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WormBase Tree Display for Gene: WBGene00007753

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Name Class

WBGene00007753SMapS_parentSequenceC27A7
IdentityVersion2
NameCGC_nameenpp-1Person_evidenceWBPerson44
WBPerson55385
Sequence_nameC27A7.1
Molecular_name (12)
Other_nameCELE_C27A7.1Accession_evidenceNDBBX284605
Public_nameenpp-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:48WBPerson1971EventImportedInitial conversion from CDS class of WS125
209 Dec 2021 11:50:30WBPerson1983Name_changeCGC_nameenpp-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classenpp
Allele (100)
RNASeq_FPKM (74)
GO_annotation00008083
00048966
00048967
00048968
00048969
Ortholog (39)
ParalogWBGene00007755Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00008776Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00015283Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00020195Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionC27A7.1 is orthologous to the human gene NPPASE (ENPP1; OMIM:173335), which when mutated leads to disease.Curator_confirmedWBPerson1823
WBPerson567
Date_last_updated06 Aug 2004 00:00:00
Automated_descriptionPredicted to enable hydrolase activity. Predicted to be located in I band and striated muscle dense body. Expressed in ciliated neurons; pharynx; and vas deferens cuboidal cell. Human ortholog(s) of this gene implicated in several diseases, including arterial calcification of infancy; end stage renal disease; and ossification of the posterior longitudinal ligament of spine. Is an ortholog of human ENPP1 (ectonucleotide pyrophosphatase/phosphodiesterase 1); ENPP2 (ectonucleotide pyrophosphatase/phosphodiesterase 2); and ENPP3 (ectonucleotide pyrophosphatase/phosphodiesterase 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_infoPotential_modelDOID:0050644Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3356)
DOID:9352Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3356)
EFO:MONDO:0000044Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3356)
DOID:783Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3356)
DOID:3068Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3356)
DOID:13207Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3357)
DOID:0060887Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3356)
DOID:1287Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3356)
DOID:9970Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3356)
Molecular_infoCorresponding_CDSC27A7.1a
C27A7.1b
C27A7.1c
C27A7.1d
Corresponding_transcriptC27A7.1a.1
C27A7.1b.1
C27A7.1c.1
C27A7.1d.1
Other_sequenceEX014395.1
AI581477.1
JI245909.1
OVC00626_1
JI165437.1
CBC15576_1
HBC20340_1
Associated_featureWBsf1001523
WBsf1020536
WBsf232608
Experimental_infoRNAi_resultWBRNAi00029253Inferred_automaticallyRNAi_primary
WBRNAi00041308Inferred_automaticallyRNAi_primary
WBRNAi00056472Inferred_automaticallyRNAi_primary
WBRNAi00108542Inferred_automaticallyRNAi_primary
WBRNAi00011234Inferred_automaticallyRNAi_primary
WBRNAi00108617Inferred_automaticallyRNAi_primary
Expr_patternExpr15981
Expr15982
Expr15983
Expr1013891
Expr1033357
Expr1145350
Expr2001153
Expr2019374
Drives_constructWBCnstr00033508
WBCnstr00042633
Construct_productWBCnstr00033508
WBCnstr00042633
Microarray_results (26)
Expression_cluster (152)
Interaction (14)
Map_infoPositivePositive_cloneC27A7Inferred_automaticallyFrom sequence, transcript, pseudogene data
Interpolated_map_positionV3.66987
ReferenceWBPaper00038491
WBPaper00042257
WBPaper00055090
WBPaper00062669
WBPaper00065330
MethodGene