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WormBase Tree Display for Gene: WBGene00004699

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Name Class

WBGene00004699SMapS_parentSequenceW02B12
IdentityVersion1
NameCGC_namersp-2Person_evidenceWBPerson297
Sequence_nameW02B12.2
Molecular_nameW02B12.2
W02B12.2.1
CE03762
Other_namesrp-4
CeSRp40
CELE_W02B12.2Accession_evidenceNDBBX284602
Public_namersp-2
DB_infoDatabaseAceViewgene2L742
WormQTLgeneWBGene00004699
WormFluxgeneWBGene00004699
NDBlocus_tagCELE_W02B12.2
PanthergeneCAEEL|WormBase=WBGene00004699|UniProtKB=Q23120
familyPTHR23147
NCBIgene174747
RefSeqproteinNM_064040.7
SwissProtUniProtAccQ23120
TREEFAMTREEFAM_IDTF351335
UniProt_GCRPUniProtAccQ23120
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:36WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classrsp
Allele (30)
StrainWBStrain00035790
RNASeq_FPKM (74)
GO_annotation (23)
Ortholog (31)
ParalogWBGene00004698Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00004700Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00004702Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00013307Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00020399Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionrsp-2 encodes the C. elegans ortholog of the vertebrate SRp40 splicing factor and member of the SR protein family of nuclear phosphoproteins that are required for constitutive splicing and influence alternative splicing regulation.Paper_evidenceWBPaper00003988
Curator_confirmedWBPerson1843
Date_last_updated20 Mar 2012 00:00:00
Automated_descriptionPredicted to enable RNA binding activity. Involved in developmental process involved in reproduction; nematode larval development; and regulation of growth rate. Located in nucleus. Expressed widely. Human ortholog(s) of this gene implicated in several diseases, including Huntington's disease; carcinoma (multiple); and proliferative diabetic retinopathy. Is an ortholog of human SRSF5 (serine and arginine rich splicing factor 5) and SRSF6 (serine and arginine rich splicing factor 6).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:4467Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10787,HGNC:10788)
DOID:234Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10787,HGNC:10788)
DOID:0070168Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10788)
DOID:4159Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10788)
DOID:1324Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10788)
DOID:12858Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10788)
DOID:13207Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10788)
DOID:1612Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10787)
Molecular_infoCorresponding_CDSW02B12.2
Corresponding_transcriptW02B12.2.1
Other_sequence (61)
Associated_featureWBsf650575
WBsf650576
WBsf650577
WBsf655392
WBsf665274
WBsf666138
WBsf989763
WBsf1013240
WBsf223935
WBsf223936
Experimental_infoRNAi_result (35)
Expr_patternExpr1142
Expr1013873
Expr1032319
Expr1158104
Expr2015559
Expr2033794
Drives_constructWBCnstr00010104
Microarray_results (20)
Expression_cluster (138)
Interaction (28)
Map_infoMapIIPosition3.46842Error0.000911
PositivePositive_cloneW02B12Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4647
Pseudo_map_position
Reference (11)
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