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WormBase Tree Display for Gene: WBGene00004187

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Name Class

WBGene00004187EvidencePerson_evidenceWBPerson395
WBPerson71
SMapS_parentSequenceC50C3
IdentityVersion1
NameCGC_nameprp-8
Sequence_nameC50C3.6
Molecular_nameC50C3.6
C50C3.6.1
CE00122
Other_nameCELE_C50C3.6Accession_evidenceNDBBX284603
Public_nameprp-8
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:34WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classprp
Allele (77)
StrainWBStrain00037786
WBStrain00055589
WBStrain00055587
WBStrain00055586
WBStrain00048023
WBStrain00055590
Component_of_genotypeWBGenotype00000120
RNASeq_FPKM (74)
GO_annotation (22)
Ortholog (40)
Structured_descriptionConcise_descriptionprp-8 is orthologous to the human gene SIMILAR TO U5 SNRNP-SPECIFIC PROTEIN (220 KD), ORTHOLOG OF S.Curator_confirmedWBPerson1823
WBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable pre-mRNA intronic binding activity and snRNA binding activity. Predicted to be involved in spliceosomal tri-snRNP complex assembly. Predicted to be located in nucleus. Predicted to be part of U5 snRNP and catalytic step 2 spliceosome. Expressed in germ line. Used to study retinitis pigmentosa 13. Human ortholog(s) of this gene implicated in retinitis pigmentosa 13. Is an ortholog of human PRPF8 (pre-mRNA processing factor 8).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_infoExperimental_modelDOID:10584Homo sapiensPaper_evidenceWBPaper00032287
Curator_confirmedWBPerson38202
Date_last_updated22 May 2018 00:00:00
DOID:0110403Homo sapiensPaper_evidenceWBPaper00059062
Curator_confirmedWBPerson324
Date_last_updated26 May 2022 00:00:00
Potential_modelDOID:0110403Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:17340)
DOID:10584Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:17340)
Models_disease_assertedWBDOannot00000523
WBDOannot00001205
WBDOannot00001206
WBDOannot00001209
WBDOannot00001210
WBDOannot00001211
WBDOannot00001212
Molecular_infoCorresponding_CDSC50C3.6
Corresponding_transcriptC50C3.6.1
Other_sequence (108)
Associated_feature (12)
Experimental_infoRNAi_result (17)
Expr_patternChronogram353
Expr5548
Expr12531
Expr12730
Expr1019555
Expr1032047
Expr1146854
Expr2015116
Expr2033354
Drives_constructWBCnstr00002926
WBCnstr00035647
Construct_productWBCnstr00035647
Regulate_expr_clusterWBPaper00042477:prp-8(RNAi)_downregulated_RNAseq
WBPaper00042477:prp-8(RNAi)_upregulated_RNAseq
Microarray_results (20)
Expression_cluster (160)
Interaction (303)
Map_infoMapIIIPosition-0.374015Error0.000205
PositivePositive_cloneC50C3Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
Reference (15)
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