About   Help   FAQ
Sox18Ragl
Spontaneous Allele Detail
Summary
Symbol: Sox18Ragl
Name: SRY (sex determining region Y)-box 18; ragged-like
MGI ID: MGI:1889617
Synonyms: Ragl
Gene: Sox18  Location: Chr2:181311630-181313433 bp, - strand  Genetic Position: Chr2, 103.71 cM
Alliance: Sox18Ragl page
Mutation
origin
Strain of Origin:  (C57BL/6J-Aw-J x 129P3/J)F1/J
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intragenic deletion
 
Mutation detailsA spontaneous mouse mutant phenotypically similar to the ragged mouse. The mutation was identified as a deletion of a single guanine reported as nucleotide 937 in J:74211 and as nucleotide 970 causing truncation of the transcriptional trans-activation domain in J:83731. (J:74211, J:83731)
Inheritance:    Dominant
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 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 Sox18 Mutation:  25 strains or lines available
References
Original:  J:51014 Donahue LR, The Jackson Laboratory Mouse Mutant Resource 1999 Mutation Reports. MGI Direct Data Submission. 1999;
All:  4 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
04/16/2024
MGI 6.23
The Jackson Laboratory