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WormBase Tree Display for Gene: WBGene00000832

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Name Class

WBGene00000832SMapS_parentSequenceY23H5A
IdentityVersion1
NameCGC_namectn-1Person_evidenceWBPerson481
Sequence_nameY23H5A.5
Molecular_name (12)
Other_nameY23H5A.cCurator_confirmedWBPerson1983
RemarkOld cosmid naming mapped via unique overlapping PCR_product on CDSs
CELE_Y23H5A.5Accession_evidenceNDBBX284601
Public_namectn-1
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:21WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classctn
Allele (245)
StrainWBStrain00037343
RNASeq_FPKM (74)
GO_annotation00021143
00021144
00021145
00021146
00021147
00021148
00107861
00107862
00107863
00107864
Ortholog (35)
ParalogWBGene00000942Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
WBGene00001978Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
Structured_descriptionConcise_descriptionctn-1 encodes a protein that belongs to the alpha-catulin family of catenin-like proteins; CTN-1 physically interacts in vivo with DYB-1/dystrobrevin; a ctn-1::GFP fusion is expressed in body wall, vulval, and anal muscles; in body wall muscles, CTN-1::GFP localizes to the plasma membranes near dense bodies.Paper_evidenceWBPaper00011358
WBPaper00041089
Curator_confirmedWBPerson1843
WBPerson324
Date_last_updated02 Aug 2012 00:00:00
Automated_descriptionPredicted to enable actin filament binding activity and cadherin binding activity. Involved in regulation of locomotion. Located in plasma membrane and striated muscle dense body. Expressed in body wall musculature; non-striated muscle; and somatic nervous system. Used to study Duchenne muscular dystrophy. Is an ortholog of human CTNNAL1 (catenin alpha like 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:11723Homo sapiensPaper_evidenceWBPaper00037625
Accession_evidenceOMIM310200
Curator_confirmedWBPerson324
Date_last_updated22 May 2017 00:00:00
Disease_relevanceMutations in human dystrophin are associated with the Duchenne and Becker types of muscular dystrophy, that affect skeletal muscles used for movement, and heart (cardiac) muscle; a number of transmembrane and peripheral membrane proteins interact with dystrophin to form the dystrophin-associated protein complex (DAPC); defects in components of the DAPC are associated with a variety of pathological conditions, including muscular dystrophy, cardiomyopathy, myoclonic dystonia, and vasospasm; in C. elegans, the DAPC localizes near dense bodies, structures that are analogous to muscle costameres; ctn-1, an ortholog of alpha catulin (catenin-like protein), interacts with dyb-1/dystrobrevin, and this interaction is required for the normal localization of the DAPC as well as for the slo-1 voltage- and calcium-activated potassium (BK) channel, in C. elegans muscle; in the dystrophic mdx mice, there is compensatory increase of alpha-catulin expression in the skeletal muscle where the DAPC is disassembled, and the mechanical link between the muscle costamere and the sarcolemma is lost.Homo sapiensPaper_evidenceWBPaper00037625
Curator_confirmedWBPerson324
Date_last_updated22 May 2017 00:00:00
Models_disease_assertedWBDOannot00000293
Molecular_infoCorresponding_CDSY23H5A.5a
Y23H5A.5c
Y23H5A.5d
Corresponding_CDS_historyY23H5A.5a:wp274
Y23H5A.5b:wp274
Y23H5A.5c:wp228
Y23H5A.5d:wp210
Y23H5A.5d:wp228
Corresponding_transcriptY23H5A.5e
Y23H5A.5a.1
Y23H5A.5c.1
Y23H5A.5d.1
Y23H5A.5d.2
Y23H5A.5d.3
Other_sequence (47)
Associated_featureWBsf982915
WBsf982916
WBsf1009363
WBsf217315
WBsf217316
Experimental_infoRNAi_resultWBRNAi00002350Inferred_automaticallyRNAi_primary
WBRNAi00055702Inferred_automaticallyRNAi_primary
WBRNAi00055701Inferred_automaticallyRNAi_primary
WBRNAi00116607Inferred_automaticallyRNAi_primary
WBRNAi00004565Inferred_automaticallyRNAi_primary
WBRNAi00022472Inferred_automaticallyRNAi_primary
WBRNAi00036720Inferred_automaticallyRNAi_primary
Expr_pattern (11)
Drives_constructWBCnstr00008299
WBCnstr00008300
WBCnstr00013721
WBCnstr00013723
WBCnstr00018330
WBCnstr00037258
Construct_productWBCnstr00008299
WBCnstr00008300
WBCnstr00008301
WBCnstr00008302
WBCnstr00013723
WBCnstr00013724
WBCnstr00018330
WBCnstr00020433
WBCnstr00037258
Microarray_results (51)
Expression_cluster (177)
Interaction (29)
Map_infoMapIPosition-8.18787Error0.026165
PositivePositive_cloneY23H5AInferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00011358
WBPaper00036762
WBPaper00037625
WBPaper00038491
WBPaper00039233
WBPaper00041089
WBPaper00043421
WBPaper00046703
WBPaper00055090
WBPaper00065040
RemarkSequence connection from [Broadbent ID], 02/06/12 krb.
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