Wnt1^sw
Spontaneous Allele Detail

Summary

• Symbol: Wnt1^sw
• Name: wingless-type MMTV integration site family, member 1; swaying
• MGI ID: MGI:1856382
• Synonyms: sw
• Gene: Wnt1 Location: Chr15:98687738-98691711 bp, + strand Genetic Position: Chr15, 54.65 cM, cytoband F1-F3
• Alliance: Wnt1^sw page

Mutation origin

• Strain of Origin: STOCK Atrn^mg Edar^dl-J

Mutation description

• Allele Type: Spontaneous
• Mutation: Intragenic deletion
• Mutation details: The mutation is a deletion of 1 guanosine residue from a run of 4 consecutive guanosines beginning at genomic nucleotide 1888. This mutation is predicted to cause a frameshift mutation resulting in a stop codon 10 codons downstream from the deletion. The predicted protein would lack critical amino acids for biological activity. (J:2964)
• Inheritance: Recessive

Expression

In Mice Carrying this Mutation:	54 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: 1 strain available Cell Lines: 0 lines available
• Carrying any Wnt1 Mutation: 31 strains or lines available

References

• Original: J:15063 Lane PW, Swaying. Mouse News Lett. 1967;36:40
• All: 12 reference(s)