Gene

WDR33

Species
Homo sapiens
Symbol
WDR33
Name
WD repeat domain 33
Synonyms
  • FLJ11294
  • NET14
Biotype
protein coding gene
Automated Description
Enables RNA binding activity. Predicted to be involved in postreplication repair and spermatogenesis. Located in fibrillar center and nucleoplasm.
RGD Description
This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This gene is highly expressed in testis and the protein is localized to the nucleus. This gene may play important roles in the mechanisms of cytodifferentiation and/or DNA recombination. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR22836
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Mus musculusWdr3310 of 10YesYes  
Rattus norvegicusWdr3310 of 10YesYes  
Xenopus laeviswdr33.S1 of 1YesYes           
Xenopus laeviswdr33.L1 of 1YesYes           
Xenopus tropicaliswdr339 of 9YesYes   
Danio reriowdr3310 of 10YesYes  
Drosophila melanogasterWdr338 of 9YesYes   
Caenorhabditis eleganspfs-28 of 9YesYes   
Saccharomyces cerevisiaePFS26 of 9YesYes   
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

No paralogs for the gene.

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
None
Other Sources
No data available

Disease Associations

Cases where the expected disease association was NOT found
Must provide at least one subject
Cell color indicative of annotation volume
Species
Gene
Association
Disease Qualifier
Disease
Evidence
Source
Based On
References
No records match query. Try removing filters.
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    Alleles and Variants

    Genome location
    Assembly version
    GRCh38
    Viewer Help
    Data currently unavailable; sequence viewer under construction
    Allele/Variant Symbol
    Allele Synonyms
    Category
    Variant
    Variant type
    Molecular consequence
    Has Disease Annotations
    Has Phenotype Annotations
    NC_000002.12:g.127706366G>Avariant
    SNP
    • missense variant
    NC_000002.12:g.127706412G>Avariant
    SNP
    • missense variant
    NC_000002.12:g.127702105G>Avariant
    SNP
    • missense variant
    NC_000002.12:g.127709740G>Avariant
    SNP
    • missense variant
    NC_000002.12:g.127713725G>Avariant
    SNP
    • missense variant
    NC_000002.12:g.127713821G>Avariant
    SNP
    • missense variant
    NC_000002.12:g.127714013G>Avariant
    SNP
    • missense variant
    NC_000002.12:g.127719807T>Cvariant
    SNP
    • missense variant
    NC_000002.12:g.127719932C>Tvariant
    SNP
    • missense variant
    NC_000002.12:g.127720134G>Avariant
    SNP
    • missense variant
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    Transgenic Alleles

    No data available

    Models

    No data available

    Sequence Feature Viewer

    Genome location
    Assembly version
    GRCh38
    Viewer Help
    Data currently unavailable; sequence viewer under construction

    Sequence Details

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    Expression

    Primary Sources
    None
    Other Sources
    Must provide at least one subject
    Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

    Molecular Interactions

    152 interactor genes based on 197 annotations
    WDR33 molecule type
    Interactor gene
    Interactor species
    Interactor molecule type
    Detection methods
    Source
    Reference
    protein
    AHCYL1Homo sapiens
    protein
    • affinity chromatography technology
    PMID:33961781
    protein
    AHCYL2Homo sapiens
    protein
    • affinity chromatography technology
    PMID:28514442
    protein
    AIF1Homo sapiens
    protein
    • affinity chromatography technology
    PMID:33961781
    protein
    ALG13Homo sapiens
    protein
    • proximity labelling technology
    PMID:29395067
    protein
    Anapc5Mus musculus
    protein
    • affinity chromatography technology
    PMID:26496610
    protein
    ARHomo sapiens
    protein
    • proximity labelling technology
    PMID:33640491
    protein
    ARHGAP4Homo sapiens
    protein
    • affinity chromatography technology
    PMID:32203420
    protein
    ARRDC3Homo sapiens
    protein
    • affinity chromatography technology
    PMID:38270169
    protein
    ATG16L1Homo sapiens
    protein
    • affinity chromatography technology
    PMID:30196744
    protein
    B9D2Homo sapiens
    protein
    • proximity labelling technology
    PMID:26638075
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    Genetic Interactions

    WDR33 role
    WDR33 genetic perturbation
    Interactor gene
    Interactor species
    Interactor role
    Interactor genetic perturbation
    Interaction type
    Phenotype or trait
    Source
    Reference
    unspecified role
    ATRXHomo sapiens
    unspecified role
    synthetic lethality (sensu BioGRID)
    • Growth abnormality, viability
    PMID:31551363
    unspecified role
    EGFRHomo sapiens
    unspecified role
    negative genetic interaction (sensu BioGRID)
    • Growth abnormality, viability
    PMID:34373451
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