Gene

tmem38b

Species
Danio rerio
Symbol
tmem38b
Name
transmembrane protein 38B
Synonyms
  • zgc:55815
Biotype
protein coding gene
Automated Description
Predicted to enable potassium channel activity. Acts upstream of or within fin regeneration; regulation of bone development; and regulation of bone mineralization. Predicted to be located in endoplasmic reticulum. Is expressed in brain; heart; muscle; skeletal system; and swim bladder. Human ortholog(s) of this gene implicated in osteogenesis imperfecta type 14. Orthologous to human TMEM38B (transmembrane protein 38B).
ZFIN Description
Not Available
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR12454

Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
Other Sources
None
Phenotype Term
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

    Allele/Variant Symbol
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    Variant type
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      Transgenic Alleles

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

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          Sequence Feature Viewer

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          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

          tmem38b molecule type
          Interactor gene
          Interactor species
          Interactor molecule type
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            Genetic Interactions

            tmem38b role
            tmem38b genetic perturbation
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