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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
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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:  26 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)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory