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WormBase Tree Display for Gene: WBGene00004916

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Name Class

WBGene00004916EvidencePaper_evidenceWBPaper00005457
SMapS_parentSequenceT28D9
IdentityVersion1
NameCGC_namesnr-3Person_evidenceWBPerson167
Sequence_nameT28D9.10
Molecular_nameT28D9.10a
T28D9.10a.1
CE02065
T28D9.10b
CE51626
T28D9.10b.1
Other_nameCELE_T28D9.10Accession_evidenceNDBBX284602
Public_namesnr-3
DB_infoDatabaseAceViewgene2G778
WormQTLgeneWBGene00004916
WormFluxgeneWBGene00004916
NDBlocus_tagCELE_T28D9.10
PanthergeneCAEEL|WormBase=WBGene00004916|UniProtKB=Q10013
familyPTHR23338
NCBIgene174072
RefSeqproteinNM_062905.8
NM_001330951.3
SwissProtUniProtAccQ10013
TrEMBLUniProtAccM1ZJ32
UniProt_GCRPUniProtAccQ10013
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:36WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsnr
Allele (13)
StrainWBStrain00037033
RNASeq_FPKM (74)
GO_annotation (25)
Ortholog (35)
ParalogWBGene00003078Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00004914Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00044916Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionsnr-3 encodes an ortholog of human small nuclear ribonucleoprotein Sm D1, a protein that forms part of a heptameric complex required for biogenesis and function of the snRNPs that catalyze mRNA splicing; in combination with the gene that encodes the human Sm D2 ortholog (snr-4), snr-3 affects embryonic viability and nuclear association and localization of P granules in embryos, based on an RNAi assay; affects embryonic and larval viability based on large-scale RNAi assays; snr-3 is expressed in embryos and adult gonads.Paper_evidenceWBPaper00005457
Curator_confirmedWBPerson48
Date_last_updated11 Jul 2005 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 nasopharynx carcinoma; nephritis; and systemic lupus erythematosus. Is an ortholog of human SNRPD1 (small nuclear ribonucleoprotein D1 polypeptide).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:9261Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11158)
DOID:9074Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11158)
DOID:576Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11158)
DOID:65Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11158)
DOID:10952Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11158)
Molecular_infoCorresponding_CDST28D9.10a
T28D9.10b
Corresponding_CDS_historyT28D9.10b:wp253
Corresponding_transcriptT28D9.10a.1
T28D9.10b.1
Other_sequence (51)
Associated_featureWBsf650149
WBsf223183
WBsf223184
Experimental_infoRNAi_result (23)
Expr_patternExpr2229
Expr1020664
Expr1032445
Expr1157958
Expr2015967
Expr2034202
Drives_constructWBCnstr00035324
Construct_productWBCnstr00035324
AntibodyWBAntibody00000549
WBAntibody00000550
WBAntibody00000551
WBAntibody00000552
WBAntibody00000553
Microarray_results (22)
Expression_cluster (178)
Interaction (204)
Map_infoMapIIPosition-0.218968Error0.002781
PositivePositive_cloneT28D9Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00005457
WBPaper00027057
WBPaper00038491
WBPaper00046572
WBPaper00049828
WBPaper00055090
WBPaper00063976
WBPaper00064663
RemarkLocus was previously incorrectly associated with C52E4.3. [krb 030219]
Map 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