hug Gene Detail

Summary

• Symbol
  hug
• Name
  hugger

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:96287
  NCBI Gene: 15573
• Alliance
  gene page

Location &
Maps

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

• Genetic Map
  Chromosome 19, Syntenic
• Mapping Data
  4 experiments

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  12 phenotypes from 1 allele in 1 genetic background
  3 images
  2 phenotype references
  

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

Homozygotes for a spontaneous mutation exhibit distinctive locomotor abnormalities, progressive retinal degeneration and photoreceptor cell loss, and impaired breeding in both males and females.

Sequences &
Gene Models

• NCBI Gene
  15573

Other
Accession IDs

MGD-MRK-11015

References

• Summaries
  All 3

  Phenotypes 2
• Earliest
  J:40666 Sidman RL, et al., Mapping and retinal phenotype of the hugger mutation in the mouse. Mamm Genome. 1997 Jun;8(6):399-402