Gene

Mab21l1

Species
Mus musculus
Symbol
Mab21l1
Name
mab-21-like 1
Synonyms
  • AW047968
  • expressed sequence AW047968
Biotype
protein coding gene
Automated Description
Predicted to enable metal ion binding activity; nucleotide binding activity; and nucleotidyltransferase activity. Acts upstream of or within camera-type eye development and positive regulation of cell population proliferation. Located in nucleus. Is expressed in several structures, including branchial arch; central nervous system; limb bud; maxillary process; and sensory organ. Orthologous to human MAB21L1 (mab-21 like 1).
MGI Description
PHENOTYPE: Homozygous mutation of this gene results in male infertility and eye developmental anomalies. Mutant eyes are small, absent of lens and iris, and display malformations of the retina. [provided by MGI curators]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR10656
No data available
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Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

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Other Sources
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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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          Models

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            Sequence Feature Viewer

            Genome location
            Assembly version
            GRCm39
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            55.6900M55.6902M55.6904M55.6906M55.6908M55.6910M55.6912M55.6914M55.6916M55.6918M55.6920M55.6922M55.6924M

            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

            Mab21l1 molecule type
            Interactor gene
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              Genetic Interactions

              Mab21l1 role
              Mab21l1 genetic perturbation
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