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WormBase Tree Display for Gene: WBGene00004058

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Name Class

WBGene00004058EvidencePerson_evidenceWBPerson583
WBPerson36
SMapS_parentSequenceC44B7
IdentityVersion1
NameCGC_namepmp-1Person_evidenceWBPerson36
Sequence_nameC44B7.8
Molecular_nameC44B7.8
C44B7.8.1
CE02546
Other_nameCELE_C44B7.8Accession_evidenceNDBBX284602
Public_namepmp-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:34WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classpmp
Allele (35)
StrainWBStrain00031620
RNASeq_FPKM (74)
GO_annotation (24)
Ortholog (36)
ParalogWBGene00004059Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00004061Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00004060Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00004062Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionpmp-1 encodes an ATP-binding cassette (ABC) transporter most closely related to the peroxisomal membrane proteins; pmp-1 activity is required for efficient RNA interference (RNAi) of a germline-expressed target, pop-1.Paper_evidenceWBPaper00027644
Curator_confirmedWBPerson1843
Date_last_updated09 Mar 2007 00:00:00
Automated_descriptionPredicted to enable ATP binding activity; ATPase-coupled transmembrane transporter activity; and long-chain fatty acid transporter activity. Predicted to be involved in fatty acid catabolic process; long-chain fatty acid import into peroxisome; and peroxisome organization. Predicted to be located in peroxisomal membrane. Human ortholog(s) of this gene implicated in Zellweger syndrome and congenital bile acid synthesis defect 5. Is an ortholog of human ABCD3 (ATP binding cassette subfamily D member 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:905Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:67)
DOID:0111066Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:67)
Molecular_infoCorresponding_CDSC44B7.8
Corresponding_transcriptC44B7.8.1
Other_sequenceGW412065.1
PSC01354_1
FF678460.1
HG08107
FF680123.1
BXC02039_1
JI477427.1
Associated_featureWBsf650193
WBsf223246
Experimental_infoRNAi_resultWBRNAi00102606Inferred_automaticallyRNAi_primary
WBRNAi00042433Inferred_automaticallyRNAi_primary
WBRNAi00103674Inferred_automaticallyRNAi_primary
WBRNAi00029788Inferred_automaticallyRNAi_primary
Expr_patternExpr5495
Expr1027941
Expr1031956
Expr1146422
Expr2014972
Expr2033207
Drives_constructWBCnstr00002194
WBCnstr00035718
Construct_productWBCnstr00035718
Microarray_results (22)
Expression_cluster (229)
Interaction (38)
Map_infoMapIIPosition0.13231Error0.001303
PositivePositive_cloneC44B7Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00026800
WBPaper00026805
WBPaper00027644
WBPaper00031484
WBPaper00038491
WBPaper00047097
WBPaper00055090
WBPaper00061133
WBPaper00061938
WBPaper00065331
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