Gene

Washc1

Species
Mus musculus
Symbol
Washc1
Name
WASH complex subunit 1
Synonyms
  • 1110049F14Rik
  • open reading frame 19
Biotype
protein coding gene
Automated Description
Enables gamma-tubulin binding activity and phosphatidylinositol 3-kinase inhibitor activity. Involved in several processes, including Arp2/3 complex-mediated actin nucleation; meiotic nuclear division; and oocyte maturation. Acts upstream of or within several processes, including low-density lipoprotein particle clearance; positive regulation of cholesterol import; and positive regulation of protein localization to cell surface. Located in autophagosome; centrosome; and endosome. Part of BLOC-1 complex and WASH complex. Is expressed in several structures, including brain; genitourinary system; immune system; liver; and lung. Orthologous to several human genes including WASHC1 (WASH complex subunit 1).
MGI Description
PHENOTYPE: Mice homozygous for a knock-out allele exhibit lethality prior to E7.5 with increased cell death and autophagy. [provided by MGI curators]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR23331
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Homo sapiensWASHC110 of 10YesYes  
Homo sapiensWASH4P8 of 10NoYes  
Homo sapiensWASH6P8 of 10NoYes  
Homo sapiensWASH2P8 of 10NoYes  
Homo sapiensWASH3P8 of 10NoYes  
Rattus norvegicusWashc19 of 9YesYes   
Xenopus tropicaliswashc19 of 9YesYes   
Danio reriowash110 of 10YesYes  
Drosophila melanogasterwash9 of 9YesYes   
Caenorhabditis elegansddl-27 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
Other Sources
Phenotype Term
Annotation details
References
abnormal amniotic cavity morphology
abnormal autophagy
abnormal ectoplacental cavity morphology
abnormal embryo development
abnormal extraembryonic coelom morphology
embryonic lethality, complete penetrance
increased cell death
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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
    GRCm39
    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
    Washc1tm1.1Ddb
    • WASHflox
    allele
    Washc1tm1.1Xyaallele
    Yes
    Washc1tm1Xya
    • WASHflox
    allele
    Yes
    Washc1tm1.2Ddballele
    Yes
    NC_000083.7:g.66418690G>Cvariant
    SNP
    • intron variant
    NC_000083.7:g.66421949C>Tvariant
    SNP
    • intron variant
    NC_000083.7:g.66423824A>Gvariant
    SNP
    • intron variant
    NC_000083.7:g.66422123A>Gvariant
    SNP
    • intron variant
    NC_000083.7:g.66423833A>Gvariant
    SNP
    • intron variant
    NC_000083.7:g.66426858A>Gvariant
    SNP
    • 3 prime UTR variant
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    Transgenic Alleles

    No data available

    Models

    Model name
    Experimental condition
    Associated Human Diseases
    Associated Phenotypes
    Modifier
    Source
    Washc1tm1.1Xya/Washc1tm1.1Xya [background:] involves: 129 * FVB/N
    • abnormal amniotic cavity morphology
    • abnormal autophagy
    MGI
    Washc1tm1.2Ddb/Washc1tm1.2Ddb [background:] involves: 129S4/SvJae * 129S4/SvJaeSor
    • embryonic lethality, complete penetrance
    MGI
    Washc1tm1Xya/Washc1tm1Xya [background:] involves: 129
    • abnormal autophagy
    MGI
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    Sequence Feature Viewer

    Genome location
    Assembly version
    GRCm39
    Viewer Help
    Data currently unavailable; sequence viewer under construction

    Sequence Details

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    Expression

    Primary Sources
    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

    33 interactor genes based on 33 annotations
    Washc1 molecule type
    Interactor gene
    Interactor species
    Interactor molecule type
    Detection methods
    Source
    Reference
    protein
    BRK1Homo sapiens
    protein
    • affinity chromatography technology
    PMID:26496610
    protein
    CAPZA1Homo sapiens
    protein
    • affinity chromatography technology
    PMID:26496610
    protein
    CAPZA2Homo sapiens
    protein
    • affinity chromatography technology
    PMID:26496610
    protein
    CAPZBHomo sapiens
    protein
    • affinity chromatography technology
    PMID:26496610
    protein
    CCDC102AHomo sapiens
    protein
    • affinity chromatography technology
    PMID:26496610
    protein
    COL4A5Homo sapiens
    protein
    • affinity chromatography technology
    PMID:26496610
    protein
    COX7A2Homo sapiens
    protein
    • affinity chromatography technology
    PMID:26496610
    protein
    CttnRattus norvegicus
    protein
    • confocal microscopy
    PMID:24344185
    protein
    Eea1Mus musculus
    protein
    • imaging technique
    PMID:29893854
    protein
    ENTR1Homo sapiens
    protein
    • affinity chromatography technology
    PMID:26496610
    Showing 1 - 10 of 33 rows
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    Genetic Interactions

    No data available