Version: 8.0.0
Date: Tue Jan 28 2025
SOWAHD
Homo sapiensHGNC:32960
SummaryOrthologyParalogyFunction - GO AnnotationsPathwaysPhenotypesDisease AssociationsAlleles and VariantsTransgenic AllelesModelsSequence Feature ViewerSequence DetailsExpressionMolecular InteractionsGenetic Interactions
Gene

SOWAHD

Species
Homo sapiens
Symbol
SOWAHD
Name
sosondowah ankyrin repeat domain family member D
Synonyms
  • ANKRD58
  • ankyrin repeat domain 58
Biotype
protein coding gene
Automated Description
Not Available
RGD Description
ASSOCIATED WITH Autism; autistic disorder; autosomal hemophilia A; INTERACTS WITH 4,4'-sulfonyldiphenol; actinomycin D; arsane
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR14491
Stringency:
Additional filters to further constrain the results:
Species Gene symbol Count Best Best reverse
Method
Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN
Mus musculusSowahd9 of 10YesYes☑☑☑☑☐☑☑☑☑☑  
Rattus norvegicusSowahd10 of 10YesYes☑☑☑☑☑☑☑☑☑☑  
Danio reriosowahd6 of 10YesYes☑ ☑☐☐☑☐☑☑☐ ☑
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Gene symbolRank Alignment Length (aa) Similarity %Identity %Method Count
Method
Ensembl ComparaHGNCInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidSGD
SOWAHC135246324 of 8☑ ☐☐☐☑☑☑☐ 
SOWAHA232844344 of 8☑ ☐☐☐☑☑☑☐ 
SOWAHB327043314 of 8☑ ☐☐☐☑☑☑☐ 

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
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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_000023.11:g.119759217G>Avariant
    SNP
    • missense variant
    NC_000023.11:g.119759559G>Tvariant
    SNP
    • missense variant
    NC_000023.11:g.119759157C>Avariant
    SNP
    • missense variant
    NC_000023.11:g.119758743G>Avariant
    SNP
    • missense variant
    NC_000023.11:g.119759316C>Tvariant
    SNP
    • missense variant
    NC_000023.11:g.119759469G>Avariant
    SNP
    • missense variant
    NC_000023.11:g.119758674C>Gvariant
    SNP
    • missense variant
    NC_000023.11:g.119758773A>Gvariant
    SNP
    • missense variant
    NC_000023.11:g.119758853C>Gvariant
    SNP
    • missense variant
    NC_000023.11:g.119759101C>Gvariant
    SNP
    • missense variant
    Showing 1 - 10 of 19 rows
    per page
    View detailed Alleles/Variants information
    Download all Alleles/Variants for all genes of the species

    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

    No data available

    Genetic Interactions

    No data available