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WormBase Tree Display for Gene: WBGene00001309

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Name Class

WBGene00001309SMapS_parentSequenceM01D7
IdentityVersion1
NameCGC_nameemr-1
Sequence_nameM01D7.6
Molecular_nameM01D7.6
M01D7.6.1
CE12270
M01D7.6.2
Other_nameCELE_M01D7.6Accession_evidenceNDBBX284601
Public_nameemr-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:24WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classemr
Allele (18)
StrainWBStrain00002843
WBStrain00035605
WBStrain00036376
WBStrain00003842
RNASeq_FPKM (74)
GO_annotation (14)
Contained_in_operonCEOP1992
Ortholog (12)
Structured_descriptionConcise_descriptionemr-1 gene encodes a homolog of the human integral nuclear membrane protein emerin ; EMR-1 belongs to a family of proteins sharing the LEM-domain (LAP2-Emerin-MAN1 domain) that are generally conserved in metazoa and bind to lamin; EMR-1, along with another LEM-domain protein, LEM-2 is required for larval development, normal life-span, nuclear envelope and chromatin organization, chromosome segregation and cell division; emr-1 is also required for smooth muscle activity; emr-1 negatively regulates pha-4, the transcription factor required for pharynx identity; EMR-1 protein is found in the nuclear envelopes of all cell types except sperm and at all life stages; EMR-1 binds to lamin/LMN-1; emr-1 mutations also exhibit weak hypersensitivity to DNA damage.Paper_evidenceWBPaper00004339
WBPaper00005158
WBPaper00005648
WBPaper00005828
WBPaper00040518
WBPaper00037040
WBPaper00040826
Curator_confirmedWBPerson48
WBPerson1843
WBPerson324
WBPerson567
Date_last_updated12 Apr 2012 00:00:00
Automated_descriptionEnables lamin binding activity. Involved in several processes, including mitotic cytokinesis; nuclear envelope organization; and response to X-ray. Located in nuclear inner membrane. Used to study Emery-Dreifuss muscular dystrophy. Is an ortholog of human LEMD1 (LEM domain containing 1).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:11726Homo sapiensPaper_evidenceWBPaper00044786
Accession_evidenceOMIM181350
Curator_confirmedWBPerson324
Date_last_updated09 Oct 2017 00:00:00
Disease_relevanceMutations in the human ortholog of emr-1, emerin, cause X-linked Emery-Dreifuss muscular dystrophy (EDMD); Emerin is a nuclear lamina protein and belongs to a family of LEM (LAP2-Emerin-MAN1) domain proteins that include MAN1, LEM2/NET25 and several others; LEM domain proteins bind lamin; mutations in human LMNA/lamin cause several laminopathic diseases including EDMD; much of the knowledge of the organization and assembly of the nuclear lamina has come from studies in elegans; studies in elegans have demonstrated the overlapping roles of emerin and lem-2 in embryogenesis, cell proliferation, lamin and heterochromatin organization; worm emerin and lem-2 are also involved in mitosis, smooth and striated muscle function, lifespan and meiotic progression, pointing to the many underlying processes that may affect disease phenotypes.Homo sapiensPaper_evidenceWBPaper00040268
Accession_evidenceOMIM310300
300384
Curator_confirmedWBPerson324
Date_last_updated01 Mar 2012 00:00:00
Models_disease_assertedWBDOannot00000045
Molecular_infoCorresponding_CDSM01D7.6
Corresponding_transcriptM01D7.6.1
M01D7.6.2
Other_sequenceGRC02002_1
GPC01900_1
CRC09112_1
CR02292
GP02519
CBC09681_1
Associated_featureWBsf982768
WBsf982769
WBsf217259
Experimental_infoRNAi_result (12)
Expr_pattern (13)
Drives_constructWBCnstr00000686
WBCnstr00000688
WBCnstr00003365
WBCnstr00018932
WBCnstr00020603
WBCnstr00020604
WBCnstr00020605
WBCnstr00037001
Construct_product (11)
Regulate_expr_clusterWBPaper00044786:emr-1(gk119)_downregulated
WBPaper00044786:emr-1(gk119)_upregulated
WBPaper00044786:emr-1(RNAi);lem-2(tm1582)_downregulated
WBPaper00044786:emr-1(RNAi);lem-2(tm1582)_upregulated
AntibodyWBAntibody00000305
WBAntibody00000306
WBAntibody00000307
WBAntibody00000597
WBAntibody00001856
WBAntibody00001941
Microarray_results (22)
Expression_cluster (149)
Interaction (84)
Map_infoMapIPosition-12.5332Error0.008453
PositivePositive_cloneM01D7Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point (2)
Pseudo_map_position
ReferenceWBPaper00004339
WBPaper00005158
WBPaper00005172
WBPaper00005637
WBPaper00005648
WBPaper00005828
WBPaper00017089
WBPaper00018156
WBPaper00024516
WBPaper00024687
WBPaper00025034
WBPaper00026102
WBPaper00026936
WBPaper00027235
WBPaper00027532
WBPaper00030590
WBPaper00035468
WBPaper00037040
WBPaper00038705
WBPaper00039053
WBPaper00040826
WBPaper00041279
WBPaper00042809
WBPaper00043784
WBPaper00044786
WBPaper00045548
WBPaper00046424
WBPaper00048885
WBPaper00051973
WBPaper00052385
WBPaper00059378
WBPaper00060526
WBPaper00061779
WBPaper00062371
WBPaper00064947
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