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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
anx
anorexia
MGI:1856657
Summary 6 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
anx/anx B6C3Fe a/a-anx/J MGI:2653752
hm2
anx/anx involves: DW/J * M. m. domesticus poschiavinus * Swiss MGI:3828834
cx3
anx/anx
Tg(Tyro3*-Gfp)1Sapc/?
Tyro3m1/Tyro3m1
involves: C3HeB/FeJLe * C57BL/6J MGI:6287394
cx4
anx/anx
Tg(TYRO3)1Sapc/?
Tyro3m1/Tyro3m1
involves: C3HeB/FeJLe * C57BL/6J MGI:6287398
cx5
anx/anx
Tyro3m1/Tyro3m1
involves: C3HeB/FeJLe * C57BL/6J MGI:6284561
cx6
anx/anx
Tg(Tyro3-GFP)1Sapc/?
Tyro3m1/Tyro3m1
involves: C3HeB/FeJLe * C57BL/6J MGI:6287219


Genotype
MGI:2653752
hm1
Allelic
Composition
anx/anx
Genetic
Background
B6C3Fe a/a-anx/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
anx mutation (1 available); any anx mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mutant mice die in a state of anorexia and emaciation at ~P22

behavior/neurological
• failure to ingest sufficient amount of nutrients to sustain growth, indicating anorexia, starting at ~P5
• however, no deficiency in dietary or serum zinc (a frequent metabolic cause of anorexia) is observed
• physiological and behavioral phenotypes appear to result from a suckling dysfunction
• head and body tremors at P18 or later
• reduction in severity of head and body tremors following i.p. injection of the serotonin antagonist 5,7-dihydroxytryptamine at P20
• headweaving at P18 or later
• uncoordinated gait at P18 or later
• reduction in severity of abnormal gait following i.p. injection of the serotonin antagonist 5,7-dihydroxytryptamine at P20
• hyperactivity at P18 or later
• reduction in hyperactivity following i.p. injection of the serotonin antagonist 5,7-dihydroxytryptamine at P20

growth/size/body
• significant reduction in body weight at P9
• anorexic mutants are first recognized at ~P5 by a thinning of the neck and tail, and later by growth arrest and emaciation

immune system
• significant increase in thymus weight at P15 but not at P5
• beginning at ~P5, spleen size is reduced
• significant reduction in spleen weight both at P5 and at P15
• beginning at ~P5, spleen is pale in color
• however, total RBC count, hemoglobin, hematocrit, and mean corpuscular volume (MCV) are within normal range

homeostasis/metabolism
• significantly increased blood urea nitrogen levels relative to wild-type littermates at P15 (62.5 mg/dl vs 43.8 mg/dl, respectively)
• significantly increased blood uric acid levels relative to wild-type littermates at P15 (4.6 mg/dl vs 1.2 mg/dl, respectively)
• significantly decreased blood glucose levels relative to wild-type littermates at P15 (58 mg/dl vs 129 mg/dl, respectively)
• significantly increased serum cholesterol levels relative to wild-type littermates at P15 (1.92 0.18 mg/ml vs 1.12 0.04 mg/ml, respectively)
• significantly increased circulating alkaline phosphatase levels relative to wild-type littermates at P15 (1020 mU/ml vs 385 mU/ml, respectively)
• significant hypothermia at ~P22, but not at P5, P10 or P15

liver/biliary system
• at P15, livers display a lacey appearance and are devoid of fat and glycogen

nervous system
• at P15, brains display an abundance of capillaries
• significant increase in brain weight both at P5 and at P15

cardiovascular system
• at P15, brains display an abundance of capillaries

hematopoietic system
• significant increase in thymus weight at P15 but not at P5
• beginning at ~P5, spleen size is reduced
• significant reduction in spleen weight both at P5 and at P15
• beginning at ~P5, spleen is pale in color
• however, total RBC count, hemoglobin, hematocrit, and mean corpuscular volume (MCV) are within normal range

endocrine/exocrine glands
• significant increase in thymus weight at P15 but not at P5




Genotype
MGI:3828834
hm2
Allelic
Composition
anx/anx
Genetic
Background
involves: DW/J * M. m. domesticus poschiavinus * Swiss
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
anx mutation (1 available); any anx mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mutant mice die in a state of anorexia and emaciation at ~P22

behavior/neurological
• poor appetite starting at ~P5
• failure to ingest sufficient amount of nutrients to sustain growth, indicating anorexia
• head and body tremors
• uncoordinated gait

growth/size/body
• significant reduction in body weight
• emaciation by ~P22

digestive/alimentary system
• beginning at ~P5, stomach contents are reduced
• by ~P22 (time of death), stomach and intestines are devoid of food

hematopoietic system
• beginning at ~P5, spleen is pale in color
• however, hemoglobin, hematocrit, and mean corpuscular volume (MCV) are within normal range
• beginning at ~P5, spleen size is reduced

homeostasis/metabolism
• hypothermia at ~P22

liver/biliary system
• at P15, livers are devoid of fat and glycogen

nervous system
• at P15, brains display an abundance of capillaries, suggesting hyperemia

cardiovascular system
• at P15, brains display an abundance of capillaries, suggesting hyperemia

immune system
• beginning at ~P5, spleen is pale in color
• however, hemoglobin, hematocrit, and mean corpuscular volume (MCV) are within normal range
• beginning at ~P5, spleen size is reduced




Genotype
MGI:6287394
cx3
Allelic
Composition
anx/anx
Tg(Tyro3*-Gfp)1Sapc/?
Tyro3m1/Tyro3m1
Genetic
Background
involves: C3HeB/FeJLe * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
anx mutation (1 available); any anx mutation (1 available)
Tg(Tyro3*-Gfp)1Sapc mutation (0 available)
Tyro3m1 mutation (4 available); any Tyro3 mutation (40 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological

mortality/aging

growth/size/body
• unlike wildtype Tyro3, transgenic expression of this R7W point mutant transgene fails to resuce the anx homozygous phenotype, specifically cachexia, death by 21 days of age, and behavioral phenotypes such as head tossing and tremors




Genotype
MGI:6287398
cx4
Allelic
Composition
anx/anx
Tg(TYRO3)1Sapc/?
Tyro3m1/Tyro3m1
Genetic
Background
involves: C3HeB/FeJLe * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
anx mutation (1 available); any anx mutation (1 available)
Tg(TYRO3)1Sapc mutation (0 available)
Tyro3m1 mutation (4 available); any Tyro3 mutation (40 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• relative to anx homozygotes lacking the TYRO3 human wildtype transgene, these mice show a partial rescue of the anorexia phenotype with the body weight at 21 days of age 92.8% increased on average

mortality/aging
• wildtype human TYRO3 partially rescues the anx homozygous phenotype, with anx homozygotes still dying prematurely, but surviving past 35 days of age and showing no or only mild behavioural phentoypes of headweaving, ataxia, or tremors




Genotype
MGI:6284561
cx5
Allelic
Composition
anx/anx
Tyro3m1/Tyro3m1
Genetic
Background
involves: C3HeB/FeJLe * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
anx mutation (1 available); any anx mutation (1 available)
Tyro3m1 mutation (4 available); any Tyro3 mutation (40 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body

nervous system
• at 19 days of age only 20.2% of normal levels of Npy+ soma are present in the arcuate nucleus, the Npy+ cell bodies are clustered aberrantly within and adjacent to the median eminence, and lack Npy+ processes that normally extend towards and into the paraventricular nucleus or dorsomedial nucleus of the hypothalamus

hematopoietic system
• platelets from homozygotes appear smaller and 17.5% contain large vacuoles, although electron microscopy shows only normal morphology and numbers of dense and alpha granules
• after activation with thrombin, platelets from homozygotes have decreased levels of P-selectin on the surface compared with heterozgyous or wildtype controls

homeostasis/metabolism
• after activation with thrombin, platelets from homozygotes have decreased levels of P-selectin on the surface compared with heterozgyous or wildtype controls




Genotype
MGI:6287219
cx6
Allelic
Composition
anx/anx
Tg(Tyro3-GFP)1Sapc/?
Tyro3m1/Tyro3m1
Genetic
Background
involves: C3HeB/FeJLe * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
anx mutation (1 available); any anx mutation (1 available)
Tg(Tyro3-GFP)1Sapc mutation (0 available)
Tyro3m1 mutation (4 available); any Tyro3 mutation (40 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• relative to anx homozygotes lacking the Tyro3 wildtype transgene, these mice show a partial rescue of phenotype with the body weight at 21 days of age 83.5% increased on average

mortality/aging
• wildtype mouse Tyro3 partially rescues the anx homozygous phenotype, with anx homozygotes still dying prematurely, but surviving past 35 days of age, having 83.58% of Npy+ soma retained in and properly distributed in the arcuate nucleus at 19 days of age, and showing no or only mild behavioural phentoypes of headweaving, ataxia, or tremors





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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory