Bey Gene Detail

Summary

• Symbol
  Bey
• Name
  bulgy-eye

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:1276118
  NCBI Gene: 109576
• Alliance
  gene page

Location &
Maps

• Sequence Map
  Genome coordinates not available from the current reference assembly.

• Genetic Map
  Chromosome 7, Syntenic
• Mapping Data
  2 experiments

Strain
Comparison

• RFLP
  1

Human Diseases

• Diseases
  1 with Bey mouse models

Human Disease

Mouse Models

Crouzon syndrome

IDs

Crouzon syndrome      

DOID:2339
ICD10CM:Q75.1
MESH:D003394
NCI:C84653
OMIM:123500
UMLS_CUI:C0010273

View 1 model

Mouse Models

Human Disease Modeled: Crouzon syndrome

Allelic Composition	Genetic Background	Reference	Phenotypes
Bey/Bey+	129S/SvEv-Bey	J:47965	View

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

• Phenotype Summary
  15 phenotypes from 1 allele in 1 genetic background
  1 phenotype reference
  

• All Mutations and Alleles
  1
• Find Mice (IMSR)
  0 strains or lines available

Homozygous lethal; heterozygotes are fertile, have a squat face and bulging eyes due to facial shortening and craniosynostosis.

Sequences &
Gene Models

• NCBI Gene
  109576

Molecular
Reagents

• All nucleic 4

  Genomic 4

References

• 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