hsh Gene Detail

Summary

• Symbol
  hsh
• Name
  hind shaker

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:1096571
  NCBI Gene: 15501
• Alliance
  gene page

Location &
Maps

• Sequence Map
  Chr3:87170454-90267085 bp

  From MGI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 3, Syntenic
• Mapping Data
  2 experiments

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  3 phenotype references
  

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

Sequences &
Gene Models

• NCBI Gene
  15501

References

• Summaries
  All 5

  Phenotypes 3
• Earliest
  J:43545 King H, et al., Hindshaker, a novel myelin mutant showing hypomyelination preferentially affecting the spinal cord. J Neurocytol. 1997 Aug;26(8):557-66
• Latest
  J:87785 Karim SA, et al., A physical map of the genomic region on mouse chromosome 3 containing the hindshaker (hsh) mutation. Genomics. 2004 Feb;83(2):225-30