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WormBase Tree Display for Gene: WBGene00022797

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Name Class

WBGene00022797SMapS_parentSequenceZK688
IdentityVersion2
NameCGC_namebest-24Person_evidenceWBPerson260
Sequence_nameZK688.2
Molecular_nameZK688.2
ZK688.2.1
CE00460
Other_nameCELE_ZK688.2Accession_evidenceNDBBX284603
Public_namebest-24
DB_infoDatabaseAceViewgene3I993
WormQTLgeneWBGene00022797
WormFluxgeneWBGene00022797
NDBlocus_tagCELE_ZK688.2
PanthergeneCAEEL|WormBase=WBGene00022797|UniProtKB=P34672
familyPTHR10736
NCBIgene176110
RefSeqproteinNM_066316.8
SwissProtUniProtAccP34672
UniProt_GCRPUniProtAccP34672
OMIMgene607854
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:06WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
207 Feb 2012 16:30:56WBPerson2970Name_changeCGC_namebest-24
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classbest
Allele (38)
StrainWBStrain00003420
WBStrain00051454
RNASeq_FPKM (74)
GO_annotation (12)
Ortholog (46)
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. Expressed in head neurons; hypodermis; intestine; and nervous system. Human ortholog(s) of this gene implicated in autosomal dominant vitreoretinochoroidopathy and retinal degeneration (multiple). Is an ortholog of human BEST2 (bestrophin 2) and BEST4 (bestrophin 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: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_CDSZK688.2
Corresponding_transcriptZK688.2.1
Other_sequence (28)
Associated_featureWBsf993187
WBsf225297
WBsf225298
Experimental_infoRNAi_resultWBRNAi00070770Inferred_automaticallyRNAi_primary
WBRNAi00066737Inferred_automaticallyRNAi_primary
WBRNAi00066550Inferred_automaticallyRNAi_primary
WBRNAi00005215Inferred_automaticallyRNAi_primary
WBRNAi00038421Inferred_automaticallyRNAi_primary
WBRNAi00059670Inferred_automaticallyRNAi_primary
WBRNAi00070771Inferred_automaticallyRNAi_primary
WBRNAi00022133Inferred_automaticallyRNAi_primary
Expr_patternChronogram344
Expr7243
Expr1018157
Expr1040085
Expr1163085
Expr2009606
Expr2027843
Drives_constructWBCnstr00003887
WBCnstr00023966
Construct_productWBCnstr00023966
Microarray_results (19)
Expression_cluster (184)
Interaction (29)
Map_infoMapIIIPosition-0.5041
PositivePositive_cloneZK688Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00055090
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