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Bey Gene Detail
Summary
  • Symbol
    Bey
  • Name
    bulgy-eye
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:1276118
    NCBI Gene: 109576
Location & Maps
more
  • Sequence Map
    Genome coordinates not available
  • Genetic Map
    Chromosome 7, Syntenic
  • Mapping Data
    2 experiments
Human Diseases
more
  • Diseases
    1 with Bey mouse models

Human Disease Mouse Models
       Crouzon Syndrome   OMIM: 123500 View 1 model
Click on a disease name to see all genes associated with that disease.

  • Mutations/Alleles
    1 with disease annotations
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    8 phenotypes from 1 allele in 1 genetic background
    1 phenotype reference
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
Homozygous lethal; heterozygotes are fertile, have a squat face and bulging eyes due to facial shortening and craniosynostosis.
Sequences &
Gene Models
less
Polymorphisms
less
  • RFLP
Molecular
Reagents
less
  • All nucleic 4
    Genomic 4
References
more
  • Summaries
    All 2
    Diseases 1
    Phenotypes 1
  • Earliest
    J:47965 Carlton MB, et al., Crouzon-like craniofacial dysmorphology in the mouse is caused by an insertional mutation at the Fgf3/Fgf4 locus. Dev Dyn. 1998 Jun;212(2):242-9

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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last database update
11/29/2016
MGI 6.06
The Jackson Laboratory