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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
more
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 7, Syntenic
  • Mapping Data
    1 experiment
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    8 phenotypes from 1 allele in 1 genetic background
    3 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
Mutations in this gene are lethal for the homozygote and cause lipidosis of the small intestine in the heterozygote.
Sequences &
Gene Models
less
Other
Accession IDs
less
MGD-MRK-12251, MGD-MRK-12879
References
more
  • 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
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Funding Information
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Send questions and comments to User Support. 		last database update
05/07/2024
MGI 6.23 		The Jackson Laboratory