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WormBase Tree Display for Gene: WBGene00016613

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Name Class

WBGene00016613SMapS_parentSequenceC43G2
IdentityVersion2
NameCGC_namebest-9Person_evidenceWBPerson260
Sequence_nameC43G2.4
Molecular_nameC43G2.4
C43G2.4.1
CE34750
C43G2.4.2
C43G2.4.3
Other_nameCELE_C43G2.4Accession_evidenceNDBBX284604
Public_namebest-9
DB_infoDatabaseAceViewgene4H329
WormQTLgeneWBGene00016613
WormFluxgeneWBGene00016613
NDBlocus_tagCELE_C43G2.4
PanthergeneCAEEL|WormBase=WBGene00016613|UniProtKB=Q94175
familyPTHR10736
NCBIgene183419
RefSeqproteinNM_001392319.1
SwissProtUniProtAccQ94175
UniProt_GCRPUniProtAccQ94175
OMIMgene607854
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:57WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
207 Feb 2012 16:30:56WBPerson2970Name_changeCGC_namebest-9
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classbest
Allele (63)
RNASeq_FPKM (74)
GO_annotation00087264
00087265
00087266
00087267
00087268
00087269
00087270
00087271
00087272
00122196
Ortholog (35)
Paralog (26)
Structured_descriptionAutomated_descriptionPredicted to enable chloride channel activity. Predicted to be involved in chloride transmembrane transport. Predicted to be located in plasma membrane. Predicted to be part of chloride channel complex. Human ortholog(s) of this gene implicated in autosomal dominant vitreoretinochoroidopathy and retinal degeneration (multiple). Is an ortholog of human BEST1 (bestrophin 1) and BEST3 (bestrophin 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:0110396Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12703)
DOID:4448Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12703)
DOID:0050661Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12703)
DOID:0050662Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12703)
DOID:0111569Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12703)
Molecular_infoCorresponding_CDSC43G2.4
Corresponding_CDS_historyC43G2.4:wp104
Corresponding_transcriptC43G2.4.1
C43G2.4.2
C43G2.4.3
Other_sequence (12)
Associated_featureWBsf646021
WBsf660234
WBsf660235
WBsf996768
WBsf1017539
WBsf228426
WBsf228427
Experimental_infoRNAi_resultWBRNAi00029771Inferred_automaticallyRNAi_primary
WBRNAi00042397Inferred_automaticallyRNAi_primary
Expr_patternExpr1028232
Expr1037136
Expr1146389
Expr2009614
Expr2027852
Drives_constructWBCnstr00027937
Construct_productWBCnstr00027937
Microarray_results (26)
Expression_cluster (99)
InteractionWBInteraction000275271
WBInteraction000322439
WBInteraction000439552
Map_infoMapIVPosition3.20546
PositivePositive_cloneC43G2Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00055090
WBPaper00064809
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