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WormBase Tree Display for Gene: WBGene00004706

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Name Class

WBGene00004706SMapS_parentSequenceF28D9
IdentityVersion1
NameCGC_namersr-1Person_evidenceWBPerson297
Sequence_nameF28D9.1
Molecular_nameF28D9.1
F28D9.1.1
CE30346
Other_nameCeSRm160
CELE_F28D9.1Accession_evidenceNDBBX284601
Public_namersr-1
DB_infoDatabaseAceViewgene1L770
WormQTLgeneWBGene00004706
WormFluxgeneWBGene00004706
NDBlocus_tagCELE_F28D9.1
PanthergeneCAEEL|WormBase=WBGene00004706|UniProtKB=O62185
familyPTHR23148
NCBIgene173013
RefSeqproteinNM_001383730.2
TREEFAMTREEFAM_IDTF318972
TrEMBLUniProtAccO62185
UniProt_GCRPUniProtAccO62185
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:36WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classrsr
Allele (66)
StrainWBStrain00032156
RNASeq_FPKM (74)
GO_annotation00037254
00037255
00037256
00037257
Contained_in_operonCEOP1896
Ortholog (18)
Structured_descriptionConcise_descriptionrsr-1 encodes the C. elegans homolog of the SRm160 (serine/arginine-repeat related nuclear matrix protein of 160kDa) splicing coactivator; rsr-1 is an essential gene that is required for development, including normal pharyngeal morphology.Paper_evidenceWBPaper00005023
WBPaper00040399
WBPaper00026804
Curator_confirmedWBPerson1843
Date_last_updated16 Nov 2011 00:00:00
Automated_descriptionPredicted to be involved in regulation of mRNA splicing, via spliceosome. Predicted to be located in nucleus. Predicted to be part of spliceosomal complex. Expressed in hypodermis. Human ortholog(s) of this gene implicated in gestational diabetes. Is an ortholog of human SRRM1 (serine and arginine repetitive matrix 1).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:11714Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:16638)
Molecular_infoCorresponding_CDSF28D9.1
Corresponding_CDS_historyF28D9.1:wp74
Corresponding_transcriptF28D9.1.1
Other_sequence (35)
Associated_featureWBsf220313
WBsf220314
WBsf220315
Experimental_infoRNAi_result (26)
Expr_patternExpr149
Expr1016657
Expr1032326
Expr1149742
Expr2015566
Expr2033801
Microarray_results (17)
Expression_cluster (87)
Interaction (43)
Map_infoMapIPosition7.24727Error0.098402
PositivePositive_cloneF28D9Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4851
4818
4410
5393
Pseudo_map_position
ReferenceWBPaper00003988
WBPaper00005960
WBPaper00006292
WBPaper00026804
WBPaper00032289
WBPaper00038491
WBPaper00040399
WBPaper00055090
WBPaper00064339
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