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WormBase Tree Display for Gene: WBGene00003039

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Name Class

WBGene00003039SMapS_parentSequenceF56A12
IdentityVersion3
NameCGC_namemir-48Paper_evidenceWBPaper00026781
Person_evidenceWBPerson18
Sequence_nameF56A12.3
Molecular_nameF56A12.3
F56A12.3a
F56A12.3b
Other_namelin-58Person_evidenceWBPerson261
Cel-Let-7-P6RemarkMirGeneDB 2.1 import
CELE_F56A12.3Accession_evidenceNDBBX284605
Public_namemir-48
DB_infoDatabasemiRBaseaccMI0000019
SignaLinkmirnacel-mir-48
MirGeneDBcelCel-Let-7-P6
NDBlocus_tagCELE_F56A12.3
NCBIgene260115
RefSeqproteinNR_000793.2
RNAcentralURSidURS000000076D
URS00001CC103
URS000031C21C
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:30WBPerson1971EventImportedInitial conversion from geneace
219 Dec 2005 15:11:14WBPerson2970EventAcquires_mergeWBGene00003276
Name_changeSequence_nameF56A12.3
Other_namemir-48
325 Apr 2016 10:28:20WBPerson2970Name_changeCGC_namemir-48
Other_namelin-58
Acquires_mergeWBGene00003276
StatusLive
Gene_infoBiotypeSO:0001265
Gene_classmir
Allele (13)
Legacy_information[Abrahante JE, Miller EA, Rougvie AE] Both alleles produce precocious adult alae, at L3-to-L4 molt. Less distinct that precocious alae in lin-14(lf). ve33 stronger allele, semidominant. Mutations identified as suppressors of lin-4 suppression of col-19::GFP, veIs13 reporter.
StrainWBStrain00027436
WBStrain00027438
WBStrain00040222
WBStrain00051626
WBStrain00051625
In_clusterLET-7
RNASeq_FPKM (74)
GO_annotation00106183
00106184
00106185
Structured_descriptionConcise_descriptionmir-48 encodes a microRNA (miRNA); mir-48 was identified in screens for new heterochronic loci required for the proper temporal control of specific postembryonic cell divisions; mutations in mir-48 result in precocious terminal differentiation of hypodermal seam cells and secretion of adult cuticle one stage too early.Paper_evidenceWBPaper00003119
WBPaper00026781
Curator_confirmedWBPerson1843
Date_last_updated11 Jul 2007 00:00:00
Automated_descriptionInvolved in miRNA-mediated gene silencing by inhibition of translation and positive regulation of development, heterochronic. Expressed in P5.p hermaphrodite; P7.p hermaphrodite; RID; and seam cell. Used to study Parkinson's disease.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_infoExperimental_modelDOID:14330Homo sapiensPaper_evidenceWBPaper00035654
Curator_confirmedWBPerson324
Date_last_updated06 Jan 2014 00:00:00
Disease_relevancemir-48 is a small non-protein coding RNA that belongs to the let-7 family; microRNA expression profiling studies in an elegans transgenic model of Parkinson''s disease, where A53T alpha-synuclein is overexpressed, indicate that elegans mir-48 and mir-84 are underexpressed; also mir-48 is underexpressed in a pdr-1 mutant; pdr-1 is orthologous to human PARKIN, which is associated with the juvenile form of Parkinson disease, adenocarcinomas of the ovary and lung, and susceptibility to Leprosy.Homo sapiensPaper_evidenceWBPaper00035654
Curator_confirmedWBPerson324
Date_last_updated06 Jan 2014 00:00:00
Models_disease_in_annotationWBDOannot00000263
Molecular_infoCorresponding_transcriptF56A12.3
F56A12.3a
F56A12.3b
Associated_featureWBsf034323
WBsf979127
WBsf1001988
WBsf1001989
WBsf1001990
WBsf1020826
WBsf1020827
Experimental_infoExpr_pattern (11)
Drives_constructWBCnstr00004855
WBCnstr00004856
WBCnstr00004857
WBCnstr00004858
WBCnstr00005523
WBCnstr00011650
WBCnstr00020505
Construct_productWBCnstr00004855
WBCnstr00004856
WBCnstr00004857
WBCnstr00004858
WBCnstr00016932
Expression_cluster (30)
Interaction (23)
WBProcessWBbiopr:00000083
Map_infoMapVPosition6.27549Error0.003412
PositiveInside_rearryDf8
nDf51
Positive_cloneF56A12Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
NegativeOutside_rearryDf4
Mapping_dataMulti_point3706
5653
Pos_neg_data9420
9421
10749
Reference (86)
RemarkData extracted from Abrahante et al. (1998)
Rfam accession number: MI0000019
MethodGene