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Heritable Phenotypic Marker : Bey bulgy-eye

Primary Identifier	MGI:1276118	Organism	mouse, laboratory
Chromosome	7	Mgi Type	heritable phenotypic marker

description

FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Used to study Crouzon syndrome.
PHENOTYPE: Homozygous lethal; heterozygotes are fertile, have a squat face and bulging eyes due to facial shortening and craniosynostosis. [provided by MGI curators]

synonyms:
bulgy-eye,
Bey

earliestPublication:
Carlton MB, et al. (1998) Crouzon-like craniofacial dysmorphology in the mouse is caused by an insertional mutation at the Fgf3/Fgf4 locus. Dev Dyn 212(2):242-9

Features --> Cross References

Genome

Sequence Feature Displayer

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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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