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WormBase Tree Display for Gene: WBGene00001132

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Name Class

WBGene00001132SMapS_parentSequenceCHROMOSOME_IV
IdentityVersion2
NameCGC_namealp-1Person_evidenceWBPerson910
Sequence_nameT11B7.4
Molecular_name (15)
Other_nameCELE_T11B7.4Accession_evidenceNDBBX284604
Public_namealp-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:23WBPerson1971EventImportedInitial conversion from geneace
216 Jan 2006 17:50:31WBPerson2970Name_changeCGC_namealp-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classalp
Allele (152)
StrainWBStrain00035455
WBStrain00035457
WBStrain00031648
RNASeq_FPKM (74)
GO_annotation (34)
Ortholog (60)
ParalogWBGene00014262Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionalp-1 encodes the C. elegans ortholog of the ALP (alpha-actininassociated LIM protein)-Enigma family of proteins that are found at sites of actin filament anchorage, such as the muscle Z disk; in C. elegans, alp-1 is required for maintenance of actin filament organization and for stabilizing muscle contraction; ALP-1 co-localizes with alpha-actinin at body wall muscle dense bodies, and its localization is dependent upon alpha-actinin.Paper_evidenceWBPaper00032968
Curator_confirmedWBPerson1843
WBPerson324
WBPerson567
Date_last_updated16 Jul 2009 00:00:00
Automated_descriptionPredicted to enable actin binding activity and muscle alpha-actinin binding activity. Involved in determination of adult lifespan and pharyngeal pumping. Located in several cellular components, including actin filament bundle; basal part of cell; and striated muscle dense body. Expressed in body wall musculature; hypodermis; marginal cell; and pharyngeal muscle cell. Used to study cardiomyopathy and myopathy. Human ortholog(s) of this gene implicated in dilated cardiomyopathy 1C; distal myopathy; myofibrillar myopathy 4; and myotonic dystrophy type 1. Is an ortholog of human PDLIM5 (PDZ and LIM domain 5).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:423Homo sapiensPaper_evidenceWBPaper00032968
Accession_evidenceOMIM609452
Curator_confirmedWBPerson324
Date_last_updated09 Oct 2018 00:00:00
DOID:0050700Homo sapiensPaper_evidenceWBPaper00032968
Accession_evidenceOMIM601493
Curator_confirmedWBPerson324
Date_last_updated03 Oct 2018 00:00:00
Potential_modelDOID:11720Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:15710)
DOID:12930Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:15710)
DOID:0080095Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:15710)
DOID:0110423Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:15710)
DOID:11722Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:15710)
Disease_relevanceMuscular dystrophies are a group of hereditary muscle diseases characterized by progressive muscle weakness; several proteins including the ALP (alpha-actinin-associated LIM protein)-Enigma proteins, a group of evolutionarily conserved proteins localized at the Z-disk and other sites of actin filament anchorage, are implicated in myopathies; though alp-1 mutant worms have grossly normal muscle function they show an alteration in action filaments in body wall muscle, exhibiting small actin aggregates at the ends of muscle.Homo sapiensPaper_evidenceWBPaper00032968
WBPaper00026945
Accession_evidenceOMIM601493
609452
605906
Curator_confirmedWBPerson324
Date_last_updated30 Apr 2015 00:00:00
Models_disease_assertedWBDOannot00000283
WBDOannot00000319
Molecular_infoCorresponding_CDST11B7.4a
T11B7.4b
T11B7.4c
T11B7.4d
T11B7.4e
Corresponding_CDS_historyT11B7.4b:wp112
Corresponding_transcriptT11B7.4a.1
T11B7.4b.1
T11B7.4c.1
T11B7.4d.1
T11B7.4e.1
Other_sequence (68)
Associated_featureWBsf660454
WBsf660455
WBsf660456
WBsf716784
WBsf228749
WBsf228750
Experimental_infoRNAi_resultWBRNAi00009156Inferred_automaticallyRNAi_primary
WBRNAi00080557Inferred_automaticallyRNAi_primary
WBRNAi00002262Inferred_automaticallyRNAi_primary
WBRNAi00079868Inferred_automaticallyRNAi_primary
WBRNAi00018585Inferred_automaticallyRNAi_primary
WBRNAi00001688Inferred_automaticallyRNAi_primary
WBRNAi00075890Inferred_automaticallyRNAi_primary
WBRNAi00035468Inferred_automaticallyRNAi_primary
WBRNAi00053101Inferred_automaticallyRNAi_primary
WBRNAi00053102Inferred_automaticallyRNAi_primary
Expr_patternChronogram792
Expr3919
Expr3920
Expr6672
Expr8651
Expr1013432
Expr1030722
Expr1156707
Expr2009313
Expr2027549
Drives_constructWBCnstr00001767
WBCnstr00001768
WBCnstr00003383
WBCnstr00037071
Construct_productWBCnstr00001766
WBCnstr00001767
WBCnstr00001768
WBCnstr00016198
WBCnstr00037071
AntibodyWBAntibody00001942
WBAntibody00001943
Microarray_results (42)
Expression_cluster (209)
Interaction (375)
Map_infoPositivePositive_cloneT11B7Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_data2_point4247
4450
5205
5526
5527
Multi_point1535
1537
1612
1832
1922
1876
Pos_neg_data4244
4245
4246
4451
4452
4647
4648
4649
4650
4651
Interpolated_map_positionIV3.98591
Reference (29)
Remarkeat-1 was previously connected to T11B7.4 based on findings described in WBPaper00018820, WBPaper00012350 & WBPaper00017849. It has subsequently been found that these results were incorrect. The correct eat-1 object can be found in WBGene00044731Person_evidenceWBPerson910
Curator_confirmedWBPerson2970
MethodGene