Nil Gene Detail

Summary

• Symbol
  Nil
• Name
  neonatal intestinal lipidosis
• Synonyms
  Ml

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:97343
  NCBI Gene: 110093
• Alliance
  gene page

Location &
Maps

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

• Genetic Map
  Chromosome 7, Syntenic
• Mapping Data
  1 experiment

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  8 phenotypes from 1 allele in 1 genetic background
  3 phenotype references
  

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

Mutations in this gene are lethal for the homozygote and cause lipidosis of the small intestine in the heterozygote.

Sequences &
Gene Models

• NCBI Gene
  110093

Other
Accession IDs

MGD-MRK-12251, MGD-MRK-12879

References

• Summaries
  All 9

  Phenotypes 3
• Earliest
  J:5144 Wallace ME, et al., Neonatal intestinal lipidosis in mice. An inherited disorder of the intestinal lymphatic vessels. J Med Genet. 1969 Dec;6(4):361-75
• Latest
  J:5917 Doolittle DP, et al., Myelin deficient, a new neurological mutant in the mouse. J Hered. 1977 Sep-Oct;68(5):331-2