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WormBase Tree Display for Gene: WBGene00001056

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Name Class

WBGene00001056EvidencePerson_evidenceWBPerson2549
WBPerson6733
SMapS_parentSequenceK02F2
IdentityVersion1
NameCGC_namedpf-3
Sequence_nameK02F2.1
Molecular_nameK02F2.1a
K02F2.1a.1
CE17153
K02F2.1b
CE28837
K02F2.1b.1
Other_nameK02F2.aCurator_confirmedWBPerson1983
RemarkOld cosmid naming mapped via unique overlapping PCR_product on CDSs
K02F2.iCurator_confirmedWBPerson1983
RemarkOld cosmid naming mapped via unique overlapping PCR_product on CDSs
CELE_K02F2.1Accession_evidenceNDBBX284601
Public_namedpf-3
DB_infoDatabaseAceViewgene1H419
WormQTLgeneWBGene00001056
WormFluxgeneWBGene00001056
NDBlocus_tagCELE_K02F2.1
PanthergeneCAEEL|WormBase=WBGene00001056|UniProtKB=H2KZK7
familyPTHR11731
NCBIgene172409
RefSeqproteinNM_059555.2
NM_059556.5
TrEMBLUniProtAccQ965K3
H2KZK7
UniProt_GCRPUniProtAccH2KZK7
OMIMgene608258
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:22WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classdpf
Allele (51)
RNASeq_FPKM (74)
GO_annotation00022369
00022370
00108173
00108174
Contained_in_operonCEOP1999
Ortholog (45)
ParalogWBGene00001054Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00001055Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00001057Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001058Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001059Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable dipeptidyl-peptidase activity. Predicted to be involved in proteolysis. Human ortholog(s) of this gene implicated in primary immunodeficiency disease. Is an ortholog of human DPP8 (dipeptidyl peptidase 8) and DPP9 (dipeptidyl peptidase 9).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:612Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18648)
Molecular_infoCorresponding_CDSK02F2.1a
K02F2.1b
Corresponding_transcriptK02F2.1a.1
K02F2.1b.1
Other_sequence (30)
Associated_featureWBsf643404
WBsf656448
WBsf656449
WBsf976760
WBsf976761
WBsf976762
WBsf976763
WBsf217906
WBsf217907
Experimental_infoRNAi_resultWBRNAi00003898Inferred_automaticallyRNAi_primary
WBRNAi00116484Inferred_automaticallyRNAi_primary
WBRNAi00062300Inferred_automaticallyRNAi_primary
WBRNAi00049733Inferred_automaticallyRNAi_primary
WBRNAi00089105Inferred_automaticallyRNAi_primary
WBRNAi00033886Inferred_automaticallyRNAi_primary
Expr_patternExpr1015335
Expr1030666
Expr1153455
Expr2011041
Expr2029278
Drives_constructWBCnstr00037114
Construct_productWBCnstr00037114
Microarray_results (26)
Expression_cluster (131)
SAGE_tag (23)
Interaction (27)
Map_infoMapIPosition1.36995Error0.002958
PositivePositive_cloneK02F2Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00010074
WBPaper00019587
WBPaper00029387
WBPaper00038491
WBPaper00055090
WBPaper00061547
WBPaper00064339
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