Gene

Amh

Species
Mus musculus
Symbol
Amh
Name
anti-Mullerian hormone
Synonyms
  • MIS
  • Mullerian inhibiting substance
Biotype
protein coding gene
Automated Description
Predicted to enable type II transforming growth factor beta receptor binding activity. Involved in gonad development; negative regulation of ovarian follicle development; and sex determination. Located in cytoplasm. Is expressed in several structures, including aorta-gonad-mesonephros; genitourinary system; liver; lung; and spleen. Human ortholog(s) of this gene implicated in disorder of sexual development; ovarian carcinoma; and persistent Mullerian duct syndrome. Orthologous to human AMH (anti-Mullerian hormone).
MGI Description
PHENOTYPE: Homozygous null mutant males have a complete male reproductive tract and functional sperm, but also uterus and oviducts. Most are infertile due to female organs blocking sperm transfer. Females are fertile with enlarged ovaries and atypical follicles. [provided by MGI curators]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR15009
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

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Annotation details
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    Disease Associations

    Cases where the expected disease association was NOT found
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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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          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

          Amh molecule type
          Interactor gene
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            Genetic Interactions

            Amh role
            Amh genetic perturbation
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