Version: 8.0.0
Date: Tue Jan 28 2025
F33H2.2
Caenorhabditis elegansWB:WBGene00009366
SummaryOrthologyParalogyFunction - GO AnnotationsPathwaysPhenotypesDisease AssociationsAlleles and VariantsTransgenic AllelesModelsSequence Feature ViewerSequence DetailsExpressionMolecular InteractionsGenetic Interactions
Gene

F33H2.2

Species
Caenorhabditis elegans
Symbol
F33H2.2
Name
Protein FAM91A1
Synonyms
  • CELE_F33H2.2
Biotype
protein coding gene
Automated Description
Orthologous to human FAM91A1 (family with sequence similarity 91 member A1).
WB Description
Enriched in several structures, including ABarpapaaa; ABplaaaaaa; ABplpaaapa; ABprpaaapa; and germ line based on tiling array; RNA-seq; and single-cell RNA-seq studies. Is affected by several genes including etr-1; hsf-1; and csr-1 based on microarray; RNA-seq; and proteomic studies. Is affected by eight chemicals including Alovudine; stavudine; and Zidovudine based on RNA-seq and microarray studies. Is predicted to encode a protein with the following domains: FAM91, C-terminal domain; FAM91; Phosphorylation site; FAM91 N-terminus; FAM91 C-terminus; and FAM91, N-terminal domain. Is an ortholog of human FAM91A1 (family with sequence similarity 91 member A1).
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR28441
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
None
Other Sources
None
Phenotype Term
Annotation details
References
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    Disease Associations

    Cases where the expected disease association was NOT found
    Cell color indicative of annotation volume
    No data available

    Alleles and Variants

    Allele/Variant Symbol
    Allele Synonyms
    Category
    Variant
    Variant type
    Molecular consequence
    Has Disease Annotations
    Has Phenotype Annotations
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      Transgenic Alleles

      Species
      (carrying the transgene)
      Allele symbol
      Transgenic construct
      Expressed components
      Knock-down targets
      Regulatory regions
      Has Disease Annotations
      Has Phenotype Annotations
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        Models

        Model name
        Experimental condition
        Associated Human Diseases
        Associated Phenotypes
        Modifier
        Source
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          Sequence Feature Viewer

          Genome location
          Assembly version
          WBcel235
          Viewer Help
          Data currently unavailable; sequence viewer under construction

          Sequence Details

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          Expression

          Primary Sources
          Other Sources
          Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

          Molecular Interactions

          F33H2.2 molecule type
          Interactor gene
          Interactor species
          Interactor molecule type
          Detection methods
          Source
          Reference
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            Genetic Interactions

            F33H2.2 role
            F33H2.2 genetic perturbation
            Interactor gene
            Interactor species
            Interactor role
            Interactor genetic perturbation
            Interaction type
            Phenotype or trait
            Source
            Reference
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