Gene

Fhl2

Species
Mus musculus
Symbol
Fhl2
Name
four and a half LIM domains 2
Synonyms
  • C76204
  • expressed sequence C76204
Biotype
protein coding gene
Automated Description
Enables bHLH transcription factor binding activity and transcription corepressor activity. Involved in several processes, including heart development; negative regulation of calcineurin-NFAT signaling cascade; and osteoblast differentiation. Acts upstream of or within regulation of transcription by RNA polymerase II. Located in Z disc and nucleus. Is expressed in several structures, including alimentary system; cardiovascular system; central nervous system; periodontal ligament; and urinary system. Orthologous to human FHL2 (four and a half LIM domains 2).
MGI Description
PHENOTYPE: Mice homozygous for a targeted null mutation display osteopenia and osteoporosis; cardiovascular development is normal but cardiac hypertrophy develops in mutants in response to beta-adrenergic stimulation. [provided by MGI curators]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR24205
No data available
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Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

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Annotation details
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    Disease Associations

    Cases where the expected disease association was NOT found
    Cell color indicative of annotation volume
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      Alleles and Variants

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        Transgenic Alleles

        Species
        (carrying the transgene)
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        Transgenic construct
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          Models

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            Sequence Feature Viewer

            Genome location
            Assembly version
            GRCm39
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            43.17M43.18M43.19M43.20M43.21M43.22M43.23M

            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

            Fhl2 molecule type
            Interactor gene
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              Genetic Interactions

              Fhl2 role
              Fhl2 genetic perturbation
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