Summary | Mutation origin | Mutation description | Expression | Phenotypes | Find Mice (IMSR) | References

Symbol:	Wnt1sw
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:	Wnt1sw page

Strain of Origin:

STOCK Atrnmg Edardl-J

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

View phenotypes and curated references for all genotypes (concatenated display).

In Mice Carrying this Mutation:	54 assay results
In Structures Affected by this Mutation:	6 anatomical structure(s)

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:	30 strains or lines available

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