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WormBase Tree Display for Gene: WBGene00022253

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Name Class

WBGene00022253SMapS_parentSequenceY73B6BL
IdentityVersion2
NameCGC_namehrpf-2Person_evidenceWBPerson6228
WBPerson713
Sequence_nameY73B6BL.33
Molecular_nameY73B6BL.33a
Y73B6BL.33a.1
CE30324
Y73B6BL.33b
CE49418
Y73B6BL.33b.1
Other_nameCELE_Y73B6BL.33Accession_evidenceNDBBX284604
Public_namehrpf-2
DB_infoDatabaseAceViewgene4H138
WormQTLgeneWBGene00022253
WormFluxgeneWBGene00022253
NDBlocus_tagCELE_Y73B6BL.33
PanthergeneCAEEL|WormBase=WBGene00022253|UniProtKB=Q8MXR2
familyPTHR13976
NCBIgene177398
RefSeqproteinNM_171360.5
NM_001380274.1
TrEMBLUniProtAccQ8MXR2
V6CLR1
UniProt_GCRPUniProtAccQ8MXR2
OMIMgene300610
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:05WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
230 Mar 2009 16:33:08WBPerson9133Name_changeCGC_namehrpf-2
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classhrpf
Allele (53)
StrainWBStrain00037886
RNASeq_FPKM (74)
GO_annotation00084656
00084657
00084658
00084659
00084660
00084661
00126411
00126412
Contained_in_operonCEOP4649
Ortholog (57)
ParalogWBGene00006367Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00013703Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00020936Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable RNA binding activity. Predicted to be involved in regulation of RNA splicing. Predicted to be located in nucleoplasm. Predicted to be part of ribonucleoprotein complex. Human ortholog(s) of this gene implicated in Sjogren's syndrome; hepatocellular carcinoma; and syndromic X-linked intellectual disability. Is an ortholog of human GRSF1 (G-rich RNA sequence binding factor 1) and HNRNPF (heterogeneous nuclear ribonucleoprotein F).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:0060309Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5042)
DOID:12894Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5041)
DOID:684Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5041)
Molecular_infoCorresponding_CDSY73B6BL.33a
Y73B6BL.33b
Corresponding_transcriptY73B6BL.33a.1
Y73B6BL.33b.1
Other_sequenceJI169826.1
BMC00751_1
CBC02136_1
CRC00996_1
CR02235
JI168541.1
CBC07624_1
Associated_featureWBsf651844
WBsf667969
WBsf667970
WBsf230149
WBsf230150
WBsf230151
WBsf230152
Experimental_infoRNAi_resultWBRNAi00001671Inferred_automaticallyRNAi_primary
WBRNAi00058335Inferred_automaticallyRNAi_primary
Expr_patternExpr1014809
Expr1039813
Expr1161745
Expr2012602
Expr2030838
Drives_constructWBCnstr00024313
Construct_productWBCnstr00024313
Microarray_results (16)
Expression_cluster (116)
Interaction (105)
Map_infoMapIVPosition3.18005Error0.003706
PositivePositive_cloneY73B6BLInferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00027281
WBPaper00038491
WBPaper00055090
WBPaper00060270
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