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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Axin1Fu-ki
kinky
MGI:1856036
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Axin1Fu-ki/Axin1Fu-ki involves: Bagg albino * CF * fancier's mice MGI:3795122
hm2
Axin1Fu-ki/Axin1Fu-ki involves: BTBR MGI:3663637
hm3
Axin1Fu-ki/Axin1Fu-ki mixed MGI:3663590
ht4
Axin1Fu-ki/Axin1+ mixed MGI:3663589
ht5
Axin1Fu-ki/Axin1Fu-Tg1 involves: BTBR * C57BL/6J * CBA/J MGI:3663641


Genotype
MGI:3795122
hm1
Allelic
Composition
Axin1Fu-ki/Axin1Fu-ki
Genetic
Background
involves: Bagg albino * CF * fancier's mice
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Axin1Fu-ki mutation (0 available); any Axin1 mutation (44 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• most homozygotes are still alive at embryonic day 9, but the majority are dead by day 10 and all are dead by day 12

embryo
• instances are found of complete or partial duplication of the entire embryonic axis, or of individual organs such as the heart, or extraneous growth of a lump of tissue, or doubled neural folds
• seen in day 8 embryos
• 8 day embryos can have hyperplasia of neuroectoderm and mesenchyme yielding folds protruding into the amniotic cavity, 9 day embryos frequently have more contorted headfolds and neural folds
• 9 day embryos have abnormally small tail buds
• 8 and 9 day embryos frequently have abnormal embryonic membranes and some embryos are found outside of the yolk sac
• instances of multiple allantoides are found

growth/size/body
• seen in day 8 embryos

limbs/digits/tail
• 9 day embryos have abnormally small tail buds




Genotype
MGI:3663637
hm2
Allelic
Composition
Axin1Fu-ki/Axin1Fu-ki
Genetic
Background
involves: BTBR
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Axin1Fu-ki mutation (0 available); any Axin1 mutation (44 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system

embryo




Genotype
MGI:3663590
hm3
Allelic
Composition
Axin1Fu-ki/Axin1Fu-ki
Genetic
Background
mixed
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Axin1Fu-ki mutation (0 available); any Axin1 mutation (44 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging




Genotype
MGI:3663589
ht4
Allelic
Composition
Axin1Fu-ki/Axin1+
Genetic
Background
mixed
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Axin1Fu-ki mutation (0 available); any Axin1 mutation (44 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
• some vertebrae show abnormalities in structure, with one side shorter than the other, causing the following vertebra to form an angle with it
• two neighboring vertebrae may be fused, producing stiff tail segments
• may be reduced to as little as 1/2 of normal length
• occasionally observe bifurcations of the tail
• variable tail flexure, ranging from a barely perceptible bend or bump to a strong spiral twist

skeleton
• partial and total rib fusions due to reductions of vertebrae
• some vertebrae show abnormalities in structure, with one side shorter than the other, causing the following vertebra to form an angle with it
• two neighboring vertebrae may be fused, producing stiff tail segments
• abnormalities include eccentric reductions of single vertebrae
• ankyloses between adjacent vertebrae
• abnormalities include eccentric reductions of single vertebrae
• ankyloses between adjacent vertebrae
• abnormalities include eccentric reductions of single vertebrae
• ankyloses between adjacent vertebrae




Genotype
MGI:3663641
ht5
Allelic
Composition
Axin1Fu-ki/Axin1Fu-Tg1
Genetic
Background
involves: BTBR * C57BL/6J * CBA/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Axin1Fu-ki mutation (0 available); any Axin1 mutation (44 available)
Axin1Fu-Tg1 mutation (1 available); any Axin1 mutation (44 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• expanded pericardium

embryo
• E9.5 embryos exhibit poorly formed head folds and/or large globular mass attached to the head folds

growth/size/body
• E9.5 embryos exhibit a flattened head

craniofacial
• E9.5 embryos exhibit a flattened head





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