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Scs
Spontaneous Allele Detail
Summary
Symbol: Scs
Name: semi-dominant compacted skeleton
MGI ID: MGI:5517547
Gene: Scs  Location: unknown  Genetic Position: Chr5, Syntenic
Alliance: Scs page
Abnormal axial skeleton morphology and short tail in Scs/+ mouse

Show the 2 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  C3H/HeDiSn-Dscam2J/GrsrJ
Mutation
description
Allele Type:    Spontaneous
Mutation:    Undefined
    This heritable phenotype arose spontaneously and has been mapped to Chromosome 5. (J:202091)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 5 anatomical structure(s)
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 Scs Mutation:  1 strain or line available
References
Original:  J:202091 Harris BS, et al., A new skeletal mutation named semi-dominant compacted skeleton that maps to Chromosome 5. MGI Direct Data Submission. 2013;
All:  1 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
04/23/2024
MGI 6.23
The Jackson Laboratory