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

Symbol:	Ap3d1mh
Name:	adaptor-related protein complex 3, delta 1 subunit; mocha
MGI ID:	MGI:1856083
Synonyms:	mh, mocha
Gene:	Ap3d1  Location: Chr10:80542790-80578098 bp, - strand  Genetic Position: Chr10, 39.72 cM
Alliance:	Ap3d1mh page

Strain of Origin:

B6.C3-Grxcr1pi

Allele Type:    Spontaneous Mutation:    Intragenic deletion   Mutation details: The mutation is a 12 kb deletion that removes at least two exons, resulting in a 496 bp deletion of coding material shortly after the initiating ATG codon and causing an out of frame translation followed by a premature termination site. (J:50662) Inheritance:    Recessive

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

In Structures Affected by this Mutation:

12 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 Ap3d1 Mutation:	79 strains or lines available

Original:	J:5511 Lane PW, et al., Mocha, a new coat color and behavior mutation on chromosome 10 of the mouse. J Hered. 1974 Nov-Dec;65(6):362-4
All:	35 reference(s)