Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Gene: WBGene00001131

expand all nodes | collapse all nodes | view schema

Name Class

WBGene00001131SMapS_parentSequenceCHROMOSOME_I
IdentityVersion1
NameCGC_namedys-1Person_evidenceWBPerson571
Sequence_nameF15D3.1
Molecular_name (30)
Other_nameCELE_F15D3.1Accession_evidenceNDBBX284601
Public_namedys-1
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:23WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classdys
Allele (647)
Possibly_affected_byWBVar02153522
StrainWBStrain00002611
WBStrain00024335
WBStrain00024340
WBStrain00024342
WBStrain00024343
WBStrain00037736
WBStrain00004037
WBStrain00048693
RNASeq_FPKM (74)
GO_annotation (37)
Ortholog (37)
Structured_descriptionConcise_descriptionThe dys-1 gene encodes an ortholog of human DMD, which when mutated leads to Duchenne muscular dystrophy (OMIM:310200).Paper_evidenceWBPaper00004103
WBPaper00005175
Curator_confirmedWBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable actin binding activity and zinc ion binding activity. Involved in several processes, including forward locomotion; muscle cell cellular homeostasis; and sarcomere organization. Located in striated muscle dense body. Part of dystrobrevin complex. Expressed in body wall musculature; head muscle; pharyngeal muscle cell; and vulval muscle. Used to study Duchenne muscular dystrophy. Human ortholog(s) of this gene implicated in several diseases, including Becker muscular dystrophy; Duchenne muscular dystrophy; cognitive disorder; dilated cardiomyopathy (multiple); and ovarian cancer. Is an ortholog of human DMD (dystrophin) and UTRN (utrophin).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:11723Homo sapiensPaper_evidenceWBPaper00003867
WBPaper00003395
WBPaper00044415
WBPaper00035094
Accession_evidenceOMIM300376
310200
Curator_confirmedWBPerson324
Date_last_updated22 May 2017 00:00:00
Potential_modelDOID:11723Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2928)
DOID:0081164Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2928)
DOID:1561Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2928)
DOID:2394Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12635)
DOID:0110461Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2928)
DOID:12930Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2928)
DOID:1059Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2928)
DOID:9883Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2928)
Disease_relevanceMutations in human dystrophin are associated with the Duchenne and Becker types of muscular dystrophy, that affect skeletal muscles used for movement, and heart (cardiac) muscle; in C. elegans, loss-of-function mutants in dys-1 (cx18,cx26,cx35,cx40), the ortholog of human dystrophin/utrophin, display locomotion defects like hyperactivity and hypercontraction, and are hypersensitive to acetylcholine and to the acetylcholinesterase inhibitor, aldicarb, suggesting that dys-1 plays a role in the muscle response to acetylcholine; a chimeric transgene in which the C-terminal end of the elegans DYS-1 protein is replaced by the human dystrophin sequence is able to partly suppress the phenotype of the dys-1 mutants; however, the genetic model for progressive myopathy in C. elegans consists of the dys-1 mutation combined with a mutation in hlh-1, the MyoD ortholog (dys-1(cx18);hlh-1(cc561ts), these animals display time-dependent muscle degeneration; use of this model has identified several genes, that play a role in muscle degeneration, eg., dyc-1/nitric oxide synthase (nNOS)-binding protein CAPON.Homo sapiensPaper_evidenceWBPaper00003867
Accession_evidenceOMIM300377
Curator_confirmedWBPerson324
Date_last_updated17 May 2017 00:00:00
Models_disease_asserted (21)
Molecular_infoCorresponding_CDSF15D3.1a
F15D3.1b
F15D3.1c
F15D3.1d
F15D3.1e
F15D3.1f
F15D3.1g
F15D3.1h
F15D3.1i
F15D3.1j
Corresponding_CDS_historyF15D3.1a:wp47
Corresponding_transcriptF15D3.1a.1
F15D3.1b.1
F15D3.1c.1
F15D3.1d.1
F15D3.1e.1
F15D3.1f.1
F15D3.1g.1
F15D3.1h.1
F15D3.1i.1
F15D3.1j.1
Other_sequence (44)
Associated_feature (19)
Experimental_infoRNAi_result (13)
Expr_pattern (12)
Drives_constructWBCnstr00003169
WBCnstr00010181
Construct_productWBCnstr00007078
WBCnstr00008412
WBCnstr00010181
WBCnstr00011497
Regulate_expr_clusterWBPaper00028474:dys-1_downregulated
WBPaper00028474:dys-1_upregulated
AntibodyWBAntibody00003001
Microarray_results (34)
Expression_clusterWBPaper00029359_1183
WBPaper00029359_1280
WBPaper00029359_1310
WBPaper00029359_1362
WBPaper00029359_1364
WBPaper00029359_1444
WBPaper00029359_1504
WBPaper00029359_1578
WBPaper00029359_1604
WBPaper00029359_1636
WBPaper00031040:TGF-beta_adult_upregulated
WBPaper00033065:clk-1(qm30)_upregulated
WBPaper00036375:enriched_in_PVD_OLL
WBPaper00037950:bodywall-muscle_CoreEnriched
WBPaper00037950:bodywall-muscle_embryo_enriched
WBPaper00037950:bodywall-muscle_embryo_SelectivelyEnriched
WBPaper00037950:bodywall-muscle_L1-larva_expressed
WBPaper00037950:bodywall-muscle_L2-larva_expressed
WBPaper00037950:bodywall-muscle_larva_enriched
WBPaper00037950:bodywall-muscle_larva_SelectivelyEnriched
WBPaper00037950:dopaminergic-neurons_L1-larva_expressed
WBPaper00037950:hypodermis_L1-larva_expressed
WBPaper00037950:hypodermis_L3-L4-larva_expressed
WBPaper00037950:PVD-OLL-neurons_L3-L4-larva_expressed
WBPaper00038438:D.coniospora_12hr_downregulated_RNAseq
WBPaper00038438:E.faecalis_24hr_upregulated_TilingArray
WBPaper00038438:Harposporium_24hr_downregulated_RNAseq
WBPaper00038438:S.marcescens_24hr_downregulated_TilingArray
WBPaper00042561:smgl-1(RNAi)_upregulated
WBPaper00044501:gld-1_let-7_regulated
WBPaper00044736:flat_dev_expression
WBPaper00044786:emr-1(RNAi);lem-2(tm1582)_upregulated
WBPaper00045420:fertilization_downregulated_transcript
WBPaper00045521:Gender_Neutral
WBPaper00046121:mesoderm_unique
WBPaper00046509:htz-1(ok3099)_downregulated
WBPaper00048923:Aging_regulated
WBPaper00048988:neuron_expressed
WBPaper00050053:muscle_enriched_Day4
WBPaper00050488:20C_vs_25C_regulated_N2_adult
WBPaper00050488:adult_vs_dauer_regulated_N2_20C
WBPaper00050859:upregulated_P-granule(-)GFP(+)_vs_control_day2-adult
WBPaper00050859:upregulated_P-granule(-)GFP(-)_vs_control_day2-adult
WBPaper00050990:arcade_intestinal-valve_expressed
WBPaper00050990:body-muscle_expressed
WBPaper00050990:GABAergic-neuron_expressed
WBPaper00050990:hypodermis_expressed
WBPaper00050990:NMDA-neuron_expressed
WBPaper00050990:pharynx_expressed
WBPaper00051245:body-wall-muscle_cytoplasm_expressed
WBPaper00053184:sma-2(rax5)_upregulated
WBPaper00053184:sma-4(rax3)_upregulated
WBPaper00053295:lin-22(icb38)_upregulated
WBPaper00053814:15C_downregulated_OP50
WBPaper00054493:hpl-2(tm1489)_upregulated
WBPaper00054758:alg-1(gk204)_upregulated
WBPaper00055226:ADR-2_target_N2
WBPaper00055334:DLC-1_interacting
WBPaper00055354:Rapamycin-Allantoin_downregulated
WBPaper00055354:Rapamycin-Psora-Allantoin_upregulated
WBPaper00055354:Rapamycin-Rifampicin-Allantoin_upregulated
WBPaper00055354:Rapamycin-Rifampicin-Psora_upregulated
WBPaper00055354:Rapamycin-Rifampicin_upregulated
WBPaper00055354:Rapamycin_downregulated
WBPaper00056139:gut-microbiota_downregulated
WBPaper00056139:soil-microbiota_downregulated
WBPaper00056275:P.aeruginosa_downregulated
WBPaper00056275:P.aeruginosa_downregulated_pmk-1(km25)_dependent
WBPaper00056443:sek-1(km4)_upregulated
WBPaper00056471:aak-1(tm1944);aak-2(ok524)_upregulated
WBPaper00056826:hmc_biased
WBPaper00057068:numr-1(RNAi)_downregulated
WBPaper00057154:HeatShock_upregulated_mRNA
WBPaper00057161:meg-3(tm4259)_meg-4(ax2026)_downregulated_endo-siRNA_targets
WBPaper00058598:sin-3(tm1276)_downregulated
WBPaper00058958:100mGy-irradiation-72h_upregulated
WBPaper00059027:neuron-synapses_enriched
WBPaper00059664:srbc-48(ac23)_upregulated
WBPaper00059987:Wounding_downregulated
WBPaper00060014:set-2(tm1630)_downregulated
WBPaper00060014:set-2(zr2012)_upregulated
WBPaper00060661:sensory-neuron_enriched
WBPaper00060683:hlh-11(ko1)_upregulated
WBPaper00060871:M.humicola-extract_1h_regulated
WBPaper00060911:prx-5(RNAi)_upregulated_mRNA
WBPaper00061203:sin-3(tm1276)_upregulated
WBPaper00061203:spr-1(ok2144)_upregulated
WBPaper00061285:wounding_24h_downregulated
WBPaper00061340:BWM_anterior
WBPaper00061340:DVC_parent
WBPaper00061340:mu_sph
WBPaper00061340:PVP
WBPaper00061340:PVQ_parent
WBPaper00061527:T16H12.9-kin-9_20752
WBPaper00061818:ELKS-1_interacting
WBPaper00061902:CAMT-1_interacting
WBPaper00062159:hda-2(ok1479)_upregulated
WBPaper00062193:skn-1(RNAi)_downregulated
WBPaper00062325:muscle_enriched_coding-RNA
WBPaper00063976:micu-1(bon20)_upregulated
WBPaper00064071:NHR-49_interacting
WBPaper00064088:Day-1-adult_vs_L4_downregulated_fem-3(q20)
WBPaper00064088:Day-3-adult_vs_L4_downregulated_fem-3(q20)
WBPaper00064088:Day-3-adult_vs_L4_downregulated_glp-1(e2141)
WBPaper00064306:Agaro-oligosaccharides_upregulated
WBPaper00064735:bet-1B(OE)mys-1(RNAi)_vs_mys-1(RNAi)_downregulated
WBPaper00064871:hypoxia_downregulated_F2
WBPaper00064992:heat-shock_upregulated
WBPaper00065086:JU1400_N.ferruginous_regulated
WBPaper00065373:Cisplatin_downregulated_WT
WBPaper00065373:sek-1(km4)_downregulated_Ref
WBPaper00065581:hpk-1(pk1393)_upregulated
WBPaper00065841:1_1
WBPaper00065841:4_0
cgc4386_cluster_5_2
cgc4489_group_13
cgc4489_group_20
WBPaper00025141:N2_Expressed_Genes
WBPaper00026929:Resveratrol_regulated_daf-16
WBPaper00026929:sir-2.1_overexpression_regulated
WBPaper00031003:0hr_muscle_enriched
WBPaper00031003:24hr_muscle_enriched
WBPaper00031003:hlh_1_enriched
WBPaper00031003:total_muscle_enriched
WBPaper00034661:AgNPs_downregulated
WBPaper00036123:Cadmium_regulated
WBPaper00040184:hcf-1down_sir-2.1nc_daf-2nc
WBPaper00040210:Chlorpyrifos_24C_regulated
WBPaper00040858:eQTL_age_regulated_developing
WBPaper00040858:eQTL_regulated_developing
WBPaper00040858:eQTL_regulated_juvenile
WBPaper00040963:Q100_down
WBPaper00040963:Q200_down
WBPaper00041606:CE_X.nematophila_regulated
WBPaper00041939:control_vs_UVC-EtBr-exposed_48h
WBPaper00041939:UVC-EtBr-exposed_vs_EtBr-exposed_3h
WBPaper00041939:UVC-EtBr-exposed_vs_UVC-exposed_48h
WBPaper00045673:colistin_upregulated
WBPaper00057098:SiO2-nanoparticles_upregulated
[cgc5767]:expression_class_M
[cgc5767]:expression_class_SM
[cgc6390]:Cluster_C
Interaction (61)
Map_infoMapIPosition9.11232
PositivePositive_cloneF15D3Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4272
5386
Pseudo_map_position
Reference (86)
RemarkSequence connection from [Segalat L]
Map 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
[210510 skd] Modified Map position as it was a reverse physical that could not be fixed by automated methods. (9.05343)
MethodGene