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Del(17)TOrl
Spontaneous Allele Detail
Nomenclature
Symbol: Del(17)TOrl
Name: deletion, Chr 17, TOrl, T-Orleans
MGI ID: MGI:1856189
Synonyms: TOrl, TtOrl
Gene: Del(17)TOrl  Location: unknown  Genetic Position: Chr17, Syntenic
Mutation
origin
Strain of Origin:  Orl:Swiss
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intergenic deletion
 
Mutation detailsThe deletion comprising this allele includes T through, at least, Qk as all short-tailed mice from matings of TOrl/+ males to Qkqk/Qkqk females have a "quaking" phenotype. In addition this allele expresses the t- haplotype specific proteins p63/6.9a, TCP-4B, TCP-5, TCP-9, and TCP-8B. (J:6957)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 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 Del(17)TOrl Mutation:  1 strain or line available
References
Original:  J:15078 Moutier R, t. Mouse News Lett. 1973;49:42
All:  5 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
03/30/2021
MGI 6.16
The Jackson Laboratory