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Heritable Phenotypic Marker : sau sauron
Primary Identifier  MGI:3607718 Organism  mouse, laboratory
Chromosome  13 Mgi Type  heritable phenotypic marker
description  PHENOTYPE: Most embryos hemizygous (opposite the Del(13)36H on the homologous chromosome) for the mutation die by embryonic day E16.5. Holoprocencephaly is observed among embryonic and surviving neonatal hemizygotes. Heterozygous mice exhibit elevated anxiety. [provided by MGI curators]
  • synonyms:
  • sauron,
  • sau,
  • 1239
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Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Involved In Mutations

0 Transgenic Expressors

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For





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