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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Hmx3tm1Tlu
targeted mutation 1, Tom Lufkin
MGI:1857577
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Hmx3tm1Tlu/Hmx3tm1Tlu involves: 129 * C57BL/6J MGI:2177662


Genotype
MGI:2177662
hm1
Allelic
Composition
Hmx3tm1Tlu/Hmx3tm1Tlu
Genetic
Background
involves: 129 * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hmx3tm1Tlu mutation (0 available); any Hmx3 mutation (15 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• intermating of heterozygotes results in only 70% of the expected number of homozygotes at 3 weeks
• intermating of homozygous mutant males with female heterozygotes results in 60% of the expected number of homozygotes at 3 weeks
• however, no embryonic loss of homozygotes is noted prior to birth (E10.5 to E18.5)

behavior/neurological
• by 2 weeks, 15% of homozygotes on a mixed genetic background display hyperactivity
• by 2 weeks, 15% of homozygotes on a mixed genetic background display hyperactive circling, with variable severity among individuals
• severely affected homozygotes circle at rates up to 176 rpm for several minutes, interspersed with non-circling periods of feeding, grooming and sleep
• Background Sensitivity: on a coisogenic 129/Sv background, 91% of homozygotes display circling vs 15% of homozygotes on a mixed 129/Sv x C57BL/6J background

hearing/vestibular/ear
• the horizontal (lateral) semicircular canal lacks both a horizontal crista and the associated horizontal ampullary chamber
• in contrast, the anterior and posterior cristae are completely normal
• adult homozygotes exhibit a complete loss of the horizontal semicircular canal crista
• adult homozygotes display abnormalities in vestibular sensory organ development
• however, both the sensory and secretory epithelium of the cochlear duct appear normal and hearing ability is apparently unaffected
• adult homozygotes display a fusion of the utricle and saccule endolymphatic spaces and depletion of sensory cells in these otolith organs
• adult homozygotes display a fusion of the utricle and saccule endolymphatic spaces into a common utriculosaccular chamber with a contiguous endolymphatic space
• adult homozygotes display a 35% loss in the sensory epithelial area of utricular macula
• however, no differences in otoconia or sensory hair bundles of the macula are observed
• adult homozygotes display a fusion of the utricle and saccule endolymphatic spaces into a common utriculosaccular chamber with a contiguous endolymphatic space
• adult homozygotes display a 15% loss in the sensory epithelial area of saccular macula
• however, no differences in otoconia or sensory hair bundles of the macula are observed

reproductive system
• at E4.5-E5.5, embryos remain unattached and fail to initiate any decidualization reaction
• female homozygotes produce normal oocytes, can be fertilized and their embryos undergo normal preimplantation development, but embryos fail to implant successfully in mutant uteri and subsequently die
• uterine histology is apparently normal, with no gross changes in the luminal epithelium, stroma or epithelial glands
• at postimplantation stage E5.5, unimplanted nercotic embryos are recovered from uteri of female homozygotes while, at later stages, 89% of females show no signs of embryo implantation
• transfer of preimplantation embryos from mutant uterine horns to wild-type pseudopregnant females results in successful pregnancy and birth
• 88% of female homozygotes exhibit reduced post-implantation fertility, with failure of a successful pregnancy despite repeated independent vaginal pluggings from wild-type males
• in contrast, male homozygotes are fertile

embryo
• at E4.5-E5.5, embryos remain unattached and fail to initiate any decidualization reaction





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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory