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WormBase Tree Display for Gene: WBGene00018013

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Name Class

WBGene00018013SMapS_parentSequenceF33E11
IdentityVersion3
NameCGC_namephf-10Person_evidenceWBPerson260
Sequence_nameF33E11.6
Molecular_nameF33E11.6a
F33E11.6a.1
CE39928
F33E11.6b
CE39929
F33E11.6c
CE28295
F33E11.6b.1
F33E11.6c.1
Other_nameCELE_F33E11.6Accession_evidenceNDBBX284605
Public_namephf-10
DB_infoDatabaseAceViewgene5A784
WormQTLgeneWBGene00018013
WormFluxgeneWBGene00018013
NDBlocus_tagCELE_F33E11.6
PanthergeneCAEEL|WormBase=WBGene00018013|UniProtKB=Q2A950
familyPTHR10615
NCBIgene3565141
RefSeqproteinNM_001047647.6
NM_001047648.4
NM_001313168.3
TREEFAMTREEFAM_IDTF318971
TrEMBLUniProtAccA0A0K3AS00
Q2A950
Q2A949
UniProt_GCRPUniProtAccQ2A950
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:59WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
202 Mar 2006 09:46:46WBPerson1867EventAcquires_mergeWBGene00018012
314 Oct 2011 15:24:19WBPerson2970Name_changeCGC_namephf-10
Acquires_mergeWBGene00018012
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classphf
Allele (133)
RNASeq_FPKM (74)
GO_annotation00000891
00000892
00000893
00080250
Contained_in_operonCEOP5012
Ortholog (32)
ParalogWBGene00007029Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00007914Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00016200Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00045419Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00010537Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable metal ion binding activity. Predicted to be involved in nervous system development. Predicted to be located in nucleus. Used to study alcohol use disorder. Is an ortholog of human PHF10 (PHD finger protein 10).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_infoExperimental_modelDOID:1574Homo sapiensPaper_evidenceWBPaper00046494
Curator_confirmedWBPerson324
Date_last_updated20 May 2019 00:00:00
Models_disease_in_annotationWBDOannot00000671
Molecular_infoCorresponding_CDSF33E11.6a
F33E11.6b
F33E11.6c
Corresponding_CDS_historyF33E11.6:wp155
Corresponding_transcriptF33E11.6a.1
F33E11.6b.1
F33E11.6c.1
Other_sequenceTcir_isotig01329
Dviv_isotig07152
Dviv_isotig07150
Hbac_isotig07261
ES561532.1
Associated_feature (14)
Experimental_infoRNAi_resultWBRNAi00046213Inferred_automaticallyRNAi_primary
WBRNAi00046214Inferred_automaticallyRNAi_primary
WBRNAi00116274Inferred_automaticallyRNAi_primary
WBRNAi00116275Inferred_automaticallyRNAi_primary
Expr_patternExpr1016210
Expr1037760
Expr1150100
Expr2014890
Expr2033125
Microarray_results (25)
Expression_cluster (142)
InteractionWBInteraction000388307
WBInteraction000388308
WBInteraction000559252
WBInteraction000561251
WBInteraction000568762
WBInteraction000569737
WBInteraction000574915
Map_infoMapVPosition-20.0045
PositivePositive_cloneF33E11Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00041771
WBPaper00046494
WBPaper00055090
WBPaper00062514
WBPaper00063737
WBPaper00065308
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