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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Atp7btx
toxic milk
MGI:1856220
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Atp7btx/Atp7btx DL-Atp7btx MGI:3793277
hm2
Atp7btx/Atp7btx involves: C57BL/6 * DL MGI:3793278


Genotype
MGI:3793277
hm1
Allelic
Composition
Atp7btx/Atp7btx
Genetic
Background
DL-Atp7btx
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Atp7btx mutation (1 available); any Atp7b mutation (82 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• pups suckled by homozygous mothers are deficient in copper concentration in their stomach contents and liver, and supplementing the drinking water of the homozygous mother with copper does not increase the copper content of the milk but rather increases the copper accumulation in the mammary gland

mortality/aging
• mice die at about 14 days of age
• severity of defects depends on genetic background (less severe on a mixes C57BL/6 background) and maternal age (decreasing severity with increasing maternal age)
• however, fostering with wild-type dams reverses many defects depending on the age of onset of fostering

reproductive system
• older female mice exhibit decreased fertility compared to wild-type mice

homeostasis/metabolism
• mice exhibit an increase copper accumulation in the kidney, spleen, brain, muscle, serum and red blood cells
• in postnatal mice
• in adult mice (J:7102)
• mice exhibit an increased concentration of zinc in the brain, liver and muscle

liver/biliary system
• in postnatal mice
• in adult mice (J:7102)

behavior/neurological
• mice exhibit tremors
• severity of defects depends on genetic background (less severe on a mixes C57BL/6 background) and maternal age (decreasing severity with increasing maternal age)
• however, fostering with wild-type dams reverses many defects depending on the age of onset of fostering
• mice exhibit difficulty walking, listing from side to side, overbalancing, falling over and exerting great effort in righting themselves
• severity of defects depends on genetic background (less severe on a mixes C57BL/6 background) and maternal age (decreasing severity with increasing maternal age)
• however, fostering with wild-type dams reverses many defects depending on the age of onset of fostering

growth/size/body
• mice reach their maximal weight at day 9 (70% of wild-type) and exhibit weight loss until their death
• severity of defects depends on genetic background (less severe on a mixes C57BL/6 background) and maternal age (decreasing severity with increasing maternal age)
• however, fostering with wild-type dams reverses many defects depending on the age of onset of fostering
• apparent within a day or two after birth
• severity of defects depends on genetic background (less severe on a mixes C57BL/6 background) and maternal age (decreasing severity with increasing maternal age)
• however, fostering with wild-type dams reverses many defects depending on the age of onset of fostering

muscle
• mice exhibit hyperextension of hindlimbs and hyperflexion of wrists
• severity of defects depends on genetic background (less severe on a mixes C57BL/6 background) and maternal age (decreasing severity with increasing maternal age)
• however, fostering with wild-type dams reverses many defects depending on the age of onset of fostering

pigmentation
• mice exhibit pale coat color
• severity of defects depends on genetic background (less severe on a mixes C57BL/6 background) and maternal age (decreasing severity with increasing maternal age)
• pigment contained within melanocytes is lighter than normal
• severity of defects depends on genetic background (less severe on a mixes C57BL/6 background) and maternal age (decreasing severity with increasing maternal age)
• however, fostering with wild-type dams reverses many defects depending on the age of onset of fostering

endocrine/exocrine glands
N
• mammary glands are structurally normal by histology

integument
• mice exhibit pale coat color
• severity of defects depends on genetic background (less severe on a mixes C57BL/6 background) and maternal age (decreasing severity with increasing maternal age)
• especially as mice approaches the end of its life expectancy at 2 weeks of age
• severity of defects depends on genetic background (less severe on a mixes C57BL/6 background) and maternal age (decreasing severity with increasing maternal age)
• however, fostering with wild-type dams reverses many defects depending on the age of onset of fostering
• mice exhibit curly whiskers
• severity of defects depends on genetic background (less severe on a mixes C57BL/6 background) and maternal age (decreasing severity with increasing maternal age)
• however, fostering with wild-type dams reverses many defects depending on the age of onset of fostering

nervous system

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Wilson disease DOID:893 OMIM:277900
J:35781




Genotype
MGI:3793278
hm2
Allelic
Composition
Atp7btx/Atp7btx
Genetic
Background
involves: C57BL/6 * DL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Atp7btx mutation (1 available); any Atp7b mutation (82 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• Background Sensitivity: mice exhibit less severe defects of those observed in mice on an inbred DL background

reproductive system
• Background Sensitivity: mice exhibit less severe defects of those observed in mice on an inbred DL background

homeostasis/metabolism
• Background Sensitivity: mice exhibit less severe defects of those observed in mice on an inbred DL background
• Background Sensitivity: mice exhibit less severe defects of those observed in mice on an inbred DL background
• Background Sensitivity: mice exhibit less severe defects of those observed in mice on an inbred DL background

liver/biliary system
• Background Sensitivity: mice exhibit less severe defects of those observed in mice on an inbred DL background
• Background Sensitivity: mice exhibit less severe defects of those observed in mice on an inbred DL background

behavior/neurological
• Background Sensitivity: mice exhibit less severe defects of those observed in mice on an inbred DL background
• Background Sensitivity: mice exhibit less severe defects of those observed in mice on an inbred DL background

growth/size/body
• Background Sensitivity: mice exhibit less severe defects of those observed in mice on an inbred DL background
• Background Sensitivity: mice exhibit less severe defects of those observed in mice on an inbred DL background

muscle
• Background Sensitivity: mice exhibit less severe defects of those observed in mice on an inbred DL background

pigmentation
• Background Sensitivity: mice exhibit less severe defects of those observed in mice on an inbred DL background
• Background Sensitivity: mice exhibit less severe defects of those observed in mice on an inbred DL background

integument
• Background Sensitivity: mice exhibit less severe defects of those observed in mice on an inbred DL background
• Background Sensitivity: mice exhibit less severe defects of those observed in mice on an inbred DL background
• Background Sensitivity: mice exhibit less severe defects of those observed in mice on an inbred DL background





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory