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

Symbol:	Atp2b2dfw
Name:	ATPase, Ca++ transporting, plasma membrane 2; deaf waddler
MGI ID:	MGI:1856799
Synonyms:	deafwaddler, dfw
Gene:	Atp2b2  Location: Chr6:113720803-114019574 bp, - strand  Genetic Position: Chr6, 52.85 cM
Alliance:	Atp2b2dfw page

Strain of Origin:

C3H/HeJ

Allele Type:    Spontaneous Mutation:    Single point mutation   Mutation details: A G to A transition point mutation at position 847 is predicted to cause a glycine to serine substitution at position 283 in the encoded protein. (J:48969) Inheritance:    Recessive

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

In Structures Affected by this Mutation:

4 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 Atp2b2 Mutation:	66 strains or lines available

Original:	J:14114 Lane PW, Deaf waddler (dfw). Mouse News Lett. 1987;77:129
All:	10 reference(s)