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WormBase Tree Display for Gene: WBGene00006789

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Name Class

WBGene00006789SMapS_parentSequenceCHROMOSOME_I
IdentityVersion1
NameCGC_nameunc-54Person_evidenceWBPerson261
Sequence_nameF11C3.3
Molecular_nameF11C3.3
F11C3.3.1
CE09349
Other_name (2)
Public_nameunc-54
DB_infoDatabaseAceViewgene1P454
WormQTLgeneWBGene00006789
WormFluxgeneWBGene00006789
NDBlocus_tagCELE_F11C3.3
PanthergeneCAEEL|WormBase=WBGene00006789|UniProtKB=P02566
familyPTHR45615
NCBIgene259839
RefSeqproteinNM_061195.7
SwissProtUniProtAccP02566
UniProt_GCRPUniProtAccP02566
OMIMgene160710
160720
160740
160741
160760
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:42WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classunc
Allele (386)
Legacy_informationStructural gene for major body wall myosin heavy chain. Reference null allele e190 : limp paralysed phenotype at all stages larvae can move slightly more than adults Egl; muscle ultrastructure very disorganized few thick filaments. ES3 ME0. NA (recessive) > 50 including e1108amber; e1301ts; e675sd and s291 (in frame internal deletion mutants with heavy chain fragment behavioral phenotype almost paralysed slight twitcher); also Tc1 insertion mutants; etc. Also unusual suppressor alleles (NA > 15) e.g. s74 : dominant suppressor of unc-22(s12) no other dominant phenotype recessive phenotype slow stiff normal muscle ultrastructure; alteration in S1 portion of protein. Also Class 3 (dominant) alleles reference allele e1152sd : severe rigid paralysis small; e1152/+ paralysed weaker phenotype. ES3 ME0. NA (dominant) > 10 : e1153 n489 etc.; resemble e1152 or more severe recessive lethal. Intragenic revertants have Class 1 phenotypes.
See unc-54.
See also e569, e576, e651, e675, e843, e903, e1008, e1009, e1021, e1092, e1108, e1115, e1152, e1153, e1157, e1168, e1201, e1213, e1219, e1223, e1257, e1258, e1273, e1274, e1300, e1301, e1311, e1315, e1328, e1360, e1419, e1420, n325, n326, n327, n489, n794, r274, r308, r322, r323, r327, r360, s74, s75, s76, s77, s78, s95, s291, s409, s411
[C.elegansII] e190 : limp paralysed phenotype at all stages; larvae can move slightly more than adults; Egl; muscle ultrastructure very disorganized few thick filaments. ES3 ME0. OA>50 (recessive): e1108amb,e1301ts, e675sd and s291 (in frame internal deletion mutants, almost paralysed slight twitchers), etc. Also unusual suppressor alleles, OA>15: s74 (dominant suppressor of unc-22(s12), recessive slow, stiff; normal muscle ultrastructure) Also dominant antimorphic alleles, OA>10:e1152sd (severe rigid paralysis, small;e1152/+ paralysed weaker phenotype. ES3 ME0),r344 (recessive lethal, r344/+ severely paralysed), etc. Intragenic revertants have recessive paralysed phenotype. Some recessive alleles (r274, e1420 etc.) are dominant antimorphs in smg background. Cloned: encodes MHC B (MYO-4), major bodywall muscle myosin heavy chain. 6 kb message,1117 aa protein. Extensive molecular analysis. [Epstein et al. 1974; McLachlan and Karn 1982;Dibb et al. 1989; Bejsovec and Anderson 1990; TR; RW]
Strain (1380)
RNASeq_FPKM (74)
GO_annotation (31)
Ortholog (82)
Paralog (21)
Structured_descriptionConcise_descriptionunc-54 encodes a muscle myosin class II heavy chain (MHC B); UNC-54 is the major myosin heavy chain expressed in C. elegans and is required for locomotion and egg-laying; in vivo and in vitro, UNC-54 interacts with ITR-1, an IP3 receptor, and this interaction may provide a link between calcium signaling and the muscle cytoskeleton; UNC-54 is a thick filament component that is expressed in multiple muscle cell classes including body wall, intestinal, anal depressor, and sphincter muscles as well as sex-specific muscles that develop postembryonically.Paper_evidenceWBPaper00000232
WBPaper00000647
WBPaper00001014
WBPaper00005299
WBPaper00005940
Curator_confirmedWBPerson1843
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionEnables actin filament binding activity and microfilament motor activity. A structural constituent of muscle. Involved in several processes, including egg-laying behavior; muscle contraction; and skeletal muscle myosin thick filament assembly. Located in A band and striated muscle myosin thick filament. Part of muscle myosin complex. Expressed in anal depressor muscle; body wall musculature; head; 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_CDSF11C3.3
Corresponding_transcriptF11C3.3.1
Other_sequenceAS04147
SSC02445_1
OVC07502_1
FC811672.1
GO239982.1
FK804192.1
CD455920.1
GE637974.1
CK850816.1
MHC02251_1
AE04477
FC811340.1
SRC04394_1
GR978004.1
BMC04837_1
TSC00397_1
BF154347.1
ACC10410_1
HBC17831_1
FC815757.1
LLC00026_1
FK802965.1
FK800059.1
AW682850.1
FK802952.1
EL889800.1
JI464208.1
AS10169
AW755255.1
FF678883.1
JO469097.1
FK808519.1
FK803153.1
GE639126.1
SR01001
CGC00627_1
FK802688.1
CRC07461_1
FK809813.1
AYC04367_1
FC815009.1
FF679121.1
AS10318
CK850396.1
DA04388
AI444867.1
SRC00350_1
ASC02443_1
PT00542
CK850507.1
AS01129
FK804028.1
GE638718.1
FK803367.1
FK801903.1
CK850194.1
CK850525.1
FK802903.1
FK809579.1
FK801172.1
PPC01052_1
Dviv_isotig22436
GO239796.1
GO240501.1
AF285862.1
GO240127.1
GE639006.1
ASC00526_1
TDC02603_1
SRC00545_1
BM00550
BXC06244_1
PSC00716_2
Oden_isotig13911
AJ306290.1
ES743931.1
AA614882.1
FK802424.1
MC03610
GE638943.1
Oden_isotig13909
PT01294
CBC01328_1
MIC01297_1
FK807651.1
MI03206
JI463067.1
FC809602.1
ES413568.1
CJC06342_1
HCC07517_1
TDC02520_1
BE720947.1
SSC05673_1
JI219415.1
FK800886.1
Tcir_isotig29271
TS01157
FF682114.1
BMC05697_1
FK809409.1
BMC17479_1
JI170526.1
MHC01272_1
CR02142
CBC07047_1
MIC02948_1
PPC11668_1
XIC05237_1
Oden_isotig25532
AM743395.1
FK803955.1
FK808654.1
CK850579.1
Name_isotig08017
JI164083.1
EX500774.1
GO240434.1
FG588741.1
BMC00967_1
BM00094
Acan_isotig17077
Oden_isotig22472
HBC00743_1
SRC00620_1
AS10237
FF681879.1
FC817242.1
CJC00163_1
BE239177.1
FK809070.1
JI164158.1
JI164070.1
GW409454.1
FC815406.1
TX01584
WBC00936_1
FK808943.1
TCC00759_1
EX562479.1
BMC05557_1
FD517291.1
SS02276
CSC01171_1
GE638410.1
OVC09757_1
OVC01434_1
EX562007.1
BM174471.1
HGC01358_1
FC810432.1
FC810361.1
M74066.1
CB013433.1
TX01151
CRC01235_1
FC549000.1
SS00286
PT01504
FK803904.1
ASC00695_1
Name_isotig05674
FK808900.1
WBC00466_1
GO240017.1
FC816852.1
PPC00062_1
FK803615.1
OFC01265_1
PP01091
SS00331
FC810037.1
OFC01032_1
SS01504
GE638182.1
SR01540
JI168485.1
AI444888.1
OVC00584_1
CD374543.1
Dviv_isotig12023
FC548944.1
AS10535
SRC00638_1
FK799932.1
JO468111.1
DIC00460_1
JO469312.1
CK850714.1
FK800838.1
FK800573.1
CRC09156_1
EX501725.1
GO239410.1
PT02306
GW413414.1
GW714084.1
FK804282.1
HGC01071_1
AS00858
PP00570
FK801307.1
FK802252.1
TX00627
HC05681
BE238887.1
GE639342.1
FK803947.1
FK803228.1
FK809631.1
ALC01112_1
SS01266
FC815839.1
BMC07481_1
CK854723.1
PVC00588_1
BM00854
FK801350.1
AW682828.1
BE346041.1
FK805089.1
OVC00458_1
EF413918.1
AS03650
OFC00838_1
CK850254.1
SSC05741_1
GW411808.1
HG01183
BG360402.1
BMC11979_1
JO471421.1
GO240453.1
CK850503.1
SC00426
MI04341
CK855035.1
AM743336.1
BE239264.1
PTC00496_1
CK855384.1
WBC01458_1
AA294224.1
AS03889
FK802273.1
CK726210.1
MI03423
CK850587.1
JI177947.1
FK809888.1
AS10275
JI239323.1
FK805160.1
JI166543.1
ASC26237_1
DI00651
HG08592
ACC32497_1
HC00434
CK850660.1
MH05877
EL740219.1
Dviv_isotig34641
BMC01818_1
AS10231
FK808067.1
JI165145.1
OF01389
TX00342
SSC01004_1
OF01565
FF678167.1
AS03804
ASC04494_1
TCC01553_1
JO470194.1
GW714085.1
PT03030
AS10547
FK800073.1
CR08093
HBC04132_1
AF285857.1
MC03213
FG981100.1
FK808102.1
GE639480.1
AS10125
FK799864.1
ASC01109_1
AM743523.1
CK850691.1
Hbac_isotig01056
BU585796.1
AS03854
CK855040.1
Dviv_isotig12022
CK726257.1
FK801080.1
TLC00087_1
AW980220.1
CD455363.1
Acan_isotig08714
BE720854.1
EY460217.1
PTC01719_1
CRC06691_1
Dviv_isotig25139
AS09216
EX562853.1
JI174849.1
SR01635
MI00081
OF01566
FK802178.1
FK809088.1
HG01154
FK809432.1
XI04659
JI476535.1
JI166656.1
GE639009.1
AW980250.1
SS01320
GW714083.1
FK808580.1
Acan_isotig20126
FC814910.1
Tcol_isotig13978
FC816221.1
CGC01488_1
PVC02061_1
FC810776.1
EX560406.1
WBC00112_1
JI464393.1
AY033438.1
SRC07433_1
GE638117.1
HBC07402_1
BXC02747_1
TCC01675_1
SS00275
BMC08022_1
ASC02413_1
BE636486.1
FK802160.1
FK801377.1
GE639449.1
FG973998.1
R47746.1
FC817625.1
FK800834.1
FK800698.1
FK801269.1
AA680559.1
SSC02665_1
BMC11815_1
FK808838.1
Oden_isotig13910
Dviv_isotig22437
CBC04770_1
FK801961.1
WBC02640_1
TCC00643_1
FK806882.1
MCC05052_1
ASC00882_1
CK855346.1
FG353872.1
FK810036.1
PTC00715_1
BMC11521_1
CK850717.1
ACC00594_1
FF678583.1
SSC05834_1
JO473402.1
EE724181.1
Acan_isotig22146
CK855002.1
SS00586
BMC01437_1
CK854771.1
FK808403.1
TX00149
Associated_feature (32)
Experimental_infoRNAi_result (12)
Expr_pattern (15)
Drives_construct (151)
Construct_productWBCnstr00011688
WBCnstr00011704
WBCnstr00013869
WBCnstr00015881
WBCnstr00018819
WBCnstr00034149
Antibody (11)
Microarray_results (22)
Expression_cluster (308)
Interaction (231)
WBProcessWBbiopr:00000040
Map_infoMapIPosition27.9607Error0.002243
Well_ordered
PositiveInside_rearreDf3
eDf10
dxDf2
Positive_cloneF11C3Inferred_automaticallyFrom sequence, transcript, pseudogene data
SG25/36
Mapping_data2_point (22)
Multi_point (47)
Pos_neg_data (20)
Landmark_gene
Reference (599)
Remarkunc-54 posneg pcr data gives map conflict, spans deletion breakpoint ? jah 8.97
MethodGene