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Phenotypes Associated with This Genotype
Genotype
MGI:3044674
Allelic
Composition
Hip1tm1Tsr/Hip1tm1Tsr
Genetic
Background
involves: 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Hip1tm1Tsr mutation (0 available); any Hip1 mutation (67 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• fewer homozygotes generated from heterozygous intercrosses are found at weaning (22% vs expected 25%)
• however, normal Mendelian ratios and normal-appearing mutant embryos are detected from E12.5 to E18.5

reproductive system
• male homozygotes show reduced numbers of spermatogenic precursors at various stages of development relative to wild-type males
• at 6 weeks of age, mutant seminiferous tubules display consistently larger numbers of multinucleated giant cells than wild-type tubules
• at 6 weeks of age, male homozygotes display greater numbers of TUNEL-positive (apoptotic) postmeiotic spermatids than wild-type or heterozygous mice
• however, no consistent reduction is noted in the number of spermatogonial progenitors, as detected by GCNA staining
• at 6 weeks of age, male homozygotes show reduced eosinophilic material in the lumen of seminiferous tubules, indicating decreased numbers of mature sperm
• at 6 weeks of age, mutant seminiferous tubules display consistently larger numbers of multinucleated giant cells than wild-type tubules
• male homozygotes exhibit significantly higher histopathologic scores for testicular degeneration at all ages examined (6-, 7, 8-, and 20 weeks of age)
• the nuclei present in giant cells appear to be derived from spermatids at various stages of maturation
• at 6 to 7 weeks of age, male homozygotes exhibit significantly lower testicular weights than age-matched wild-type control males
• however, no differences in testicular weights are noted at 8-, 20- and 24 weeks of age, despite high histopathologic scores
• homozygotes display testicular atrophy associated with increased apoptosis of germ cells
• although germ cell development is clearly impaired, mutant sperm counts are sufficient to maintain fertility
• at 6 weeks of age, male homozygotes display fewer mature sperm in the epidiymides than wild-type males
• however, normal testicular weights and sperm counts are detected at >6 weeks of age

endocrine/exocrine glands
• at 6 weeks of age, male homozygotes show reduced eosinophilic material in the lumen of seminiferous tubules, indicating decreased numbers of mature sperm
• at 6 weeks of age, mutant seminiferous tubules display consistently larger numbers of multinucleated giant cells than wild-type tubules
• male homozygotes exhibit significantly higher histopathologic scores for testicular degeneration at all ages examined (6-, 7, 8-, and 20 weeks of age)
• the nuclei present in giant cells appear to be derived from spermatids at various stages of maturation
• at 6 to 7 weeks of age, male homozygotes exhibit significantly lower testicular weights than age-matched wild-type control males
• however, no differences in testicular weights are noted at 8-, 20- and 24 weeks of age, despite high histopathologic scores
• homozygotes display testicular atrophy associated with increased apoptosis of germ cells

hematopoietic system
N
• homozygotes display normal peripheral blood counts and a normal frequency of lymphoid progenitors relative to wild-type controls
• frequency of early progenitor (CFU-GEMM) colonies is severely reduced in 50% of homozygotes and normal in the remaining 50%
• however, frequency of clonogenic hematopoietic progenitors, BFU-E, and CFU-GM, is normal

vision/eye
N
• homozygotes do not exhibit microphthalmia

homeostasis/metabolism
N
• male homozygotes display no significant differences in serum FSH, LH, or prolactin levels relative to wild-type controls
• in addition, seminal vesicle weights, which are used as surrogate markers for serum testosterone, remain unaffected

behavior/neurological
N
• homozygotes do not develop any overt neurologic symptoms in the first year of life

cellular
• male homozygotes show reduced numbers of spermatogenic precursors at various stages of development relative to wild-type males
• at 6 weeks of age, male homozygotes display fewer mature sperm in the epidiymides than wild-type males
• however, normal testicular weights and sperm counts are detected at >6 weeks of age
• at 6 weeks of age, mutant seminiferous tubules display consistently larger numbers of multinucleated giant cells than wild-type tubules
• at 6 weeks of age, male homozygotes display greater numbers of TUNEL-positive (apoptotic) postmeiotic spermatids than wild-type or heterozygous mice
• however, no consistent reduction is noted in the number of spermatogonial progenitors, as detected by GCNA staining


Contributing Projects:
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
04/16/2024
MGI 6.23
The Jackson Laboratory