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WormBase Tree Display for Gene: WBGene00003776

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Name Class

WBGene00003776SMapS_parentSequenceF52B10
IdentityVersion1
NameCGC_namenmy-1
Sequence_nameF52B10.1
Molecular_nameF52B10.1a
F52B10.1a.1
CE31177
F52B10.1b
CE04618
F52B10.1b.1
Other_nameCELE_F52B10.1Accession_evidenceNDBBX284606
Public_namenmy-1
DB_infoDatabaseAceViewgeneXD535
WormQTLgeneWBGene00003776
WormFluxgeneWBGene00003776
NDBlocus_tagCELE_F52B10.1
PanthergeneCAEEL|WormBase=WBGene00003776|UniProtKB=Q20641
familyPTHR45615
NCBIgene180581
RefSeqproteinNM_001374981.3
NM_076103.6
TrEMBLUniProtAccA0A5E4LXR0
Q20641
UniProt_GCRPUniProtAccQ20641
OMIMgene160745
160775
608568
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:32WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classnmy
Allele (107)
Legacy_information[C.elegansII] NMK. Encodes predicted non-muscle myosin heavy chain. [CGC]
[Newbern C] nmy for Non-Muscle Myosin.
StrainWBStrain00001168
WBStrain00008459
WBStrain00026590
RNASeq_FPKM (74)
GO_annotation (27)
Ortholog (59)
Paralog (21)
Structured_descriptionConcise_descriptionnmy-1 encodes a class II non-muscle myosin heavy chain related to Drosophila zipper, which plays a role in several aspects of embryonic morphogenesis; in C. elegans, NMY-1 is required for embryonic elongation and establishment of normal body morphology; however, nmy-1 functions redundantly with another non-muscle myosin heavy chain gene, nmy-2, during elongation and establishment of normal body morphology; mutations in nmy-1 suppress the hypercontraction phenotype produced by mutations in mel-11, a myosin phosphatase that regulates actomyosin filament contraction; in addition, NMY-1 may partner with MLC-4, myosin light chain 4, during elongation; NMY-1 expression is detected during embryogenesis, particularly at the onset of elongation.Paper_evidenceWBPaper00002905
WBPaper00005654
WBPaper00006149
WBPaper00013563
WBPaper00017143
WBPaper00019610
WBPaper00023409
Curator_confirmedWBPerson1843
WBPerson324
Date_last_updated11 Sep 2006 00:00:00
Automated_descriptionPredicted to enable actin filament binding activity and microfilament motor activity. Involved in several processes, including locomotion; nematode larval development; and regulation of embryonic cell shape. Located in adherens junction and contractile fiber. Expressed in head; hypodermis; and tail. Human ortholog(s) of this gene implicated in several diseases, including aortic aneurysm (multiple); auditory system disease (multiple); and blood platelet disease (multiple). Is an ortholog of human MYH11 (myosin heavy chain 11).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_infoPotential_model (14)
Molecular_infoCorresponding_CDSF52B10.1a
F52B10.1b
Corresponding_transcriptF52B10.1a.1
F52B10.1b.1
Other_sequence (63)
Associated_feature (17)
Experimental_infoRNAi_result (11)
Expr_patternChronogram1544
Expr2738
Expr6132
Expr1031765
Expr1151740
Expr2014340
Expr2032581
Drives_constructWBCnstr00002060
WBCnstr00035872
Construct_productWBCnstr00035872
AntibodyWBAntibody00000686
Microarray_results (16)
Expression_cluster (192)
Interaction (150)
Map_infoMapXPosition-12.6731Error0.002148
PositivePositive_cloneB0410Author_evidenceNewbern C
F52B10Author_evidenceNewbern C
Inferred_automaticallyFrom sequence, transcript, pseudogene data
Y76F7Author_evidenceNewbern C
Mapping_dataMulti_point5597
Pseudo_map_position
Reference (26)
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