Br Gene Detail

Summary

• Symbol
  Br
• Name
  brachyrrhine

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:88189
  NCBI Gene: 103946
• Alliance
  gene page

Location &
Maps

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

• Genetic Map
  Chromosome 17, Syntenic
• Mapping Data
  1 experiment

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  40 phenotypes from 1 allele in 1 genetic background
  14 phenotype references
  

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

Heterozygotes have a shortened lifespan due to craniofacial and renal defects. These defects are more severe in the homozygote, resulting in neonatal lethality.

Sequences &
Gene Models

• NCBI Gene
  103946

Other
Accession IDs

MGD-MRK-1617

References

• Summaries
  All 17

  Phenotypes 14
• Earliest
  J:4539 Ma W, et al., External craniofacial features, body size, and renal morphology in prenatal brachyrrhine mice. Teratology. 1993 Apr;47(4):321-32
• Latest
  J:285676 Suzuki A, et al., Genes and microRNAs associated with mouse cleft palate: A systematic review and bioinformatics analysis. Mech Dev. 2018 Apr;150:21-27