About   Help   FAQ
Nil
Spontaneous Allele Detail
Summary
Symbol: Nil
Name: neonatal intestinal lipidosis
MGI ID: MGI:1861185
Synonyms: Ml
Gene: Nil  Location: unknown  Genetic Position: Chr7, Syntenic
Alliance: Nil page
Mutation
origin
Strain of Origin:  A/Cam
Mutation
description
Allele Type:    Spontaneous
Inheritance:    Semidominant
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 3 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Nil Mutation:  0 strains or lines available
Notes
This mutation is extinct.
References
Original:  J:33328 Wallace ME, Milky (ml), a new mutant (now = Nil). Mouse News Lett. 1963;28:22
All:  3 reference(s)

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
10/29/2024
MGI 6.24
The Jackson Laboratory