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WormBase Tree Display for Gene: WBGene00003052

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Name Class

WBGene00003052SMapS_parentSequenceDY3
IdentityVersion1
NameCGC_namelmn-1
Sequence_nameDY3.2
Molecular_nameDY3.2
DY3.2.1
CE15746
Other_nameLam1Accession_evidenceEMBLX74027
CELE_DY3.2Accession_evidenceNDBBX284601
Public_namelmn-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:30WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classlmn
Allele (48)
StrainWBStrain00026339
WBStrain00026341
WBStrain00026343
WBStrain00040720
WBStrain00002790
WBStrain00026345
WBStrain00034808
Component_of_genotypeWBGenotype00000131
WBGenotype00000150
RNASeq_FPKM (74)
GO_annotation (36)
Ortholog (49)
Paralog (12)
Structured_descriptionConcise_descriptionlmn-1 encodes the sole C. elegans nuclear lamin; lmn-1 is an essential gene that is required for a number of nuclear processes, including chromatin organization, cell cycle progression, chromosome segregation, and nuclear pore complex spacing; LMN-1 is also required for nuclear envelope localization of EMR-1/Emerin during early development; LMN-1 localizes to the nuclear periphery of all cell types except sperm, and in embryonic and some adult cells is visible in the nuclear interior; LMN-1 binds mitotic chromosomes and histone H2A in a manner that requires its predicted nuclear localization signal, KRRR.Paper_evidenceWBPaper00004416
WBPaper00005158
WBPaper00028870
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated24 Feb 2009 00:00:00
Automated_descriptionEnables histone binding activity; identical protein binding activity; and structural molecule activity. Involved in several processes, including cellular localization; determination of adult lifespan; and regulation of cell cycle. Located in nuclear envelope and nuclear periphery. Expressed in several structures, including ventral cord blast cell. Used to study Emery-Dreifuss muscular dystrophy; congenital muscular dystrophy; and progeria. Human ortholog(s) of this gene implicated in several diseases, including Charcot-Marie-Tooth disease type 2B1; autosomal dominant Emery-Dreifuss muscular dystrophy 2; autosomal recessive Emery-Dreifuss muscular dystrophy 3; brain disease (multiple); congenital muscular dystrophy due to LMNA mutation; and intrinsic cardiomyopathy (multiple). Is an ortholog of human LMNA (lamin A/C).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:3911Homo sapiensPaper_evidenceWBPaper00032926
Curator_confirmedWBPerson38202
Date_last_updated24 May 2018 00:00:00
DOID:11726Homo sapiensPaper_evidenceWBPaper00040258
WBPaper00038510
Accession_evidenceOMIM181350
Curator_confirmedWBPerson324
Date_last_updated26 Jul 2023 00:00:00
DOID:0050557Homo sapiensPaper_evidenceWBPaper00040268
Curator_confirmedWBPerson324
Date_last_updated04 Feb 2013 00:00:00
Potential_model (25)
Models_disease_in_annotationWBDOannot00000297
Models_disease_assertedWBDOannot00000298
WBDOannot00000531
WBDOannot00000541
WBDOannot00001395
Molecular_infoCorresponding_CDSDY3.2
Corresponding_transcriptDY3.2.1
Other_sequence (14)
Associated_feature (18)
Experimental_infoRNAi_result (42)
Expr_pattern (13)
Drives_construct (13)
Construct_product (17)
Regulate_expr_clusterWBPaper00050182:lmn-1(L535P)_downregulated
WBPaper00050182:lmn-1(L535P)_upregulated
WBPaper00059378:lmn-1(Y59C)_downregulated
WBPaper00059378:lmn-1(Y59C)_upregulated
Antibody (13)
Microarray_results (23)
Expression_cluster (148)
Interaction (170)
Map_infoMapIPosition3.07104Error0.005882
PositivePositive_cloneDY3Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4741
Pseudo_map_position
Reference (67)
Remark (2)
MethodGene