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WormBase Tree Display for Gene: WBGene00000539

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Name Class

WBGene00000539EvidenceCGC_data_submission
SMapS_parentSequenceF07B10
IdentityVersion1
NameCGC_namecln-3.1
Sequence_nameF07B10.1
Molecular_nameF07B10.1a
F07B10.1a.1
CE09198
F07B10.1b
CE46158
F07B10.1b.1
Other_nameCELE_F07B10.1Accession_evidenceNDBBX284605
Public_namecln-3.1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:21WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classcln
AlleleWBVar00239315Inferred_automaticallyFrom strain object: NL796
From strain object: XT4
From strain object: XT5
From strain object: XT7
WBVar02061002
WBVar02061003
WBVar00004020
WBVar00004025
WBVar01743453
WBVar01743454
WBVar01865645
WBVar01865646
WBVar01865647
WBVar01865648
WBVar02137107
WBVar00092929
WBVar00470337
WBVar00470338
WBVar00470339
WBVar01834618
WBVar01500208
WBVar01500209
WBVar01974797
WBVar01499299
WBVar01047671
WBVar01047672
WBVar01047673
WBVar01047674
WBVar01047675
WBVar01047676
WBVar01499316
WBVar01047677
WBVar01047678
WBVar01047679
WBVar01496926
WBVar01047680
WBVar01047681
WBVar01047682
WBVar01047683
WBVar01047684
WBVar01047685
StrainWBStrain00003257
WBStrain00028940
WBStrain00032172
WBStrain00040679
WBStrain00040680
WBStrain00040682
RNASeq_FPKM (74)
GO_annotation (15)
Ortholog (44)
ParalogWBGene00000540Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00007586
WBGene00000541Caenorhabditis elegansFrom_analysisInparanoid_8
Panther
WormBase-Compara
Structured_descriptionAutomated_descriptionInvolved in determination of adult lifespan and regulation of egg-laying behavior. Located in cytoplasm. Expressed in cuticle; diagonal muscle; hypodermis; intestine; and pharynx. Used to study neuronal ceroid lipofuscinosis. Human ortholog(s) of this gene implicated in neuronal ceroid lipofuscinosis 3. Is an ortholog of human CLN3 (CLN3 lysosomal/endosomal transmembrane protein, battenin).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:14503Homo sapiensPaper_evidenceWBPaper00027030
Accession_evidenceOMIM204200
Curator_confirmedWBPerson324
Date_last_updated08 May 2017 00:00:00
Potential_modelDOID:0110731Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2074)
Models_disease_assertedWBDOannot00000119
WBDOannot00000314
Molecular_infoCorresponding_CDSF07B10.1a
F07B10.1b
Corresponding_transcriptF07B10.1a.1
F07B10.1b.1
Other_sequence (13)
Associated_featureWBsf234521
Experimental_infoRNAi_resultWBRNAi00043854Inferred_automaticallyRNAi_primary
WBRNAi00030592Inferred_automaticallyRNAi_primary
Expr_patternChronogram53
Expr3817
Expr3818
Expr3819
Expr5669
Expr1023637
Expr1147829
Expr2010240
Expr2028482
Drives_constructWBCnstr00003732
WBCnstr00011674
WBCnstr00037464
Construct_productWBCnstr00037464
Microarray_results (19)
Expression_cluster (180)
InteractionWBInteraction000122588
WBInteraction000133974
WBInteraction000133975
WBInteraction000285465
WBInteraction000319652
WBInteraction000391919
WBInteraction000415645
Map_infoMapVPosition3.03495Error0.0019
PositivePositive_cloneF01B10
F07B10Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4225
4365
4855
4822
Pseudo_map_position
Reference (11)
Remark[Sara E Mole] Three C. elegans genes are equally similar to the human gene CLN3 which causes juvenile neuronal ceroid lipofuscinosis (NCL) or Batten disease. There is at least one similar gene in over 20 eukaryotic species, including S. cerevisiae, S.pombe, D. melanogaster. No other completely sequenced genome has more than one CLN3 homologue. All three cln-3 genes in C. elegans are trancribed and accession numbers have been applied for. In human there are up to 8 NCL genes named CLN-8. CLN1 also has one homologue in C. elegans. CLN1 encodes the enzyme palmitoyl protein thioesterase 1 (PPT1).
Map 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