivePositive_cloneC23H5Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (15)
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