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WormBase Tree Display for Gene: WBGene00004191

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Name Class

WBGene00004191SMapS_parentSequenceC11H1
IdentityVersion1
NameCGC_nameprx-1
Sequence_nameC11H1.4
Molecular_nameC11H1.4a
C11H1.4a.1
CE30339
C11H1.4b
CE05265
C11H1.4b.1
Other_namepex-1Paper_evidenceWBPaper00004835
WBPaper00018161
WBPaper00005418
WBPaper00005877
pex1Accession_evidenceEMBLAB054992
C11H1.6Paper_evidenceWBPaper00005418
CELE_C11H1.4Accession_evidenceNDBBX284606
Public_nameprx-1
DB_infoDatabaseWormQTLgeneWBGene00004191
WormFluxgeneWBGene00004191
NDBlocus_tagCELE_C11H1.4
PanthergeneCAEEL|WormBase=WBGene00004191|UniProtKB=G5ED99
familyPTHR23077
NCBIgene181538
RefSeqproteinNM_001381145.1
NM_077985.7
TREEFAMTREEFAM_IDTF106447
TrEMBLUniProtAccG5ED99
A6ZJ67
UniProt_GCRPUniProtAccG5ED99
OMIMgene602136
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:34WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classprx
Allele (302)
StrainWBStrain00035803
RNASeq_FPKM (74)
GO_annotation00005027
00005028
00005029
00005030
00005031
00005032
00112456
00112457
00112458
00112459
Ortholog (35)
ParalogWBGene00003119Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00007352Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00008053Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00004195Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00010562Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00013156Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionprx-1 encodes a predicted peroxin, a subfamily 2 member of the AAA (ATPases Associated with diverse cellular Activities) family that affects growth in one large-scale RNAi screen; expressed in intestinal cells throughout development.Paper_evidenceWBPaper00004835
WBPaper00006395
Curator_confirmedWBPerson48
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable ATP hydrolysis activity. Predicted to be involved in protein import into peroxisome matrix. Predicted to be located in cytosol and peroxisomal membrane. Human ortholog(s) of this gene implicated in Heimler syndrome 1; peroxisome biogenesis disorder 1A; and peroxisome biogenesis disorder 1B. Is an ortholog of human PEX1 (peroxisomal biogenesis 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:0080623Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8850)
DOID:0080476Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8850)
DOID:0081240Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8850)
Molecular_infoCorresponding_CDSC11H1.4a
C11H1.4b
Corresponding_CDS_historyC11H1.4:wp74
Corresponding_transcriptC11H1.4a.1
C11H1.4b.1
Other_sequence (19)
Associated_feature (18)
Experimental_infoRNAi_resultWBRNAi00028813Inferred_automaticallyRNAi_primary
WBRNAi00062860Inferred_automaticallyRNAi_primary
WBRNAi00040366Inferred_automaticallyRNAi_primary
WBRNAi00024539Inferred_automaticallyRNAi_primary
WBRNAi00040365Inferred_automaticallyRNAi_primary
WBRNAi00024538Inferred_automaticallyRNAi_primary
WBRNAi00010633Inferred_automaticallyRNAi_primary
WBRNAi00027170Inferred_automaticallyRNAi_primary
WBRNAi00010631Inferred_automaticallyRNAi_primary
WBRNAi00007234Inferred_automaticallyRNAi_primary
Expr_patternExpr1637
Expr1022255
Expr1032051
Expr1144429
Expr2015124
Expr2033362
Microarray_results (25)
Expression_cluster (82)
Interaction (72)
Map_infoMapXPosition16.6804Error0.001645
PositivePositive_cloneC11H1Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4254
4606
5538
Pseudo_map_position
Reference (12)
RemarkSequence connection from [Motley AM, Plasterk RHA], 02/06/13 krb.
The connected sequence (C11H1.4) was previously C11H1.6 (the C11H1.4 gene was extended and incorporated C11H1.6). krb
Map 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