Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Gene: WBGene00004915

expand all nodes | collapse all nodes | view schema

Name Class

WBGene00004915EvidencePaper_evidenceWBPaper00005457
SMapS_parentSequenceW08E3
IdentityVersion1
NameCGC_namesnr-2Person_evidenceWBPerson167
Sequence_nameW08E3.1
Molecular_nameW08E3.1
W08E3.1.1
CE14704
Other_nameCELE_W08E3.1Accession_evidenceNDBBX284601
Public_namesnr-2
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:36WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsnr
Allele (23)
StrainWBStrain00035702
RNASeq_FPKM (74)
GO_annotation (19)
Contained_in_operonCEOP1692
Ortholog (41)
ParalogWBGene00021682Caenorhabditis elegansFrom_analysisPanther
Structured_descriptionAutomated_descriptionPredicted to enable RNA binding activity. Predicted to be involved in mRNA splicing, via spliceosome. Predicted to be located in cytoplasm. Predicted to be part of spliceosomal complex and spliceosomal snRNP complex. Expressed in gonad. Human ortholog(s) of this gene implicated in several diseases, including Prader-Willi syndrome; cerebrocostomandibular syndrome; and mixed connective tissue disease. Is an ortholog of human SNRPN (small nuclear ribonucleoprotein polypeptide N) and SNURF (SNRPN upstream open reading frame).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:3910Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11153)
DOID:11983Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11164)
DOID:0111248Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11153)
DOID:3492Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11153)
Molecular_infoCorresponding_CDSW08E3.1
Corresponding_transcriptW08E3.1.1
Other_sequence (84)
Associated_featureWBsf643797
WBsf218713
WBsf218714
WBsf218715
Experimental_infoRNAi_result (26)
Expr_patternExpr2229
Expr1016560
Expr1032444
Expr1158523
Expr2015966
Expr2034201
Drives_constructWBCnstr00035325
WBCnstr00043011
Construct_productWBCnstr00035325
WBCnstr00043011
AntibodyWBAntibody00000549
WBAntibody00000550
WBAntibody00000551
WBAntibody00000552
WBAntibody00000553
Microarray_results (21)
Expression_cluster (168)
Interaction (259)
Map_infoMapIPosition18.3808Error0.326492
PositivePositive_cloneW08E3Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4680
5003
Pseudo_map_position
Reference (12)
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