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WormBase Tree Display for Gene: WBGene00009929

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Name Class

WBGene00009929SMapS_parentSequenceF52D10
IdentityVersion2
NameCGC_nameabts-2Person_evidenceWBPerson2233
Sequence_nameF52D10.1
Molecular_nameF52D10.1
F52D10.1.1
CE40613
Other_nameCELE_F52D10.1Accession_evidenceNDBBX284606
Public_nameabts-2
DB_infoDatabaseAceViewgeneXM209
WormQTLgeneWBGene00009929
WormFluxgeneWBGene00009929
NDBlocus_tagCELE_F52D10.1
PanthergeneCAEEL|WormBase=WBGene00009929|UniProtKB=G5EGB9
familyPTHR11453
NCBIgene186108
RefSeqproteinNM_077535.8
TrEMBLUniProtAccG5EGB9
UniProt_GCRPUniProtAccG5EGB9
OMIMgene610206
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:50WBPerson1971EventImportedInitial conversion from CDS class of WS125
219 Jan 2005 16:30:54WBPerson2970Name_changeCGC_nameabts-2
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classabts
Allele (58)
RNASeq_FPKM (74)
GO_annotation (15)
Ortholog (38)
ParalogWBGene00009920Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00019018Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00019844Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
Structured_descriptionConcise_descriptionabts-2 encodes an anion transporter; when expressed in Xenopus oocytes, ABTS-2 does not exhibit detectable transport of chloride, sulfate, or oxolate anions; ABTS-2::GFP fusion proteins are expressed in the larval excretory cell and the adult ovaries, while an abts-2::gfp promoter fusion is seen in only one tail ganglion neuron; in intestinal cells, the ABTS-2::GFP fusion protein localizes to the basolateral membrane.Paper_evidenceWBPaper00025075
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated13 Dec 2007 00:00:00
Automated_descriptionPredicted to enable transmembrane transporter activity. Predicted to be involved in monoatomic ion homeostasis and transmembrane transport. Located in basolateral plasma membrane. Expressed in dorsal-rectal ganglion neurons; gonadal sheath cell; and tail neurons. Human ortholog(s) of this gene implicated in Fuchs' endothelial dystrophy; congenital hereditary endothelial dystrophy of cornea; and corneal dystrophy-perceptive deafness syndrome. Is an ortholog of human SLC4A11 (solute carrier family 4 member 11).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:0060649Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:16438)
DOID:11555Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:16438)
DOID:0111620Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:16438)
Molecular_infoCorresponding_CDSF52D10.1
Corresponding_CDS_historyF52D10.1:wp54
F52D10.1:wp109
F52D10.1:wp155
Corresponding_transcriptF52D10.1.1
Other_sequenceSSC04413_1
SS02624
Associated_featureWBsf1007049
WBsf236404
WBsf236405
Experimental_infoRNAi_resultWBRNAi00066583Inferred_automaticallyRNAi_primary
WBRNAi00015394Inferred_automaticallyRNAi_primary
WBRNAi00047961Inferred_automaticallyRNAi_primary
WBRNAi00032604Inferred_automaticallyRNAi_primary
Expr_patternChronogram452
Expr3243
Expr3254
Expr6137
Expr1025501
Expr1151780
Expr2009100
Expr2027336
Drives_constructWBCnstr00003945
WBCnstr00011246
WBCnstr00011257
WBCnstr00031807
Construct_productWBCnstr00011257
WBCnstr00031807
Microarray_results (18)
Expression_cluster (102)
InteractionWBInteraction000032150
WBInteraction000142939
WBInteraction000296106
WBInteraction000407567
WBInteraction000543495
Map_infoMapXPosition4.79868Error0.039026
PositivePositive_cloneF52D10Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point5040
5432
Pseudo_map_position
ReferenceWBPaper00025075
WBPaper00038491
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