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WormBase Tree Display for Gene: WBGene00008278

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Name Class

WBGene00008278SMapS_parentSequenceC53C7
IdentityVersion2
NameCGC_namenpr-10Paper_evidenceWBPaper00033064
Person_evidenceWBPerson42
Sequence_nameC53C7.1
Molecular_nameC53C7.1a
C53C7.1a.1
CE19767
C53C7.1b
CE36989
C53C7.1a.2
C53C7.1b.1
Other_nameCELE_C53C7.1Accession_evidenceNDBBX284606
Public_namenpr-10
DB_infoDatabaseAceViewgeneXN634
WormQTLgeneWBGene00008278
WormFluxgeneWBGene00008278
NDBlocus_tagCELE_C53C7.1
PanthergeneCAEEL|WormBase=WBGene00008278|UniProtKB=Q9XXU4
familyPTHR24235
NCBIgene183747
RefSeqproteinNM_001029316.4
NM_001029317.3
TrEMBLUniProtAccQ9XXU4
Q6EUU1
UniProt_GCRPUniProtAccQ9XXU4
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:48WBPerson1971EventImportedInitial conversion from CDS class of WS125
208 May 2009 14:29:51WBPerson9133Name_changeCGC_namenpr-10
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classnpr
Allele (231)
StrainWBStrain00032024
RNASeq_FPKM (74)
GO_annotation (16)
Ortholog (35)
Paralog (19)
Structured_descriptionAutomated_descriptionPredicted to enable neuropeptide binding activity and neuropeptide receptor activity. Predicted to be involved in G protein-coupled receptor signaling pathway. Predicted to be located in neuron projection and plasma membrane. Expressed in RMEV; ciliated neurons; and ganglia. Human ortholog(s) of this gene implicated in artery disease (multiple); lipid metabolism disorder; and obesity. Is an ortholog of human PRLHR (prolactin releasing hormone receptor).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:9970Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7958)
DOID:3146Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7958)
DOID:0050830Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7958)
DOID:10763Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4464)
Molecular_infoCorresponding_CDSC53C7.1a
C53C7.1b
Corresponding_transcriptC53C7.1a.1
C53C7.1a.2
C53C7.1b.1
Other_sequenceCJC11560_1
JI224784.1
FJ456886.1
Associated_featureWBsf1007503
WBsf1007504
WBsf1007505
WBsf1007506
WBsf1024171
WBsf238098
WBsf238099
Experimental_infoRNAi_resultWBRNAi00043087Inferred_automaticallyRNAi_primary
WBRNAi00030111Inferred_automaticallyRNAi_primary
WBRNAi00012357Inferred_automaticallyRNAi_primary
WBRNAi00072203Inferred_automaticallyRNAi_primary
Expr_patternExpr15833
Expr15834
Expr1018667
Expr1147052
Expr2014395
Expr2032636
Drives_constructWBCnstr00033090
WBCnstr00042540
Construct_productWBCnstr00033090
WBCnstr00042540
Microarray_results (22)
Expression_cluster (84)
InteractionWBInteraction000030160
WBInteraction000032037
WBInteraction000305389
WBInteraction000320874
WBInteraction000334023
WBInteraction000375442
WBInteraction000394749
WBInteraction000505876
WBInteraction000576912
Map_infoMapXPosition9.6717Error0.083925
PositivePositive_cloneC53C7Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00027520
WBPaper00038491
WBPaper00043908
WBPaper00055090
WBPaper00055865
WBPaper00061871
WBPaper00065946
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