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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Fst+
wild type
MGI:2439776
Summary 8 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Fsttm1Zuk/Fst+ B6.129S7-Fsttm1Zuk MGI:5319775
ht2
Fstem1(IMPC)Wtsi/Fst+ C57BL/6NCrl-Fstem1(IMPC)Wtsi/Wtsi MGI:7629001
ht3
Fsttm1Zuk/Fst+ involves: 129S7/SvEvBrd MGI:3814734
ht4
Fsttm1Zuk/Fst+ involves: 129S7/SvEvBrd * C57BL/6 MGI:3814735
cx5
Fsttm1Zuk/Fst+
Fstl3tm1.1Sjl/Fstl3tm1.1Sjl
B6.129-Fsttm1Zuk Fstl3tm1.1Sjl MGI:5319774
cx6
Fsttm1Zuk/Fst+
Mstntm1Sjl/Mstntm1Sjl
B6.129-Mstntm1Sjl Fsttm1Zuk MGI:5319776
cx7
Fsttm1Zuk/Fst+
Mstntm1Sjl/Mstn+
B6.129-Mstntm1Sjl Fsttm1Zuk MGI:5319777
cx8
Fsttm1Zuk/Fst+
Wfikkn1tm1.1Sjl/Wfikkn1tm1.1Sjl
involves: 129S7/SvEvBrd * C57BL/6 MGI:5546337


Genotype
MGI:5319775
ht1
Allelic
Composition
Fsttm1Zuk/Fst+
Genetic
Background
B6.129S7-Fsttm1Zuk
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fsttm1Zuk mutation (2 available); any Fst mutation (19 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
muscle
• increase in the percentage of oxidative type I fibers
• increase in the number of oxidative type I fibers
• increase in the proportion of smaller fibers that stain more darkly in hematoxylin and eosin stained sections corresponding to mixed glycolytic/oxidative type IIa fibers
• shift towards more oxidative fibers
• decrease in mean fiber diameter for each fiber type
• about 15-20% lower than wild-type
• decreased triceps weight
• lower twitch and tetanic force production
• but no change in specific force

homeostasis/metabolism
• impaired muscle regeneration and enhanced fibrosis in the gastrocnemius muscle following cardiotoxin-induced injury

limbs/digits/tail
• increase in the percentage of oxidative type I fibers
• increase in the number of oxidative type I fibers




Genotype
MGI:7629001
ht2
Allelic
Composition
Fstem1(IMPC)Wtsi/Fst+
Genetic
Background
C57BL/6NCrl-Fstem1(IMPC)Wtsi/Wtsi
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fstem1(IMPC)Wtsi mutation (1 available); any Fst mutation (19 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype
adipose tissue

growth/size/body

skeleton

vision/eye




Genotype
MGI:3814734
ht3
Allelic
Composition
Fsttm1Zuk/Fst+
Genetic
Background
involves: 129S7/SvEvBrd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fsttm1Zuk mutation (2 available); any Fst mutation (19 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• in 26.6% (4 of 15) heterozygotes, development of the thirteenth pair of ribs is limited; not oberved in wild-type controls
• Background Sensitivity: a higher percentage of heterozygotes show limited formation of the thirteenth rib pair on an inbred 129/SvEv background than on a hybrid 129/SvEv x C57BL/6 background (26.6% vs 17%, respectively)
• 86.6% (13 of 15) heterozygotes have five lumbar vertebrae instead of six found in wild-type controls
• Background Sensitivity: a higher percentage of heterozygotes show five lumbar vertebrae on an inbred 129/SvEv background than on a hybrid 129/SvEv x C57BL/6 background (86.6% vs 60%, respectively)




Genotype
MGI:3814735
ht4
Allelic
Composition
Fsttm1Zuk/Fst+
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fsttm1Zuk mutation (2 available); any Fst mutation (19 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• in 17% (6 of 35) heterozygotes, development of the thirteenth pair of ribs is limited; not oberved in wild-type controls
• Background Sensitivity: a higher percentage of heterozygotes show limited formation of the thirteenth rib pair on an inbred 129/SvEv background than on a hybrid 129/SvEv x C57BL/6 background (26.6% vs 17%, respectively)
• 60% (21 of 35) heterozygotes have five lumbar vertebrae instead of six; only 2 of 15 wild-type controls show this defect
• Background Sensitivity: a higher percentage of heterozygotes show five lumbar vertebrae on an inbred 129/SvEv background than on a hybrid 129/SvEv x C57BL/6 background (86.6% vs 60%, respectively)




Genotype
MGI:5319774
cx5
Allelic
Composition
Fsttm1Zuk/Fst+
Fstl3tm1.1Sjl/Fstl3tm1.1Sjl
Genetic
Background
B6.129-Fsttm1Zuk Fstl3tm1.1Sjl
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fstl3tm1.1Sjl mutation (0 available); any Fstl3 mutation (20 available)
Fsttm1Zuk mutation (2 available); any Fst mutation (19 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
muscle
• similar to mice heterozygous for Fsttm1Zuk alone




Genotype
MGI:5319776
cx6
Allelic
Composition
Fsttm1Zuk/Fst+
Mstntm1Sjl/Mstntm1Sjl
Genetic
Background
B6.129-Mstntm1Sjl Fsttm1Zuk
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fsttm1Zuk mutation (2 available); any Fst mutation (19 available)
Mstntm1Sjl mutation (2 available); any Mstn mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
muscle
• relative to mice homoozygous for Mstntm1Sjl alone




Genotype
MGI:5319777
cx7
Allelic
Composition
Fsttm1Zuk/Fst+
Mstntm1Sjl/Mstn+
Genetic
Background
B6.129-Mstntm1Sjl Fsttm1Zuk
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fsttm1Zuk mutation (2 available); any Fst mutation (19 available)
Mstntm1Sjl mutation (2 available); any Mstn mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
muscle
• relative to mice heterozygous for Mstntm1Sjl alone

growth/size/body
• relative to mice heterozygous for Mstntm1Sjl alone




Genotype
MGI:5546337
cx8
Allelic
Composition
Fsttm1Zuk/Fst+
Wfikkn1tm1.1Sjl/Wfikkn1tm1.1Sjl
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fsttm1Zuk mutation (2 available); any Fst mutation (19 available)
Wfikkn1tm1.1Sjl mutation (0 available); any Wfikkn1 mutation (13 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Axial skeleton patterning defects in Wfikkn1tm1.1Sjl/Wfikkn1tm1.1Sjl, Wfikkn1tm1.1Sjl/Wfikkn1tm1.1Sjl Fsttm1Zuk/Fsttm1Zuk, Gdf11tm1Sjl/Gdf11+ and Gdf11tm1Sjl/Gdf11tm1Sjl mice.

skeleton
• cervical ribs are seen on one or both sides in most mice
• over 90% of mice are missing both 13th ribs
• cervical ribs are seen on one or both sides in most mice
• most mice have 12 thoracic vertebrae
• 25% of mice have 6/7 lumbar vertebrae





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last database update
03/25/2025
MGI 6.24
The Jackson Laboratory