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WormBase Tree Display for Gene: WBGene00016200

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Name Class

WBGene00016200SMapS_parentSequenceC28H8
IdentityVersion2
NameCGC_namedpff-1Person_evidenceWBPerson260
Sequence_nameC28H8.9
Molecular_nameC28H8.9a
C28H8.9a.1
CE06896
C28H8.9b
CE32813
C28H8.9c
CE41615
C28H8.9b.1
C28H8.9c.1
Other_nameCELE_C28H8.9Accession_evidenceNDBBX284603
Public_namedpff-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:57WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
214 Oct 2011 15:24:19WBPerson2970Name_changeCGC_namedpff-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classdpff
Allele (42)
StrainWBStrain00034996
WBStrain00034997
WBStrain00054717
RNASeq_FPKM (74)
GO_annotation (12)
Ortholog (45)
ParalogWBGene00007029Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00007914Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00018013Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00016200Caenorhabditis elegansFrom_analysisInparanoid_8
WBGene00045419Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00010537Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable metal ion binding activity. Involved in apoptotic process; meiotic cell cycle; and response to heat. Located in nucleus. Expressed widely. Used to study alcohol use disorder. Human ortholog(s) of this gene implicated in Coffin-Siris syndrome 7. Is an ortholog of human DPF2 (double PHD fingers 2) and DPF3 (double PHD fingers 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_infoExperimental_modelDOID:1574Homo sapiensPaper_evidenceWBPaper00046494
Curator_confirmedWBPerson324
Date_last_updated20 May 2019 00:00:00
Potential_modelDOID:0112369Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9964)
Models_disease_assertedWBDOannot00000673
Molecular_infoCorresponding_CDSC28H8.9a
C28H8.9b
C28H8.9c
Corresponding_transcriptC28H8.9a.1
C28H8.9b.1
C28H8.9c.1
Other_sequence (48)
Associated_featureWBsf651084
WBsf992568
WBsf992569
WBsf992570
WBsf992571
WBsf1014978
WBsf1014979
Transcription_factorWBTranscriptionFactor000660
Experimental_infoRNAi_resultWBRNAi00005310Inferred_automaticallyRNAi_primary
WBRNAi00029308Inferred_automaticallyRNAi_primary
WBRNAi00011317Inferred_automaticallyRNAi_primary
WBRNAi00113485Inferred_automaticallyRNAi_primary
WBRNAi00041436Inferred_automaticallyRNAi_primary
WBRNAi00115785Inferred_automaticallyRNAi_primary
Expr_patternExpr13521
Expr1016807
Expr1036933
Expr1145465
Expr1200281
Expr1200282
Expr2011046
Expr2029283
Drives_constructWBCnstr00028250
Construct_productWBCnstr00016602
WBCnstr00021804
WBCnstr00028250
Microarray_results (29)
Expression_cluster (85)
Interaction (37)
Map_infoMapIIIPosition-1.43608Error0.000668
PositivePositive_cloneC28H8Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00043688
WBPaper00046494
WBPaper00053111
WBPaper00055090
WBPaper00056971
WBPaper00061738
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