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WormBase Tree Display for Gene: WBGene00006820

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Name Class

WBGene00006820SMapS_parentSequenceCHROMOSOME_I
IdentityVersion2
NameCGC_nameunc-89Person_evidenceWBPerson261
Sequence_nameC09D1.1
Molecular_nameC09D1.1a
C09D1.1a.1
CE30426
C09D1.1b
CE34251
C09D1.1c
CE34252
C09D1.1d
CE37701
C09D1.1e
CE37702
C09D1.1f
CE37703
C09D1.1g
CE52389
C09D1.1h
CE52068
C09D1.1i
CE52386
C09D1.1j
CE52284
C09D1.1k
CE52154
C09D1.1l
CE52202
C09D1.1m
CE52124
C09D1.1n
CE52393
C09D1.1o
CE52289
C09D1.1p
CE52385
C09D1.1b.1
C09D1.1c.1
C09D1.1d.1
C09D1.1e.1
C09D1.1f.1
C09D1.1g.1
C09D1.1h.1
C09D1.1i.1
C09D1.1j.1
C09D1.1k.1
C09D1.1l.1
C09D1.1m.1
C09D1.1n.1
C09D1.1o.1
C09D1.1p.1
Other_namephm-1
CELE_C09D1.1Accession_evidenceNDBBX284601
Public_nameunc-89
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:43WBPerson1971EventImportedInitial conversion from geneace
221 Dec 2004 16:19:44WBPerson2970EventAcquires_mergeWBGene00043148
Acquires_mergeWBGene00043148
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classunc
Reference_alleleWBVar00144017
Allele (812)
Legacy_informatione1460 : good movement slightly small thin and transparent; abnormal reduced birefringence in body wall and pharyngeal muscle; thick filaments disarranged no M-line. ES1 ME3. NA > 10 (st85amber r291 etc.).
[Leon Avery] Pharyngeal contractions are feeble. Worms are small and starved.
See also ad539, e1460, e2338
[C.elegansII] e1460 : good movement, slightly small, thin and transparent; abnormal reduced birefringence in body wall and pharyngeal muscle; thick filaments disarranged, no M-line. ES1 ME3. OA>10: st85amb, r291,ad539 (pka phm-1, worms small and starved, feeble pharyngeal contractions), e2338amb,st515::Tc1 etc. Cloned: encodes 750 kD protein related to UNC-22 (twitchin). Antibodies stain middle of A bands. [Waterston et al. 1980; GB]
StrainWBStrain00002024
WBStrain00002131
WBStrain00031887
WBStrain00033489
WBStrain00036403
WBStrain00036411
WBStrain00004337
RNASeq_FPKM (74)
GO_annotation (49)
Ortholog (56)
ParalogWBGene00001000Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001863Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00004130Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00006436Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00006759Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00011880Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00017657Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00019727Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionunc-89 encodes several protein isoforms variably characterized by the presence or absence of SH3, DH, PH, immunoglobulin and myosin light chain kinase (MLCK)-like protein kinase domains; during development, unc-89 is required for proper organization of A bands in striated muscle and thus for fully normal locomotion, pharyngeal muscle contractions, and body size; unc-89 is expressed in body wall muscle, pharyngeal muscle and some cells in the tail; UNC-89 protein isoforms localize to the middle of A-bands, consistent with UNC-89 being an M line component; UNC-89 interacts with the SCPL-1 phosphatase both in vitro and in vivo.Paper_evidenceWBPaper00002411
WBPaper00024436
WBPaper00031595
Curator_confirmedWBPerson1843
Date_last_updated16 Dec 2011 00:00:00
Automated_descriptionEnables MATH domain binding activity; enzyme binding activity; and guanyl-nucleotide exchange factor activity. Involved in several processes, including myofibril assembly; pharyngeal gland morphogenesis; and regulation of striated muscle contraction. Located in M band. Expressed in alimentary muscle; gonad; tail; and vulval muscle. Human ortholog(s) of this gene implicated in centronuclear myopathy 5. Is an ortholog of human SPEG (striated muscle enriched protein kinase).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_modelDOID:0111222Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:16901)
Molecular_infoCorresponding_CDS (16)
Corresponding_CDS_historyC09D1.1g:wp261
Corresponding_transcript (16)
Other_sequence (139)
Associated_feature (48)
Experimental_infoRNAi_result (25)
Expr_pattern (15)
Drives_constructWBCnstr00002806
WBCnstr00002896
WBCnstr00011122
Construct_productWBCnstr00011122
WBCnstr00022809
WBCnstr00022810
AntibodyWBAntibody00000105
WBAntibody00000106
WBAntibody00000758
WBAntibody00000759
Microarray_results (68)
Expression_cluster (231)
Interaction (87)
WBProcessWBbiopr:00000006
Map_infoMapIPosition-1.73264Error0.009136
Well_ordered
PositiveInside_rearrsDf4
Positive_cloneC09D1Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point (15)
Pos_neg_data506
6165
6270
6339
4746
3932
3933
4559
5704
Reference (90)
MethodGene