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WormBase Tree Display for Gene: WBGene00003150

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Name Class

WBGene00003150SMapS_parentSequenceCHROMOSOME_IV
IdentityVersion1
NameCGC_namembk-2Person_evidenceWBPerson1138
Sequence_nameF49E11.1
Molecular_name (42)
Other_nameCELE_F49E11.1Accession_evidenceNDBBX284604
Public_namembk-2
DB_infoDatabaseAceViewgene4N799
WormQTLgeneWBGene00003150
SignaLinkproteinWBGene00003150
WormFluxgeneWBGene00003150
OMIMdisease190685
614104
gene600855
NDBlocus_tagCELE_F49E11.1
PanthergeneCAEEL|WormBase=WBGene00003150|UniProtKB=Q9XTF3
familyPTHR24058
NCBIgene178250
RefSeqprotein (14)
KEGGKEGG_id2.7.12.1
NemaPathKEGG_id2.7.12.1
SwissProtUniProtAccQ9XTF3
TrEMBLUniProtAccA0A061ACK4
A0A061AJ20
A0A061ACN3
A0A061ADU8
A0A061AKR6
A0A061ACN7
UniProt_GCRPUniProtAccQ9XTF3
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:30WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classmbk
Allele (429)
Strain (30)
RNASeq_FPKM (74)
GO_annotation (67)
OrthologWBGene00062706Caenorhabditis remaneiFrom_analysisOMA
TreeFam
Inparanoid_8
WormBase-Compara
WBGene00042214Caenorhabditis briggsaeFrom_analysisOrthoMCL
OMA
Inparanoid_8
WormBase-Compara
WBGene00135893Caenorhabditis japonicaFrom_analysisTreeFam
Inparanoid_8
WormBase-Compara
WBGene00192178Caenorhabditis brenneriFrom_analysisTreeFam
Inparanoid_8
WormBase-Compara
WBGene00192081Caenorhabditis brenneriFrom_analysisTreeFam
WormBase-Compara
WBGene00224493Brugia malayiFrom_analysisWormBase-Compara
CBOVI.g11096Caenorhabditis bovisFrom_analysisWormBase-Compara
CSP21.g5799Caenorhabditis parvicaudaFrom_analysisWormBase-Compara
CSP26.g18329Caenorhabditis zanzibariFrom_analysisWormBase-Compara
CSP28.g13803Caenorhabditis panamensisFrom_analysisWormBase-Compara
CSP29.g6934Caenorhabditis beceiFrom_analysisWormBase-Compara
CSP31.g13914Caenorhabditis uteleiaFrom_analysisWormBase-Compara
CSP32.g14387Caenorhabditis sulstoniFrom_analysisWormBase-Compara
CSP38.g12674Caenorhabditis quiockensisFrom_analysisWormBase-Compara
CSP39.g15491Caenorhabditis waitukubuliFrom_analysisWormBase-Compara
CSP40.g2337Caenorhabditis tribulationisFrom_analysisWormBase-Compara
Cang_2012_03_13_00161.g5961Caenorhabditis angariaFrom_analysisWormBase-Compara
Cang_2012_03_13_08380.g21469Caenorhabditis angariaFrom_analysisWormBase-Compara
Cni-mbk-2Caenorhabditis nigoniFrom_analysisWormBase-Compara
Csp11.Scaffold587.g4932Caenorhabditis tropicalisFrom_analysisWormBase-Compara
Csp5_scaffold_00041.g2172Caenorhabditis sinicaFrom_analysisWormBase-Compara
FL83_19423Caenorhabditis latensFrom_analysisWormBase-Compara
FL83_23065Caenorhabditis latensFrom_analysisWormBase-Compara
GCK72_014469Caenorhabditis remaneiFrom_analysisWormBase-Compara
OTIPU.nOt.2.0.1.g07654Oscheius tipulaeFrom_analysisWormBase-Compara
Pan_g11329Panagrellus redivivusFrom_analysisWormBase-Compara
Sp34_40148600Caenorhabditis inopinataFrom_analysisWormBase-Compara
chrIV_pilon.g12196Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00241496Onchocerca volvulusFrom_analysisWormBase-Compara
WBGene00091732Pristionchus pacificusFrom_analysisWormBase-Compara
WBGene00111526Pristionchus pacificusFrom_analysisWormBase-Compara
WBGene00265842Strongyloides rattiFrom_analysisWormBase-Compara
WBGene00291652Trichuris murisFrom_analysisWormBase-Compara
FB:FBgn0027101Drosophila melanogasterFrom_analysisOrthoFinder
OrthoInspector
Panther
PhylomeDB
SonicParanoid
ZFIN:ZDB-GENE-030131-2804Danio rerioFrom_analysisInparanoid
OrthoFinder
OrthoInspector
Panther
PhylomeDB
SonicParanoid
ZFIN:ZDB-GENE-080219-31Danio rerioFrom_analysisEnsEMBL-Compara
Inparanoid
OrthoFinder
OrthoInspector
Panther
SonicParanoid
HGNC:3094Homo sapiensFrom_analysisEnsEMBL-Compara
Inparanoid
OrthoFinder
OrthoInspector
Panther
SonicParanoid
HGNC:3093Homo sapiensFrom_analysisInparanoid
OrthoFinder
OrthoInspector
Panther
PhylomeDB
SonicParanoid
MGI:1330301Mus musculusFrom_analysisInparanoid
OrthoFinder
OrthoInspector
Panther
PhylomeDB
SonicParanoid
MGI:1330300Mus musculusFrom_analysisEnsEMBL-Compara
Inparanoid
OrthoFinder
OrthoInspector
Panther
SonicParanoid
RGD:1310924Rattus norvegicusFrom_analysisEnsEMBL-Compara
Inparanoid
OrthoFinder
OrthoInspector
Panther
SonicParanoid
RGD:1312039Rattus norvegicusFrom_analysisInparanoid
OrthoFinder
OrthoInspector
Panther
PhylomeDB
SonicParanoid
ParalogWBGene00001994Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003149Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00016465Caenorhabditis elegansFrom_analysisTreeFam
Panther
WBGene00016464Caenorhabditis elegansFrom_analysisTreeFam
Panther
WBGene00006517Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00013727Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00185089Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionmbk-2 encodes one of two C. elegans members of the DYRK (dual-specificity Yak1-related kinase) family of proteins that includes S. cerevisiae Yak1 and the Drosophila minibrain and DYRK2 kinases; MBK-2 activity is required maternally for the oocyte-to-egg transition that occurs during the earliest stages of embryonic development; specifically, MBK-2 is required for: 1) posterior localization of the germ plasm components PIE-1, POS-1, and PGL-1, and 2) post-fertilization degradation of a subset of maternal proteins including the MEI-1 and MEI-2 meiosis-specific katanin subunits, the OMA-1 oocyte maturation factor, and residual PIE-1 that remains anteriorly localized after its normal posterior segregation; MBK-2 also primes the MEX-5 polarity protein for subsequent phosphorylation by the polo-like kinase PLK-1; genetic analyses suggest that, in regulating the segregation and degradation of maternal proteins, MBK-2 lies downstream of the initial embryonic polarity cues established by the PAR and MEX proteins; MBK-2 activity depends upon progression through the meiotic divisions and is positively regulated by CDK-1 and negatively regulated by EGG-3 and EGG-4/5; MBK-2 physically interacts with EGG-3 and EGG-4, suggesting that regulation by EGG-3 and EGG-4 is direct; MBK-2 is expressed uniformly in the cortex of oocytes and newly fertilized zygotes; in later stage zygotes, just prior to the second meiotic division, MBK-2 becomes localized to discrete cortical foci, and by the first mitosis it is found predominantly on centrosomes and chromosomes; MBK-2 is also associated with P granules in the germline blastomeres P2, P3, and P4.Paper_evidenceWBPaper00006085
WBPaper00006352
WBPaper00026970
WBPaper00026975
WBPaper00027607
WBPaper00031434
WBPaper00035427
Curator_confirmedWBPerson1843
Date_last_updated02 Mar 2011 00:00:00
Automated_descriptionEnables protein serine/threonine kinase activity and protein tyrosine kinase activity. Involved in several processes, including P granule disassembly; asymmetric protein localization involved in cell fate determination; and positive regulation of proteasomal ubiquitin-dependent protein catabolic process. Located in cell cortex and intracellular non-membrane-bounded organelle. Expressed in several structures, including body wall musculature; embryonic cell; gonad; oocyte; and pharynx. Used to study Down syndrome. Is an ortholog of human DYRK2 (dual specificity tyrosine phosphorylation regulated kinase 2) and DYRK3 (dual specificity tyrosine phosphorylation regulated 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_infoExperimental_modelDOID:14250Homo sapiensPaper_evidenceWBPaper00005756
Accession_evidenceOMIM190685
614104
Curator_confirmedWBPerson324
Date_last_updated05 Jun 2017 00:00:00
Disease_relevanceHuman DYRK1A gene encodes a member of the dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) family, which includes Drosophila minibrain, and is a conserved gene located in the Down Syndrome critical region (DSCR) of chromosome 21; Down syndrome is the most frequent chromosomal abnormality in human infants, where DYRK1A overexpression is observed, and is characterized by a set of facial and physical features, heart defects, abnormalities in the immune and endocrine systems, spatial memory defecits and difficulty in converting short-term to long-term memories; in elegans, the genes mbk-1 and mbk-2 have close homology with human DYRK1A and hpk-1 is more distantly related; while mutants deficient for mbk-1 seem to be normal, overexpression of mbk-1 causes behavioral defects in chemotaxis, acting in mature, fully differentiated neurons; however, this defect could be reversed by bringing back normal mbk-1 levels, which provided the first hint that DYRK1-induced defects could be reversed; mbk-2(pk1427) homozygous animals display 100% penetrant maternal-effect embryonic lethality, making it difficult to test redundant function with mbk-1.Homo sapiensPaper_evidenceWBPaper00005756
Accession_evidenceOMIM600855
Curator_confirmedWBPerson324
Date_last_updated05 Jun 2017 00:00:00
Models_disease_assertedWBDOannot00000129
Molecular_infoCorresponding_CDS (14)
Corresponding_transcript (14)
Other_sequence (53)
Associated_feature (76)
Experimental_infoRNAi_result (38)
Expr_pattern (13)
Drives_constructWBCnstr00000360
WBCnstr00000362
WBCnstr00011276
WBCnstr00012087
Construct_productWBCnstr00000083
WBCnstr00000084
WBCnstr00000088
WBCnstr00000362
WBCnstr00000364
WBCnstr00010903
WBCnstr00011276
WBCnstr00011667
WBCnstr00012087
AntibodyWBAntibody00001303
WBAntibody00001304
Microarray_results (61)
Expression_cluster (155)
Interaction (272)
Map_infoMapIVPosition6.86808Error0.065322
PositivePositive_cloneF49E11Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4484
Pseudo_map_position
Reference (64)
RemarkSequence connection from [Raich WB]. 02/06/12 krb.
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