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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_model (3)
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
ReferenceWBPaper00004416
WBPaper00005053
WBPaper00005158
WBPaper00005172
WBPaper00005648
WBPaper00005828
WBPaper00006526
WBPaper00018158
WBPaper00018364
WBPaper00024200
WBPaper00024687
WBPaper00024994
WBPaper00026640
WBPaper00026936
WBPaper00027235
WBPaper00027635
WBPaper00028456
WBPaper00028457
WBPaper00028870
WBPaper00030742
WBPaper00030942
WBPaper00031359
WBPaper00032468
WBPaper00032497
WBPaper00032926
WBPaper00033439
WBPaper00034662
WBPaper00035228
WBPaper00035468
WBPaper00036179
WBPaper00036840
WBPaper00038491
WBPaper00040258
WBPaper00041022
WBPaper00042684
WBPaper00043397
WBPaper00044786
WBPaper00045548
WBPaper00046801
WBPaper00047280
WBPaper00047337
WBPaper00047351
WBPaper00048885
WBPaper00049490
WBPaper00049828
WBPaper00051831
WBPaper00051949
WBPaper00051973
WBPaper00052327
WBPaper00055090
WBPaper00056325
WBPaper00057125
WBPaper00059378
WBPaper00060555
WBPaper00061687
WBPaper00061779
WBPaper00062371
WBPaper00062570
WBPaper00063084
WBPaper00064947
WBPaper00065000
WBPaper00065003
WBPaper00065308
WBPaper00065722
WBPaper00065928
WBPaper00066200
WBPaper00066275
RemarkSequence connection based on email from Wen
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