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WormBase Tree Display for Gene: WBGene00008656

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Name Class

WBGene00008656SMapS_parentSequenceF10F2
IdentityVersion2
NameCGC_namelron-5Person_evidenceWBPerson637
Sequence_nameF10F2.4
Molecular_nameF10F2.4
F10F2.4.1
CE31471
Other_nameCELE_F10F2.4Accession_evidenceNDBBX284603
Public_namelron-5
DB_infoDatabaseAceViewgene3F717
WormQTLgeneWBGene00008656
WormFluxgeneWBGene00008656
NDBlocus_tagCELE_F10F2.4
PanthergeneCAEEL|WormBase=WBGene00008656|UniProtKB=Q19312
familyPTHR45617
NCBIgene184307
RefSeqproteinNM_065542.6
TrEMBLUniProtAccQ19312
UniProt_GCRPUniProtAccQ19312
OMIMgene603288
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:49WBPerson1971EventImportedInitial conversion from CDS class of WS125
209 Dec 2011 15:47:23WBPerson2970Name_changeCGC_namelron-5
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classlron
Allele (38)
StrainWBStrain00047624
RNASeq_FPKM (74)
GO_annotation00064333
Ortholog (34)
Paralog (12)
Structured_descriptionAutomated_descriptionPredicted to be located in membrane. Expressed in nerve ring; tail; and ventral nerve cord. Human ortholog(s) of this gene implicated in several diseases, including artery disease (multiple); corneal disease (multiple); and periodontal disease (multiple). Is an ortholog of several human genes including FMOD (fibromodulin); LUM (lumican); and OMD (osteomodulin).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:3407Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6724)
DOID:11342Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6309)
DOID:0060287Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6309)
DOID:3087Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3774)
DOID:799Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6724)
DOID:10126Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6309)
DOID:1793Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6724)
DOID:3393Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6724)
DOID:2566Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6309)
DOID:824Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3774)
Molecular_infoCorresponding_CDSF10F2.4
Corresponding_CDS_historyF10F2.4:wp82
Corresponding_transcriptF10F2.4.1
Other_sequenceHCC07413_1
Dviv_isotig30850
HC05615
Oden_isotig24064
Associated_featureWBsf645108
WBsf224767
Experimental_infoRNAi_resultWBRNAi00001003Inferred_automaticallyRNAi_primary
WBRNAi00067524Inferred_automaticallyRNAi_primary
WBRNAi00044290Inferred_automaticallyRNAi_primary
WBRNAi00013073Inferred_automaticallyRNAi_primary
WBRNAi00005106Inferred_automaticallyRNAi_primary
WBRNAi00044289Inferred_automaticallyRNAi_primary
WBRNAi00030783Inferred_automaticallyRNAi_primary
Expr_patternChronogram928
Expr100
Expr5725
Expr9906
Expr1023550
Expr1033769
Expr1148237
Expr2013278
Expr2031509
Drives_constructWBCnstr00002901
WBCnstr00014392
WBCnstr00032794
Construct_productWBCnstr00014392
WBCnstr00032794
Microarray_results (19)
Expression_cluster (154)
InteractionWBInteraction000006978
WBInteraction000140266
WBInteraction000396162
WBInteraction000547733
Map_infoMapIIIPosition-2.9722
PositivePositive_cloneF10F2Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00060223
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