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snol
Spontaneous Allele Detail
Nomenclature
Symbol: snol
Name: snubnose-like
MGI ID: MGI:2449570
Gene: snol  Location: unknown  Genetic Position: Chr4, Syntenic
Short nose, and odd face and body shape in a snol/snol mouse (right) compared to sibling control (left)

Show the 1 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  C3H/HeJ
Mutation
description
Allele Type:    Spontaneous
Mutation:    Undefined
    A spontaneous mutation discovered at The Jackson Laboratory.
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 3 anatomical structures
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any snol Mutation:  1 strain or line available
Notes

A short nosed mutation, snubnose (sno), maps in this location, but could not be allele tested because it is believed to be extinct. The spina bifida occulta reported in sno is not seen in snol.

References
Original:  J:78986 Ward-Bailey PF, et al., Snubnose-like (snol): a new spontaneous skeletal mutation on Chromosome 4 in the mouse. Mouse Mutant Resources Web Site, The Jackson Laboratory, Bar Harbor, Maine. MGI Direct Data Submission. 2002;
All:  2 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)
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last database update
07/07/2020
MGI 6.15
The Jackson Laboratory