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Ap3d1mh
Spontaneous Allele Detail
Summary
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
Mutation
origin
Strain of Origin:  B6.C3-Grxcr1pi
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intragenic deletion
 
Mutation detailsThe 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
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 13 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 Ap3d1 Mutation:  79 strains or lines available
References
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)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory