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WormBase Tree Display for Gene: WBGene00004059

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Name Class

WBGene00004059EvidencePerson_evidenceWBPerson583
WBPerson36
SMapS_parentSequenceC44B7
IdentityVersion1
NameCGC_namepmp-2Person_evidenceWBPerson36
Sequence_nameC44B7.9
Molecular_nameC44B7.9
C44B7.9.1
CE02547
Other_nameCELE_C44B7.9Accession_evidenceNDBBX284602
Public_namepmp-2
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:34WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classpmp
Allele (50)
StrainWBStrain00001191
WBStrain00001814
WBStrain00037764
RNASeq_FPKM (74)
GO_annotation00061771
00061772
00061773
00061774
00061775
00061776
00061777
00061778
00061779
00061780
00061781
00061782
00061783
00061784
00061785
00112312
00112313
00112314
00112315
00112316
00112317
00112318
00112319
00112320
Ortholog (36)
ParalogWBGene00004058Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00004060Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00004061Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00004062Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionAutomated_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. Expressed in intestine. 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_CDSC44B7.9
Corresponding_transcriptC44B7.9.1
Other_sequence (51)
Associated_featureWBsf650194
WBsf981214
WBsf223247
Experimental_infoRNAi_resultWBRNAi00103675Inferred_automaticallyRNAi_primary
WBRNAi00029789Inferred_automaticallyRNAi_primary
WBRNAi00042434Inferred_automaticallyRNAi_primary
WBRNAi00102607Inferred_automaticallyRNAi_primary
WBRNAi00102855Inferred_automaticallyRNAi_primary
WBRNAi00011916Inferred_automaticallyRNAi_primary
Expr_patternExpr5496
Expr1019896
Expr1031957
Expr1146423
Expr2014973
Expr2033208
Drives_constructWBCnstr00002084
WBCnstr00035717
Construct_productWBCnstr00035717
Microarray_results (20)
Expression_cluster (153)
Interaction (37)
Map_infoMapIIPosition0.13554Error0.001335
PositivePositive_cloneC44B7Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (6)
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