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nt
Spontaneous Allele Detail
Summary
Symbol: nt
Name: no turning deletion region; no turning
MGI ID: MGI:1857804
Gene: nt  Location: unknown  Genetic Position: Chr18, Syntenic
Alliance: nt page
Mutation
origin
Strain of Origin:  CD-1
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intergenic deletion
  nt involves 18 genes/genome features (Gm22694, Rttn, Mir6359 ...) View all
 
Mutation detailsThis spontaneous mutation was found in a CD-1 colony at the University of Pennsylvania in 1998. The mutation is a 1.6Mb deletion on chromosome 18 that includes the Rttn, Cd226, Dok6 and the Txndc10 genes. (J:132045)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 26 assay results
In Structures Affected by this Mutation: 8 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 nt Mutation:  0 strains or lines available
References
Original:  J:45709 Melloy PG, et al., No turning, a mouse mutation causing left-right and axial patterning defects. Dev Biol. 1998 Jan 1;193(1):77-89
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
04/16/2024
MGI 6.23
The Jackson Laboratory