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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tbx3tm1Pa
targeted mutation 1, Virginia Papaioannou
MGI:2655214
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Tbx3tm1Pa/Tbx3tm1Pa either: (involves: 129 * 129S1/Sv * 129X1/SvJ) or (involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6NTac) MGI:2655216
ht2
Tbx3tm1Pa/Tbx3+ either: (involves: 129 * 129S1/Sv * 129X1/SvJ) or (involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6NTac) MGI:2655217


Genotype
MGI:2655216
hm1
Allelic
Composition
Tbx3tm1Pa/Tbx3tm1Pa
Genetic
Background
either: (involves: 129 * 129S1/Sv * 129X1/SvJ) or (involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6NTac)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tbx3tm1Pa mutation (1 available); any Tbx3 mutation (49 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• about 50% of homozygotes (17/35) die by E11.5; most homozygotes are dead by E12.5 (21/33)
• very few homozygotes survive beyond E13.5, rare exceptions (2/35) survive to about E16.5

embryo
• 6 of 24 homozygotes show a reduction in yolk sac vasculature prior to E10.5
• 6 of 24 homozygotes exhibit small or absent yolk sac blood vessels prior to E10.5
• at E10.5, homozygotes exhibit a thinner and anteroposteriorly less extensive AER in the forelimbs, and a severely reduced AER in the hindlimbs
• ~70% of homozygotes display reduced hindlimb bud development by E9.5-E10.5
• however, no major abnormalities are detected at E8.5
• by E12.5, yolk sacs of many surviving homozygotes display an abnormal endoderm layer composed of mostly dead cells with pyknotic nuclei and deteriorating blood vessels
• 6 of 24 mutant yolk sacs contain no blood, although blood is present in the heart and embryonic circulation

limbs/digits/tail
• only digit one forms in homozygous mutant hindlimbs
• by E11.5, all homozygotes exhibit forelimb abnormalities
• one fetus surviving to ~E16.5, exhibits a right forelimb with a shortened ulna and a left forelimb without an ulna
• by E11.5, all homozygotes exhibit hindlimb abnormalities
• hindlimbs are always the more severely affected than forelimbs
• one fetus surviving to ~E16.5, exhibits a right forelimb with absent metacarpals and phalanges of the fifth digit, and absent phalanges of the fourth digiit; the left forelimb lacks an ulna and carpals as well as metacarpals and phalanges of the fourth and fifth digits
• at E10.5, homozygotes exhibit a thinner and anteroposteriorly less extensive AER in the forelimbs, and a severely reduced AER in the hindlimbs
• ~70% of homozygotes display reduced hindlimb bud development by E9.5-E10.5
• however, no major abnormalities are detected at E8.5
• by E11.5, homozygotes display irregularities in the hand plate and either little development or an aberrant shape to the foot plate that resembles a posterior deflection of the autopod

liver/biliary system
• at E12.5, homozygotes exhibit a smaller liver relative to wild-type embryos

endocrine/exocrine glands
• homozygotes display failure of mammary bud induction at E12.5-E13.5
• homozygotes exhibit absence or reduction of mammary buds between E11.5 and E13.5
• no mammary buds are detected at E12.5, although at E13.5 one of seven mutants displayed a single, small pair of mammary buds at the level corresponding to bud number 2, and a second mutant had a single, unilateral bud in a similar position; however, these appeared less organized relative to wild-type mammary buds

skeleton
• one fetus surviving to ~E16.5, exhibits a right forelimb with a shortened ulna and a left forelimb without an ulna
• one fetus surviving to ~E16.5, exhibits a right forelimb with absent metacarpals and phalanges of the fifth digit, and absent phalanges of the fourth digiit; the left forelimb lacks an ulna and carpals as well as metacarpals and phalanges of the fourth and fifth digits
• rare homozygous fetuses that survive to E16.5 (2/35), display small, malformed pelvic bones

cardiovascular system
• 6 of 24 homozygotes show a reduction in yolk sac vasculature prior to E10.5
• 6 of 24 homozygotes exhibit small or absent yolk sac blood vessels prior to E10.5

integument
• homozygotes display failure of mammary bud induction at E12.5-E13.5
• homozygotes exhibit absence or reduction of mammary buds between E11.5 and E13.5
• no mammary buds are detected at E12.5, although at E13.5 one of seven mutants displayed a single, small pair of mammary buds at the level corresponding to bud number 2, and a second mutant had a single, unilateral bud in a similar position; however, these appeared less organized relative to wild-type mammary buds

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
ulnar-mammary syndrome DOID:0060614 OMIM:181450
J:82458




Genotype
MGI:2655217
ht2
Allelic
Composition
Tbx3tm1Pa/Tbx3+
Genetic
Background
either: (involves: 129 * 129S1/Sv * 129X1/SvJ) or (involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6NTac)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tbx3tm1Pa mutation (1 available); any Tbx3 mutation (49 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• all adult heterozyotes exhibit a small ventral split in the glans clitoris, resulting in a distal bifurcation of the prepuce
• 9 of 85 adult heterozygotes display a failure of vaginal opening





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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
04/23/2024
MGI 6.23
The Jackson Laboratory