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WormBase Tree Display for Gene: WBGene00001526

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Name Class

WBGene00001526SMapS_parentSequenceT19A5
IdentityVersion1
NameCGC_namegck-1Person_evidenceWBPerson565
Sequence_nameT19A5.2
Molecular_name (24)
Other_nameCELE_T19A5.2Accession_evidenceNDBBX284605
Public_namegck-1
DB_infoDatabase (14)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:24WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classgck
Allele (115)
StrainWBStrain00022765
WBStrain00035558
WBStrain00034752
RNASeq_FPKM (74)
GO_annotation (35)
Contained_in_operonCEOP5569
Ortholog (41)
Paralog (27)
Structured_descriptionConcise_descriptiongck-1 encodes one of eight C. elegans germinal center kinases (GCKs) that are members of the Ste20-related family of kinases; GCK-1 is the sole C. elegans GCK-III subfamily member; during reproductive development, GCK-1 functions in the germ line to regulate oocyte development by inhibiting activation of a specific MPK-1 isoform, MPK-1a, and by negatively regulating physiological germline apoptosis; GCK-1 physically interacts with MPK-1a in vitro suggesting that, in vivo, GCK-1 inhibits MPK-1a by a direct interaction.Paper_evidenceWBPaper00035301
Curator_confirmedWBPerson48
WBPerson1843
Date_last_updated15 Oct 2009 00:00:00
Automated_descriptionEnables mitogen-activated protein kinase binding activity and protein serine/threonine kinase activity. Involved in several processes, including positive regulation of GTPase activity; positive regulation of endocytic recycling; and regulation of oocyte development. Located in cytoplasm and cytoplasmic side of apical plasma membrane. Used to study cerebral cavernous malformation. Is an ortholog of human STK26 (serine/threonine kinase 26).Paper_evidenceWBPaper00065943
WBPaper00067038
Curator_confirmedWBPerson324
WBPerson37462
Inferred_automaticallyThis description was generated automatically by a script based on data from the WS296 version of WormBase
Date_last_updated20 Mar 2025 00:00:00
Disease_infoExperimental_modelDOID:0060669Homo sapiensPaper_evidenceWBPaper00046519
Curator_confirmedWBPerson324
Date_last_updated24 Sep 2020 00:00:00
Models_disease_in_annotationWBDOannot00000810
Molecular_infoCorresponding_CDST19A5.2a
T19A5.2b
T19A5.2c
T19A5.2d
T19A5.2e
T19A5.2f
T19A5.2g
T19A5.2h
Corresponding_CDS_historyT19A5.2b:wp239
T19A5.2c:wp239
Corresponding_transcriptT19A5.2a.1
T19A5.2b.1
T19A5.2c.1
T19A5.2d.1
T19A5.2e.1
T19A5.2f.1
T19A5.2g.1
T19A5.2h.1
Other_sequence (45)
Associated_feature (20)
Experimental_infoRNAi_result (19)
Expr_patternExpr1011654
Expr1030918
Expr1157045
Expr1200202
Expr2011962
Expr2030199
Drives_constructWBCnstr00036888
Construct_productWBCnstr00036888
Microarray_results (49)
Expression_cluster (103)
Interaction (71)
Map_infoMapVPosition1.87047Error0.002963
PositivePositive_cloneT19A5Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4336
Pseudo_map_position
Reference (23)
RemarkSequence connection from [Schumacher JM]
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