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WormBase Tree Display for Gene: WBGene00003515

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Name Class

WBGene00003515SMapS_parentSequenceK12F2
IdentityVersion1
NameCGC_namemyo-3Person_evidenceWBPerson261
Sequence_nameK12F2.1
Molecular_nameK12F2.1
K12F2.1.1
CE34936
Other_namesup-3
CELE_K12F2.1Accession_evidenceNDBBX284605
Public_namemyo-3
DB_infoDatabaseAceViewgene5M708
WormQTLgeneWBGene00003515
WormFluxgeneWBGene00003515
NDBlocus_tagCELE_K12F2.1
PanthergeneCAEEL|WormBase=WBGene00003515|UniProtKB=P12844
familyPTHR45615
NCBIgene179676
RefSeqproteinNM_073664.7
SwissProtUniProtAccP12844
UniProt_GCRPUniProtAccP12844
OMIMgene160710
160720
160740
160741
160760
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:32WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classmyo
AlleleWBVar00248743Inferred_automaticallyFrom strain object: MAH19
From strain object: RW1596
From strain object: RW3538
WBVar00248715
WBVar00088652
WBVar00088597
WBVar00088653
WBVar00143980
WBVar00088596
WBVar00143982
WBVar00143966
WBVar00248741
WBVar00088602
WBVar00248774
WBVar00088622
WBVar00088595
WBVar00248714
WBVar00241759
WBVar00088651
WBVar00248776
WBVar01866885
WBVar01866886
WBVar01866887
WBVar01866888
WBVar01499547
WBVar01053628
WBVar00304602
WBVar01053629
WBVar01053630
WBVar01053631
WBVar01053632
WBVar01053633
WBVar01053634
WBVar01053635
WBVar01053636
WBVar01053637
WBVar01053638
WBVar01053639
WBVar01053640
WBVar01053641
WBVar01053642
WBVar01053643
WBVar01053644
WBVar01743649
WBVar01053645
WBVar01743650
WBVar01053646
WBVar01053647
WBVar01053648
WBVar01053649
WBVar01053650
WBVar01053651
WBVar00066030
WBVar01053652
WBVar00472338
WBVar01053653
WBVar00472339
WBVar01053654
WBVar01053655
WBVar00472340
WBVar01053656
WBVar00472341
WBVar00472342
WBVar01053657
WBVar01053658
WBVar00472343
WBVar01053659
WBVar00472344
WBVar00472345
WBVar01053660
WBVar00472346
WBVar01053661
WBVar00472347
WBVar01053662
WBVar00472348
WBVar01053663
WBVar00472349
WBVar01053664
WBVar01053665
WBVar00472350
WBVar01053666
WBVar00472351
WBVar01053667
WBVar00472352
WBVar01053668
WBVar00472353
WBVar01053669
WBVar00472354
WBVar00472355
WBVar01053670
WBVar01053671
WBVar00472356
WBVar00472357
WBVar01053672
WBVar00472358
WBVar01053673
WBVar01053674
WBVar00472359
WBVar00472360
WBVar01053675
WBVar00472361
WBVar01053676
WBVar01053677
WBVar00472362
WBVar00472363
WBVar01053678
WBVar00472364
WBVar01053679
WBVar01053680
WBVar00472365
WBVar01053681
WBVar01053682
WBVar01053683
WBVar01053684
WBVar00006955
WBVar01500212
WBVar01500213
WBVar00006960
WBVar01499299
WBVar01661227
WBVar01484767
WBVar02061308
WBVar01499316
Legacy_informationStructural gene for minor body-wall myosin heavy chain. Mutation st378 is probable null for myo-3 : late embryonic lethal very abnormal muscle ultrastructure. See also sup-3.
e1407sd : partial suppressor of certain mutations of muscle genes unc-15 unc-54 unc-87 e.g. unc-15(e73) unc-54(e1315); no phenotype alone; may be associated with alteration of minor body wall myosin gene myo-3 V and causes increased levels of myo-3 product. Deficiency eDf1 has sup-3 activity. ES3 in presence of e73 ME3. NA > 10 (e1390 etc.). Also super-suppressor alleles (unstable) and antisuppressor alleles derived from e1407 etc.
See also e1390, e1405, e1407, m139, m141, m148, m157, m207, s196, st90, st92
[Williams BD] Pat (paralysed arrest at two-fold), severe paralysis.
[C.elegansII] st386 : severe Pat (paralysed embryonic arrest at two-fold stage); very abnormal muscle ultrastructure, no MYO-3 staining.OA2 (Pat): st563, st565. Also duplication alleles: e1407sd(pka sup-3, partial suppressor of certain mutations of muscle genes unc-15, unc-54, unc-87), e1390, etc.; Also super-suppressor alleles (unstable). All probably tandem duplications or further amplifications of myo-3. [Dibb et al. 1989; Maruyama et al. 1989; Williams and Waterston 1989]
Strain (34)
RNASeq_FPKM (74)
GO_annotation (31)
Ortholog (80)
Paralog (21)
Structured_descriptionConcise_descriptionmyo-3 encodes MHC A, the minor isoform of MHC (myosin heavy chain) that is essential for thick filament formation, and for viability, movement, and embryonic elongation; expressed in body muscle, the somatic sheath cell covering the hermaphrodite gonad, and also expressed in enteric muscle, vulval muscles of the hermaphrodite and the diagonal muscles of the male tail.Paper_evidence (11)
Curator_confirmedWBPerson48
Date_last_updated21 Jan 2005 00:00:00
Automated_descriptionEnables cytoskeletal motor activity. Involved in locomotory behavior and positive regulation of ovulation. Located in A band and striated muscle myosin thick filament. Expressed in body wall musculature; enteric muscle; gonad; vulval muscle; and in male. Human ortholog(s) of this gene implicated in several diseases, including congenital heart disease (multiple); distal myopathy 1; and intrinsic cardiomyopathy (multiple). Is an ortholog of several human genes including MYH1 (myosin heavy chain 1); MYH2 (myosin heavy chain 2); and MYH3 (myosin heavy chain 3).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 (30)
Molecular_infoCorresponding_CDSK12F2.1
Corresponding_CDS_historyK12F2.1:wp106
Corresponding_transcriptK12F2.1.1
Other_sequence (194)
Associated_feature (11)
Experimental_infoRNAi_result (11)
Expr_pattern (14)
Drives_construct (391)
Construct_productWBCnstr00009392
WBCnstr00019120
WBCnstr00021706
WBCnstr00036079
AntibodyWBAntibody00000014
WBAntibody00000019
WBAntibody00000391
WBAntibody00001784
Microarray_resultsSMD_K12F2.1
191856_s_at
A_12_P102403
Aff_K12F2.1
GPL13394_WBGene00003515
GPL13914_K12F2.1
GPL14144_K12F2.1_4635-4694_0.827_84_B
GPL14144_K12F2.1_4799-4858_0.762_321_A
GPL14144_K12F2.1_5752-5811_0.924_9_C
GPL19516_CGZ0029381
GPL21109_K12F2.1
GPL3518_CE12204
GPL8304_CE_WBGene00003515_A
GPL8673_K12F2_1P04511
GPL8673_K12F2_1P05176
GPL8673_K12F2_1P05774
GPL9450_K12F2.1
cea2.p.121524
Expression_cluster (285)
Interaction (183)
WBProcessWBbiopr:00000006
WBbiopr:00000040
Map_infoMapVPosition3.84005Error0.021073
Well_ordered
PositivePositive_cloneK12F2Inferred_automaticallyFrom sequence, transcript, pseudogene data
SG25/35
Mapping_data2_point141
315
3133
3134
Multi_point148
782
1176
1177
1178
2809
2817
5284
Pos_neg_data300
3135
854
866
Reference (284)
RemarkData extracted from Williams & Waterston 1994
yk1d8.5,yk1d8.3, removed from sequence list sdm 11/00
MethodGene