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

Symbol:	Atp2b2dfw-2J
Name:	ATPase, Ca++ transporting, plasma membrane 2; deaf waddler 2 Jackson
MGI ID:	MGI:1857396
Synonyms:	dfw-2J
Gene:	Atp2b2  Location: Chr6:113720803-114019574 bp, - strand  Genetic Position: Chr6, 52.85 cM
Alliance:	Atp2b2dfw-2J page

Strain of Origin:

CByJ.A-Ttc7fsn/J

Allele Type:    Spontaneous Mutation:    Intragenic deletion   Mutation details: A 2 bp nucleotide deletion at positions 1368 and 1369 cause a frameshift that results in a premature stop and truncation of the encoded protein at position 471. (J:48969) Inheritance:    Recessive

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

In Structures Affected by this Mutation:

2 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:38429 Noben-Trauth K, et al., mdfw: a deafness susceptibility locus that interacts with deaf waddler (dfw). Genomics. 1997 Sep 15;44(3):266-72
All:	12 reference(s)