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Atp7aMo-11H
Chemically and radiation induced Allele Detail
Summary
Symbol: Atp7aMo-11H
Name: ATPase, copper transporting, alpha polypeptide; mottled 11 Harwell
MGI ID: MGI:1856323
Synonyms: Atp7amo11H
Gene: Atp7a  Location: ChrX:105070882-105168532 bp, + strand  Genetic Position: ChrX, 47.36 cM
Alliance: Atp7aMo-11H page
Mutation
origin
Strain of Origin:  (C3H/HeH x 101/H)F1
Mutation
description
Allele Type:    Chemically and radiation induced
Mutation:    Single point mutation
 
Mutation detailsThis mutation arose in mutagenesis studies at Harwell. Molecular analysis detected a C to A transversion mutation at position 4173 that alters codon 1364 from alanine to aspartate. (J:38977)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Atp7a Mutation:  69 strains or lines available
Notes
The mutation was derived from a mutagenized male that had been treated with both hydroxyurea and X-rays.
References
Original:  J:16303 Rasberry C, et al., Three new mottled mutations - Mo10H, Mo11H, and Mo12H. Mouse Genome. 1993;91(4):851-53
All:  3 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
12/10/2024
MGI 6.24
The Jackson Laboratory