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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ing2tm1.1Ccha
targeted mutation 1.1, Curtis C Harri
MGI:4879096
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Ing2tm1.1Ccha/Ing2tm1.1Ccha involves: 129 * C57BL/6J * FVB/N MGI:4879097
cx2
Ing2tm1.1Ccha/Ing2tm1.1Ccha
Trp53tm1Brd/Trp53tm1Brd
involves: 129 * 129S7/SvEvBrd * C57BL/6J * FVB/N MGI:4879099


Genotype
MGI:4879097
hm1
Allelic
Composition
Ing2tm1.1Ccha/Ing2tm1.1Ccha
Genetic
Background
involves: 129 * C57BL/6J * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ing2tm1.1Ccha mutation (0 available); any Ing2 mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Testicular atrophy and semen abnormalities in Ing2tm1.1Ccha/Ing2tm1.1Ccha mice

mortality/aging
• recovered at a frequency (17%) less than the expected Mendelian ratio
• no lethality date was provided

reproductive system
• abnormal morphologies in spermatozoa, such as round heads, short tails, large heads, multiple tails and tail coiling
• spermatogonia are present in low numbers in seminiferous tubules
• hypospermia and degenerated round cells in epididymis at 8 weeks old
• aspermic epididymis at 24 months
• reduced number of normal sperm (~2%) at 8 weeks old
• become more severe with aging
• spermatogenesis arrest at meiotic phase in most tubules
• reduced 1N fractions (representing round and elongated spermatids) at 2 months of age, which were almost absent at 6 months
• relative increase in 2N fractions (spermatogonia and somatic cells)
• apparent loss of 4N fractions (spermatocytes) at 6 months
• defective in progression to the gamma-H2AX-negative pachytene stage
• severely impaired sperm motility
• decrease in acinar dilation in prostate
• seminiferous tubule degeneration, germ cell under-population with Leydig cell hyperplasia, apoptotic cells and multinucleated giant cells (spermatocytes) at 8 weeks old
• in some tubules various developmental stages can be seen up to round spermatid
• the major cell stage observed in these tubules is spermatocyte with large dense nuclei
• postmeiotic cell types such as round and elongated spermatids are scarcely observed
• most tubules remained devoid of germ cells and/or disorganized by 6 to 8 weeks
• progressive degeneration and germ cell depletion, eventually showing a Sertoli-cell-only pathology at 24 months
• smaller testis
• reduced testis weight starting from 4 weeks old
• normal body weight
• normal serum testosterone levels
• no gross abnormalities in other organs, including seminal vesicles, epididymides and vasa deferens
• infertile in males

cellular
• abnormal morphologies in spermatozoa, such as round heads, short tails, large heads, multiple tails and tail coiling
• spermatogonia are present in low numbers in seminiferous tubules
• hypospermia and degenerated round cells in epididymis at 8 weeks old
• aspermic epididymis at 24 months
• reduced number of normal sperm (~2%) at 8 weeks old
• become more severe with aging
• accumulated spermatocytes with the three acetylation sites on core histones (H3K18, H4K8 and H4K12) sites highly acetylated
• relative increase in 2N fractions (spermatogonia and somatic cells)
• spermatogenesis arrest at meiotic phase in most tubules
• reduced 1N fractions (representing round and elongated spermatids) at 2 months of age, which were almost absent at 6 months
• apparent loss of 4N fractions (spermatocytes) at 6 months
• defective in progression to the gamma-H2AX-negative pachytene stage
• increased numbers of TUNEL positive tubules and TUNEL-positive cells per tubule
• frequently in spermatocytes in luminal regions of the tubules
• severely impaired sperm motility

neoplasm
• increases in benign Harderian gland adenomas
• increased incidence of soft tissue sarcomas at time of death
• increased incidence preferentially in males

hematopoietic system
• increases in atypical lymphoid hyperplasia of the spleen

endocrine/exocrine glands
• decrease in acinar dilation in prostate
• increases in benign Harderian gland adenomas
• seminiferous tubule degeneration, germ cell under-population with Leydig cell hyperplasia, apoptotic cells and multinucleated giant cells (spermatocytes) at 8 weeks old
• in some tubules various developmental stages can be seen up to round spermatid
• the major cell stage observed in these tubules is spermatocyte with large dense nuclei
• postmeiotic cell types such as round and elongated spermatids are scarcely observed
• most tubules remained devoid of germ cells and/or disorganized by 6 to 8 weeks
• progressive degeneration and germ cell depletion, eventually showing a Sertoli-cell-only pathology at 24 months
• smaller testis
• reduced testis weight starting from 4 weeks old
• normal body weight
• normal serum testosterone levels
• no gross abnormalities in other organs, including seminal vesicles, epididymides and vasa deferens

immune system
• increases in atypical lymphoid hyperplasia of the spleen

growth/size/body
• increases in atypical lymphoid hyperplasia of the spleen




Genotype
MGI:4879099
cx2
Allelic
Composition
Ing2tm1.1Ccha/Ing2tm1.1Ccha
Trp53tm1Brd/Trp53tm1Brd
Genetic
Background
involves: 129 * 129S7/SvEvBrd * C57BL/6J * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ing2tm1.1Ccha mutation (0 available); any Ing2 mutation (16 available)
Trp53tm1Brd mutation (5 available); any Trp53 mutation (240 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Ing2tm1.1Ccha/Ing2tm1.1Ccha and Trp53tm1Brd/Trp53tm1Brd Ing2tm1.1Ccha/Ing2tm1.1Ccha mice exhibit increased testicular apoptosis and decreased testis weight

reproductive system
• hypospermia in epididymides
• reduced numbers of normal spermatozoa in semen
• degenerated large, round cells were accumulated in epididymis and semen
• less severe than those in Ing2tm1.1Ccha homozygous males
• degeneration of seminiferous tubules
• enhanced apoptosis
• reduced testis weight
• less severe than those in Ing2tm1.1Ccha homozygous males
• infertile in males

cellular
• hypospermia in epididymides
• reduced numbers of normal spermatozoa in semen
• degenerated large, round cells were accumulated in epididymis and semen
• less severe than those in Ing2tm1.1Ccha homozygous males
• increased numbers of TUNEL positive tubules and TUNEL-positive cells per tubule
• less severe than those in Ing2tm1.1Ccha homozygous males

endocrine/exocrine glands
• degeneration of seminiferous tubules
• enhanced apoptosis
• reduced testis weight
• less severe than those in Ing2tm1.1Ccha homozygous males





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
11/12/2024
MGI 6.24
The Jackson Laboratory