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WormBase Tree Display for Gene: WBGene00007703

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Name Class

WBGene00007703SMapS_parentSequenceCHROMOSOME_III
IdentityVersion3
NameCGC_namegbf-1Person_evidenceWBPerson508
Sequence_nameC24H11.7
Molecular_nameC24H11.7a
C24H11.7a.1
CE44078
C24H11.7b
CE47290
C24H11.7b.1
Other_namephi-34Person_evidenceWBPerson2582
CELE_C24H11.7Accession_evidenceNDBBX284603
Public_namegbf-1
DB_infoDatabaseAceViewgene3M842
WormQTLgeneWBGene00007703
WormFluxgeneWBGene00007703
NDBlocus_tagCELE_C24H11.7
PanthergeneCAEEL|WormBase=WBGene00007703|UniProtKB=G5EGS5
familyPTHR10663
NCBIgene176609
RefSeqproteinNM_001379939.1
NM_001379938.2
SwissProtUniProtAccG5EGS5
UniProt_GCRPUniProtAccG5EGS5
OMIMgene603698
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:48WBPerson1971EventImportedInitial conversion from CDS class of WS125
218 Feb 2005 12:07:44WBPerson2970Name_changeCGC_namegbf-1
317 Mar 2005 13:54:35WBPerson2970Name_changeOther_namephi-34
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classgbf
Allele (623)
RNASeq_FPKM (74)
GO_annotation (17)
Ortholog (48)
ParalogWBGene00001743Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00008685Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00012386Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00013223Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00019726Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable guanyl-nucleotide exchange factor activity. Involved in endosomal transport; organelle organization; and secretion. Located in Golgi cis cisterna and endoplasmic reticulum exit site. Human ortholog(s) of this gene implicated in Charcot-Marie-Tooth disease dominant intermediate A. Is an ortholog of human GBF1 (golgi brefeldin A resistant guanine nucleotide exchange factor 1).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:0110202Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4181)
Molecular_infoCorresponding_CDSC24H11.7a
C24H11.7b
Corresponding_CDS_historyC24H11.7:wp183
C24H11.7:wp206
Corresponding_transcriptC24H11.7a.1
C24H11.7b.1
Other_sequence (53)
Associated_featureWBsf667453
WBsf667454
WBsf667455
WBsf994483
WBsf994484
WBsf994485
WBsf994486
WBsf1016076
WBsf227598
Experimental_infoRNAi_result (22)
Expr_patternExpr1029033
Expr1033332
Expr1145155
Expr2011957
Expr2030194
AntibodyWBAntibody00002462
Microarray_results (19)
Expression_cluster (79)
Interaction (74)
Map_infoMapIIIPosition12.2356Error0.075847
PositivePositive_cloneC24H11Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00036769
WBPaper00038491
WBPaper00042578
WBPaper00045696
WBPaper00047001
WBPaper00050112
WBPaper00055090
WBPaper00064389
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