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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Inpp5btm1Nbm
targeted mutation 1, Robert L Nussbaum
MGI:2159609
Summary 7 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Inpp5btm1Nbm/Inpp5btm1Nbm 129/Sv-Inpp5btm1Nbm MGI:3040920
hm2
Inpp5btm1Nbm/Inpp5btm1Nbm either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * NIH Black Swiss) MGI:2668818
cx3
Inpp5btm1Nbm/Inpp5btm1Nbm
Ocrltm1Nbm/Ocrltm1Nbm
either: (involves: 129S/SvEv * 129S6/SvEvTac * C57BL/6) or (involves: 129S/SvEv * 129S6/SvEvTac * C57BL/6 * NIH Black Swiss) or (involves: 129S/SvEv * 129S6/SvEvTac * NIH Black Swiss) MGI:3040919
cx4
Inpp5btm1Nbm/Inpp5btm1Nbm
Ocrltm1Nbm/Y
Tg(INPP5B)CNbm/Tg(INPP5B)CNbm
involves: 129S/SvEv * 129S6/SvEvTac * FVB/N MGI:5430754
cx5
Inpp5btm1Nbm/Inpp5btm1Nbm
Ocrltm1Nbm/Ocrltm1Nbm
Tg(INPP5B)CNbm/0
involves: 129S/SvEv * 129S6/SvEvTac * FVB/N MGI:5430751
cx6
Inpp5btm1Nbm/Inpp5btm1Nbm
Ocrltm1Nbm/Y
Tg(INPP5B)CNbm/0
involves: 129S/SvEv * 129S6/SvEvTac * FVB/N MGI:5430752
cx7
Inpp5btm1Nbm/Inpp5btm1Nbm
Ocrltm1Nbm/Ocrltm1Nbm
Tg(INPP5B)CNbm/Tg(INPP5B)CNbm
involves: 129S/SvEv * 129S6/SvEvTac * FVB/N MGI:5430753


Genotype
MGI:3040920
hm1
Allelic
Composition
Inpp5btm1Nbm/Inpp5btm1Nbm
Genetic
Background
129/Sv-Inpp5btm1Nbm
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Inpp5btm1Nbm mutation (0 available); any Inpp5b mutation (57 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
• by P13 and more severely by P21 vacuoles containing adherens junctions are seen in the seminiferous tubules of mutant mice

reproductive system
• in swim up preparations sperm counts are reduced to about 5% of heterozygous controls
• only 61% of mutant sperm are motile compared to 85% in heterozygous controls
• those mutant sperm that are motile display reduced sperm velocity parameters
• by P13 and more severely by P21 vacuoles containing adherens junctions are seen in the seminiferous tubules of mutant mice
• at P13 spermatogenesis is disrupted at meiosis I and at P21 mutant testes show a loss of meiotic germ cells
• at 4 weeks excess round germ cells are seen in the cauda epididymis this is not seen at 6 months
• by 6 weeks testes in mutants begin to recover with germ cells and sperm evident
• between 2 and 6 months spermatogenesis appears normal, however by 1 year a severe disruption in spermatogenesis with a complete loss of spermatocytes and spermatids is seen
• total cauda epididymal sperm counts are reduced to 53% of heterozygous controls
• infertile males are unable to process Adam2
• only 1 male out of 17 sired any pups and that litter was smaller than normal
• even when swim-up preparations of sperm were used to concentrate motile mutant sperm, mutant sperm fertilize a significantly lower percentage of eggs compared to heterozygous controls

cellular
• total cauda epididymal sperm counts are reduced to 53% of heterozygous controls
• in swim up preparations sperm counts are reduced to about 5% of heterozygous controls
• only 61% of mutant sperm are motile compared to 85% in heterozygous controls
• those mutant sperm that are motile display reduced sperm velocity parameters




Genotype
MGI:2668818
hm2
Allelic
Composition
Inpp5btm1Nbm/Inpp5btm1Nbm
Genetic
Background
either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * NIH Black Swiss)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Inpp5btm1Nbm mutation (0 available); any Inpp5b mutation (57 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• young males are fertile however as males age progressive testicular degeneration results in sterility




Genotype
MGI:3040919
cx3
Allelic
Composition
Inpp5btm1Nbm/Inpp5btm1Nbm
Ocrltm1Nbm/Ocrltm1Nbm
Genetic
Background
either: (involves: 129S/SvEv * 129S6/SvEvTac * C57BL/6) or (involves: 129S/SvEv * 129S6/SvEvTac * C57BL/6 * NIH Black Swiss) or (involves: 129S/SvEv * 129S6/SvEvTac * NIH Black Swiss)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Inpp5btm1Nbm mutation (0 available); any Inpp5b mutation (57 available)
Ocrltm1Nbm mutation (1 available); any Ocrl mutation (9 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• at E9.5 no double homozygous embryos could be found




Genotype
MGI:5430754
cx4
Allelic
Composition
Inpp5btm1Nbm/Inpp5btm1Nbm
Ocrltm1Nbm/Y
Tg(INPP5B)CNbm/Tg(INPP5B)CNbm
Genetic
Background
involves: 129S/SvEv * 129S6/SvEvTac * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Inpp5btm1Nbm mutation (0 available); any Inpp5b mutation (57 available)
Ocrltm1Nbm mutation (1 available); any Ocrl mutation (9 available)
Tg(INPP5B)CNbm mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body

renal/urinary system
N
• mice do not exhibit low molecular weight proteinuria




Genotype
MGI:5430751
cx5
Allelic
Composition
Inpp5btm1Nbm/Inpp5btm1Nbm
Ocrltm1Nbm/Ocrltm1Nbm
Tg(INPP5B)CNbm/0
Genetic
Background
involves: 129S/SvEv * 129S6/SvEvTac * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Inpp5btm1Nbm mutation (0 available); any Inpp5b mutation (57 available)
Ocrltm1Nbm mutation (1 available); any Ocrl mutation (9 available)
Tg(INPP5B)CNbm mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• a few mice die by 6 weeks of age

growth/size/body
• in a few mice

renal/urinary system

vision/eye
N
• mice exhibit normal lens development and do not develop cataracts

homeostasis/metabolism




Genotype
MGI:5430752
cx6
Allelic
Composition
Inpp5btm1Nbm/Inpp5btm1Nbm
Ocrltm1Nbm/Y
Tg(INPP5B)CNbm/0
Genetic
Background
involves: 129S/SvEv * 129S6/SvEvTac * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Inpp5btm1Nbm mutation (0 available); any Inpp5b mutation (57 available)
Ocrltm1Nbm mutation (1 available); any Ocrl mutation (9 available)
Tg(INPP5B)CNbm mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• a few mice die by 6 weeks of age

growth/size/body
• in a few mice

renal/urinary system

vision/eye
N
• mice exhibit normal lens development and do not develop cataracts

homeostasis/metabolism




Genotype
MGI:5430753
cx7
Allelic
Composition
Inpp5btm1Nbm/Inpp5btm1Nbm
Ocrltm1Nbm/Ocrltm1Nbm
Tg(INPP5B)CNbm/Tg(INPP5B)CNbm
Genetic
Background
involves: 129S/SvEv * 129S6/SvEvTac * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Inpp5btm1Nbm mutation (0 available); any Inpp5b mutation (57 available)
Ocrltm1Nbm mutation (1 available); any Ocrl mutation (9 available)
Tg(INPP5B)CNbm mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body

renal/urinary system
N
• mice do not exhibit low molecular weight proteinuria





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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory