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WormBase Tree Display for Gene: WBGene00004919

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Name Class

WBGene00004919EvidencePaper_evidenceWBPaper00005457
SMapS_parentSequenceY49E10
IdentityVersion1
NameCGC_namesnr-6Person_evidenceWBPerson167
Sequence_nameY49E10.15
Molecular_nameY49E10.15
Y49E10.15.1
CE22230
Other_nameCELE_Y49E10.15Accession_evidenceNDBBX284603
Public_namesnr-6
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:36WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsnr
Allele (16)
StrainWBStrain00051373
RNASeq_FPKM (74)
GO_annotation (22)
Ortholog (34)
Structured_descriptionConcise_descriptionsnr-6 encodes the C. elegans ortholog of the small nuclear ribonucleoprotein E, one of seven subunits of the heptameric Sm complex required for the biogenesis and function of snRNPs that catalyze mRNA splicing; in addition to its predicted role in pre-mRNA processing, SNR-6 activity is essential for embryogenesis and is required for several aspects of germ cell specification including cell division patterns, localization and subcellular distribution of P granules, maintenance of transcriptional quiescence, and expression of the germ lineage-specific proteins PIE-1, GLD-1, and NOS-2; snr-6 is also required for wild-type levels of fertility; immunostaining of adults and embryos using antibodies raised against mammalian Sm proteins suggests that SNR-6 localizes to the nucleus and cytoplasm in many cell types, as well as to P granules in germ cells and their embryonic precursors.Paper_evidenceWBPaper00004403
WBPaper00005457
WBPaper00006395
WBPaper00025054
WBPaper00027038
Curator_confirmedWBPerson1843
Date_last_updated25 Jul 2006 00:00:00
Automated_descriptionPredicted to enable RNA binding activity. Predicted to be involved in spliceosomal snRNP assembly. Located in P granule. Expressed in gonad. Human ortholog(s) of this gene implicated in several diseases, including carcinoma (multiple); hypotrichosis (multiple); and lupus nephritis. Is an ortholog of human SNRPE (small nuclear ribonucleoprotein polypeptide E).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:0110698Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11161)
DOID:0110708Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11161)
DOID:769Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11161)
DOID:0080162Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11161)
DOID:9261Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11161)
DOID:9952Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11161)
DOID:3910Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11161)
DOID:10283Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11161)
DOID:684Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11161)
Molecular_infoCorresponding_CDSY49E10.15
Corresponding_transcriptY49E10.15.1
Other_sequence (82)
Associated_featureWBsf667524
WBsf667525
WBsf227665
Experimental_infoRNAi_result (31)
Expr_patternExpr2229
Expr1024336
Expr1032448
Expr1160453
Expr2015970
Expr2034205
AntibodyWBAntibody00000550
WBAntibody00000552
WBAntibody00000553
Microarray_results (18)
Expression_cluster (149)
Interaction (203)
Map_infoMapIIIPosition17.7919Error0.019258
PositivePositive_cloneY49E10Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00005457
WBPaper00027038
WBPaper00038491
WBPaper00040897
WBPaper00045396
WBPaper00046572
WBPaper00049828
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