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WormBase Tree Display for Gene: WBGene00000169

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Name Class

WBGene00000169EvidencePerson_evidenceWBPerson548
SMapS_parentSequenceF32A5
IdentityVersion2
NameCGC_nameaqp-1Person_evidenceWBPerson300
Sequence_nameF32A5.5
Molecular_nameF32A5.5a
F32A5.5a.1
CE29304
F32A5.5b
CE01275
F32A5.5b.1
Other_namedod-4
CELE_F32A5.5Accession_evidenceNDBBX284602
Public_nameaqp-1
DB_infoDatabaseAceViewgene2H526
WormQTLgeneWBGene00000169
WormFluxgeneWBGene00000169
NDBlocus_tagCELE_F32A5.5
PanthergeneCAEEL|WormBase=WBGene00000169|UniProtKB=Q19949
familyPTHR43829
NCBIgene174190
RefSeqproteinNM_063109.6
NM_001381493.2
TREEFAMTREEFAM_IDTF313173
TrEMBLUniProtAccQ19949
Q8IG23
UniProt_GCRPUniProtAccQ19949
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:20WBPerson1971EventImportedInitial conversion from geneace
225 Aug 2004 11:36:28WBPerson1971Name_changeOther_namedod-4
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classaqp
AlleleWBVar00742918
WBVar00742919
WBVar00742920
WBVar01499702
WBVar00742921
WBVar00742922
WBVar00742923
WBVar00742924
WBVar00742925
WBVar00742926
WBVar00742927
WBVar00742928
WBVar00369790
WBVar00742929
WBVar00369791
WBVar00742930
WBVar00369792
WBVar00742931
WBVar00369793
WBVar00742932
WBVar00225615
WBVar00742933
WBVar00742934
WBVar00173204
WBVar00742935
WBVar01498435
WBVar02130211
WBVar00251211
WBVar00598432
WBVar00104486
WBVar00104487
WBVar01498940
WBVar00742916
WBVar00742917
StrainWBStrain00004916
RNASeq_FPKM (74)
GO_annotation (23)
Ortholog (40)
ParalogWBGene00000171Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00000176Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00000175Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00013272Caenorhabditis elegansFrom_analysisPanther
WBGene00000170Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00000172Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00000173Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00000174Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionaqp-1 encodes, by alternative splicing, two isoforms of an aquaglyceroporin required for normally short lifespan; AQP-1 expression is upregulated under daf-2(-) conditions, and loss of AQP-1 function in daf-2 mutant animals results in reduced lifespan; AQP-1 increases glycerol permeability five- to seven-fold when expressed in Xenopus oocytes; AQP-1::GFP fusion proteins are expressed predominantly in the intestine, where they localize to the basolateral plasma membrane, but are also expressed in the pharynx; intestinal expression of AQP-1 is repressed by infection with Pseudomonas aeruginosa.Paper_evidenceWBPaper00005976
WBPaper00028482
WBPaper00029039
WBPaper00030907
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated12 Aug 2007 00:00:00
Automated_descriptionEnables channel activity. Involved in defense response to Gram-negative bacterium; glycerol transmembrane transport; and innate immune response. Located in basolateral plasma membrane. Expressed in intestine and pharynx. Human ortholog(s) of this gene implicated in several diseases, including brain edema; inflammatory bowel disease (multiple); and morbid obesity. Is an ortholog of several human genes including AQP3 (aquaporin 3 (Gill blood group)); AQP7 (aquaporin 7); and AQP9 (aquaporin 9).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:4724Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:636)
DOID:8577Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:640)
DOID:8778Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:640)
DOID:9352Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:640)
DOID:0060180Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:640)
DOID:11981Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:640)
Molecular_infoCorresponding_CDSF32A5.5a
F32A5.5b
Corresponding_transcriptF32A5.5a.1
F32A5.5b.1
Other_sequence (15)
Associated_featureWBsf019168
WBsf650216
WBsf650217
WBsf223316
Experimental_infoRNAi_resultWBRNAi00097044Inferred_automaticallyRNAi_primary
WBRNAi00094564Inferred_automaticallyRNAi_primary
WBRNAi00014195Inferred_automaticallyRNAi_primary
WBRNAi00063161Inferred_automaticallyRNAi_primary
WBRNAi00031645Inferred_automaticallyRNAi_primary
WBRNAi00046077Inferred_automaticallyRNAi_primary
WBRNAi00097048Inferred_automaticallyRNAi_primary
WBRNAi00094561Inferred_automaticallyRNAi_primary
Expr_patternExpr4771
Expr1017935
Expr1149967
Expr2009379
Expr2027615
Drives_constructWBCnstr00012231
WBCnstr00017137
WBCnstr00037691
Construct_productWBCnstr00012231
WBCnstr00017137
WBCnstr00037691
Microarray_results (25)
Expression_cluster (279)
Interaction (92)
Map_infoMapIIPosition0.499703Error3.1e-05
PositivePositive_cloneF32A5Inferred_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