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WormBase Tree Display for Gene: WBGene00017472

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Name Class

WBGene00017472SMapS_parentSequenceF14H12
IdentityVersion2
NameCGC_namecst-1Person_evidenceWBPerson1787
Sequence_nameF14H12.4
Molecular_nameF14H12.4a
F14H12.4a.1
CE39916
F14H12.4b
CE39917
F14H12.4b.1
Other_namecMSTPaper_evidenceWBPaper00046589
CELE_F14H12.4Accession_evidenceNDBBX284606
Public_namecst-1
DB_infoDatabase (14)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:58WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
230 Jun 2006 11:51:09WBPerson2970Name_changeCGC_namecst-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classcst
Allele (42)
RNASeq_FPKM (74)
GO_annotation (23)
Ortholog (36)
Paralog (27)
Structured_descriptionConcise_descriptioncst-1 encodes one of two C. elegans protein kinases orthologous to the MST (mammalian Ste20-like) kinases and Drosophila Hippo; CST-1 appears to play a role in the responses to oxidative stress and determination of adult lifespan; in regulating stress response and lifespan, CST-1 functions upstream of the DAF-16/FOXO transcription factor; CST-1 physically interacts with RSF-1, the C. elegans homolog of the Ras-association domain family protein 1.Paper_evidenceWBPaper00027662
WBPaper00041685
Curator_confirmedWBPerson1843
Date_last_updated12 Mar 2013 00:00:00
Automated_descriptionPredicted to enable protein serine/threonine kinase activity. Involved in determination of adult lifespan and muscle cell development. Predicted to be located in cytoplasm. Expressed in hypodermis; sensory neurons; terminal bulb; and vulva. Human ortholog(s) of this gene implicated in primary immunodeficiency disease. Is an ortholog of human STK3 (serine/threonine kinase 3).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:612Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11408)
Molecular_infoCorresponding_CDSF14H12.4a
F14H12.4b
Corresponding_CDS_historyF14H12.4a:wp155
F14H12.4b:wp155
Corresponding_transcriptF14H12.4a.1
F14H12.4b.1
Other_sequence (44)
Associated_featureWBsf1004907
WBsf1004908
WBsf1022768
WBsf1022769
WBsf235569
WBsf235570
Experimental_infoRNAi_result (11)
Expr_patternExpr3929
Expr13233
Expr1148618
Expr2010562
Expr2028802
Drives_constructWBCnstr00011754
WBCnstr00015996
WBCnstr00027271
WBCnstr00038935
Construct_productWBCnstr00015996
WBCnstr00027271
WBCnstr00038935
Microarray_results (14)
Expression_cluster (87)
Interaction (13)
Map_infoMapXPosition-7.77494Error0.003139
PositivePositive_cloneF14H12Inferred_automaticallyFrom sequence, transcript, pseudogene data
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