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WormBase Tree Display for Gene: WBGene00004886

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Name Class

WBGene00004886SMapS_parentSequenceY39A3CR
IdentityVersion1
NameCGC_namesmi-1Person_evidenceWBPerson1430
Sequence_nameY39A3CR.1
Molecular_name (12)
Other_nameCELE_Y39A3CR.1Accession_evidenceNDBBX284603
Public_namesmi-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:36WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsmi
Allele (94)
RNASeq_FPKM (74)
GO_annotation (17)
Contained_in_operonCEOP3072
Ortholog (31)
Structured_descriptionConcise_descriptionsmi-1 encodes the C. elegans ortholog of human Gemin2, a novel protein that interacts with the product of the survival motor neuron (SMN) gene, mutations in which are associated with spinal muscular atrophy; in C. elegans, smi-1 is an essential gene required for embryonic development past the mid-proliferation stage; in vitro, SMI-1 physically interacts with C. elegans SMN-1, indicating that the interaction between these two proteins is conserved; SMI-1 is expressed throughout development in multiple tissue types including the gut, neurons, and body wall muscles; SMI-1 localizes primarily to nuclei, with some protein also detected in the cytoplasm and in some neuronal processes.Paper_evidenceWBPaper00028478
Curator_confirmedWBPerson1843
Date_last_updated13 Feb 2007 00:00:00
Automated_descriptionInvolved in embryo development. Located in cytoplasm. Expressed in body wall musculature; intestine; and ventral cord neurons. Used to study spinal muscular atrophy. Is an ortholog of human GEMIN2 (gem nuclear organelle associated protein 2).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:12377Homo sapiensPaper_evidenceWBPaper00028478
Accession_evidenceOMIM253300
253400
253550
271150
Curator_confirmedWBPerson324
Date_last_updated28 Oct 2013 00:00:00
Disease_relevanceMutations in the human genes SMN1 and SMN2, which encode a RNA-binding protein, SMN, cause the inherited neuromuscular disorder, spinal muscular atrophy; this affects the control of muscle movement due to a loss of motor neurons in the spinal cord and the brainstem, leading to weakness and wasting (atrophy) of muscles; deletion of C. elegans smn-1/SMN, leads to several muscular defects (locomotive and pharyngeal pumping), and reduced lifespan; C. elegans has shown to be an effective genetic model to study SMN loss of functions defects; in mammals, SMN is tightly associated with SIP1/Gemin2; in C. elegans, the SMN and SIP orthologs, SMN-1 and SMI-1, interact and SMI-1 expression pattern and RNA interference phenotype show considerable overlap with those of smn-1; further, a yeast two-hybrid screen has identified several elegans smn-1 interacting proteins: F08F8.9c, K05C4.5, K07F5.1 (sequence similarity to proteins involved in RNA processing), F56D12.5a, RAN-2, ZK1320.7 (contain domains involved in RNA processing/metabolism, such as RNA-binding domains) and LET-418, MOG-4 (DEAD box helicase domains).Homo sapiensPaper_evidenceWBPaper00028478
Accession_evidenceOMIM253300
253550
253400
271150
600354
Curator_confirmedWBPerson324
Date_last_updated28 Oct 2013 00:00:00
Models_disease_in_annotationWBDOannot00000243
Molecular_infoCorresponding_CDSY39A3CR.1a
Y39A3CR.1b
Y39A3CR.1c
Y39A3CR.1d
Corresponding_CDS_historyY39A3CR.1:wp91
Y39A3CR.1b:wp278
Corresponding_transcriptY39A3CR.1a.1
Y39A3CR.1b.1
Y39A3CR.1c.1
Y39A3CR.1d.1
Other_sequenceMHC03264_1
CBC04805_1
MH01708
Associated_featureWBsf991410
WBsf1014321
WBsf224477
Experimental_infoRNAi_resultWBRNAi00103032Inferred_automaticallyRNAi_primary
WBRNAi00103033Inferred_automaticallyRNAi_primary
WBRNAi00020360Inferred_automaticallyRNAi_primary
Expr_patternExpr4282
Expr1027897
Expr1032425
Expr1159661
Expr2015918
Expr2034151
Drives_constructWBCnstr00011881
Construct_productWBCnstr00011881
Microarray_results (23)
Expression_clusterWBPaper00031040:TGF-beta_adult_downregulated
WBPaper00037950:germline-precursors_embryo_enriched
WBPaper00037950:PVD-OLL-neurons_L3-L4-larva_expressed
WBPaper00044656:tatn-1(qd182)_downregulated
WBPaper00044736:flat_dev_expression
WBPaper00045521:Gender_Neutral
WBPaper00045729:gld-4(RNAi)_downregulated
WBPaper00048923:Aging_regulated
WBPaper00048988:neuron_expressed
WBPaper00050488:adult_vs_dauer_regulated_N2_20C
WBPaper00050726:OsmoticStress_regulated_Food
WBPaper00050726:OsmoticStress_regulated_NoFood
WBPaper00050859:downregulated_P-granule(-)GFP(+)_vs_control_day2-adult
WBPaper00050990:body-muscle_expressed
WBPaper00050990:intestine_expressed
WBPaper00051039:germline_enriched
WBPaper00052884:emb-4(hc60)_downregulated
WBPaper00053302:zidovudine_72h_regulated
WBPaper00053321:PGCs_enriched_NuGen
WBPaper00053388:dauer_regulated_Cluster2
WBPaper00053599:oocyte_vs_mitosis_upregulated
WBPaper00055354:Rifampicin-Allantoin_upregulated
WBPaper00055648:germline_expressed
WBPaper00055971:nhl-2(ok818)_25C_upregulated
WBPaper00056090:E.faecalis_downregulated_hpx-2(dg047)
WBPaper00056139:soil-microbiota_downregulated
WBPaper00056826:SGP_biased
WBPaper00057288:iff-1(RNAi)_downregulated_transcript
WBPaper00058598:sin-3(tm1276)_upregulated
WBPaper00058691:sin-3(tm1276)_downregulated
WBPaper00060459:bcat-1(RNAi)_downregulated
WBPaper00061007:HB101_downregulated
WBPaper00061007:S.aquatilis_downregulated
WBPaper00061203:let-418(n3536)_downregulated
WBPaper00061203:sin-3(tm1276)_downregulated
WBPaper00061340:PVR
WBPaper00061341:28C_24h_downregulated
WBPaper00061527:F43G9.13-F33D11.12
WBPaper00062159:hda-2(ok1479)_downregulated
WBPaper00062325:muscle_enriched_coding-RNA
WBPaper00064005:starvation_upregulated_N2_mRNA
WBPaper00064716:paraquat_upregulated
WBPaper00065373:sek-1(km4)_upregulated_Ref
WBPaper00065993:glp-1(e2141)_downregulated
WBPaper00066146:germline-inx-14(RNAi)_downregulated_PA14
cgc4489_group_2
WBPaper00025032:cluster_72
WBPaper00025141:unc-4::GFP_Expressed_Genes
WBPaper00027111:rde-3(r459)_upregulated
WBPaper00036286:Pattern_H
WBPaper00040603:tdp-1(lf)_up_vs_N2_FC_1.2
WBPaper00041606:CE_X.nematophila_regulated
WBPaper00045960:L1-L4-lethargus_downregulated
WBPaper00045960:L4-lethargus_downregulated
[cgc5767]:expression_class_M
[cgc5767]:expression_class_SM
Interaction (23)
Map_infoMapIIIPosition-15.8236Error0.017184
PositivePositive_cloneY39A3CRInferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00028478
WBPaper00038491
WBPaper00055090
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