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WormBase Tree Display for Gene: WBGene00004887

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Name Class

WBGene00004887SMapS_parentSequenceC41G7
IdentityVersion1
NameCGC_namesmn-1Person_evidenceWBPerson651
Sequence_nameC41G7.1
Molecular_nameC41G7.1a
C41G7.1a.1
CE08665
C41G7.1b
CE27843
C41G7.1a.2
C41G7.1b.1
Other_nameSMNAccession_evidenceEMBLAF156887
CELE_C41G7.1Accession_evidenceNDBBX284601
Public_namesmn-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:36WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsmn
Allele (16)
StrainWBStrain00024206
WBStrain00024207
WBStrain00008302
WBStrain00047286
Component_of_genotype (15)
RNASeq_FPKM (74)
GO_annotation (13)
Ortholog (32)
ParalogWBGene00004891Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionsmn-1 encodes a homolog of human SMN, which when mutated leads to spinal muscular atrophy (OMIM:253300).Paper_evidenceWBPaper00004103
Curator_confirmedWBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionEnables protein self-association. Involved in several processes, including determination of adult lifespan; pharyngeal pumping; and vulval development. Located in nucleus. Expressed in several structures, including body wall musculature; excretory cell; hypodermis; intestine; and vulval muscle. Used to study spinal muscular atrophy. Human ortholog(s) of this gene implicated in spinal muscular atrophy (multiple). Is an ortholog of human SMN1 (survival of motor neuron 1, telomeric) and SMN2 (survival of motor neuron 2, centromeric).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_info (3)
Models_disease_asserted (17)
Molecular_infoCorresponding_CDSC41G7.1a
C41G7.1b
Corresponding_transcriptC41G7.1a.1
C41G7.1a.2
C41G7.1b.1
Other_sequence (49)
Associated_featureWBsf649480
WBsf220093
WBsf220094
Experimental_infoRNAi_result (22)
Expr_patternExpr1229
Expr1230
Expr1231
Expr12328
Expr13407
Expr1018011
Expr1032426
Expr1146303
Expr2015920
Expr2034153
Drives_constructWBCnstr00010166
WBCnstr00023121
WBCnstr00035340
Construct_productWBCnstr00010166
WBCnstr00020789
WBCnstr00022986
WBCnstr00023121
WBCnstr00035340
WBCnstr00039444
Regulate_expr_clusterWBPaper00056809:smn-1(ok355)_downregulated
WBPaper00056809:smn-1(ok355)_upregulated
Microarray_results (23)
Expression_cluster (109)
Interaction (93)
WBProcessWBbiopr:00000001
Map_infoMapIPosition3.78179Error0.001059
PositivePositive_cloneC41G7Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4667
4707
Pseudo_map_position
Reference (69)
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