Sall4^tm1Ryn
Targeted Allele Detail

Summary

• Symbol: Sall4^tm1Ryn
• Name: spalt like transcription factor 4; targeted mutation 1, Ryuichi Nishinakamura
• MGI ID: MGI:3699175
• Synonyms: Sall4-del
• Gene: Sall4 Location: Chr2:168590252-168609121 bp, - strand Genetic Position: Chr2, 88.99 cM
• Alliance: Sall4^tm1Ryn page

Mutation origin

• Germline Transmission: Earliest citation of germline transmission: J:118119
• Parent Cell Line: E14.1 (ES Cell)
• Strain of Origin: 129P2/OlaHsd

Mutation description

• Allele Type: Targeted (Null/knockout)
• Mutations: Insertion, Intragenic deletion
• Mutation details: The entire coding region was deleted and replaced with beta-galactosidase and neomycin resistance genes. The mutation removes all eight zinc finger domains from the gene and results in the fusion of 39 amino acids at the N terminal of Sall4 and beta-galactosidase. Although a beta-galactosidase gene was inserted, lacZ is not expressed. (J:118119)

Disease models

Expression

In Mice Carrying this Mutation:	14 assay results
In Structures Affected by this Mutation:	6 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 Sall4 Mutation: 145 strains or lines available

References

• Original: J:118119 Sakaki-Yumoto M, et al., The murine homolog of SALL4, a causative gene in Okihiro syndrome, is essential for embryonic stem cell proliferation, and cooperates with Sall1 in anorectal, heart, brain and kidney development. Development. 2006 Aug;133(15):3005-13
• All: 1 reference(s)