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WormBase Tree Display for Gene: WBGene00017393

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Name Class

WBGene00017393SMapS_parentSequenceF12A10
IdentityVersion2
NameCGC_namenep-5Person_evidenceWBPerson260
Sequence_nameF12A10.4
Molecular_nameF12A10.4
F12A10.4.1
CE54011
Other_nameCELE_F12A10.4Accession_evidenceNDBBX284602
Public_namenep-5
DB_infoDatabaseAceViewgene2F779
WormQTLgeneWBGene00017393
WormFluxgeneWBGene00017393
NDBlocus_tagCELE_F12A10.4
PanthergeneCAEEL|WormBase=WBGene00017393|UniProtKB=Q09946
familyPTHR11733
NCBIgene173933
RefSeqproteinNM_001377801.1
TrEMBLUniProtAccQ09946
UniProt_GCRPUniProtAccQ09946
OMIMgene605896
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:58WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
210 Feb 2012 15:49:10WBPerson2970Name_changeCGC_namenep-5
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classnep
Allele (39)
StrainWBStrain00033134
RNASeq_FPKM (74)
GO_annotation (12)
Ortholog (94)
Paralog (24)
Structured_descriptionConcise_descriptionF12A10.4 encodes a neprilysin; neprilysins are thermolysin-like zinc metallopeptidases, found on the outer surface of animal cells, that negatively regulate small signalling peptides (e.g., enkephalin, tachykinin, insulin, and natriuretic peptides) by cleaving them; F12A10.4 has no clear orthologs in other organisms.Paper_evidenceWBPaper00004584
WBPaper00013276
Curator_confirmedWBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable metalloendopeptidase activity. Predicted to be involved in protein processing. Predicted to be located in plasma membrane. Human ortholog(s) of this gene implicated in distal arthrogryposis type 5D. Is an ortholog of human ECEL1 (endothelin converting enzyme like 1) and KEL (Kell metallo-endopeptidase (Kell blood group)).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:0111594Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3147)
Molecular_infoCorresponding_CDSF12A10.4
Corresponding_CDS_historyF12A10.4:wp228
F12A10.4:wp274
Corresponding_transcriptF12A10.4.1
Other_sequenceCR03396
CRC04115_1
Associated_featureWBsf987896
WBsf1012233
Experimental_infoRNAi_resultWBRNAi00013155Inferred_automaticallyRNAi_primary
WBRNAi00044425Inferred_automaticallyRNAi_primary
WBRNAi00001260Inferred_automaticallyRNAi_primary
WBRNAi00089036Inferred_automaticallyRNAi_primary
WBRNAi00030849Inferred_automaticallyRNAi_primary
Expr_patternExpr1016375
Expr1148370
Expr2013973
Drives_constructWBCnstr00027331
Construct_productWBCnstr00027331
Microarray_results (18)
Expression_cluster (105)
InteractionWBInteraction000426992
WBInteraction000503131
Map_infoMapIIPosition-1.27871
PositivePositive_cloneF12A10Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00011735
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