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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cdkn1btm1Kin
targeted mutation 1, Kei-ichi Nakayama
MGI:1888790
Summary 7 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cdkn1btm1Kin/Cdkn1btm1Kin involves: 129P2/OlaHsd * C57BL/6 MGI:2175760
cx2
Cdkn1btm1Kin/Cdkn1btm1Kin
Zfp949tm1Htno/Zfp949tm1Htno
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ MGI:6152408
cx3
Cdkn1btm1Kin/Cdkn1btm1Kin
Skp2tm1Kin/Skp2tm1Kin
involves: 129P2/OlaHsd * C57BL/6 MGI:3036549
cx4
Cdkn1btm1Kin/Cdkn1b+
Irs2tm1Mfw/Irs2tm1Mfw
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J MGI:3529771
cx5
Cdkn1btm1Kin/Cdkn1btm1Kin
Irs2tm1Mfw/Irs2tm1Mfw
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J MGI:3529769
cx6
Cdkn1btm1Kin/Cdkn1b+
Leprdb/Leprdb
involves: C57BL/6J * C57BLKS/J MGI:3529778
cx7
Cdkn1btm1Kin/Cdkn1btm1Kin
Leprdb/Leprdb
involves: C57BL/6J * C57BLKS/J MGI:3529774


Genotype
MGI:2175760
hm1
Allelic
Composition
Cdkn1btm1Kin/Cdkn1btm1Kin
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkn1btm1Kin mutation (1 available); any Cdkn1b mutation (25 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• about half of mutants develop tumors originating from the intermediate lobe by 12 weeks of age

pigmentation
• the pigment epithelium layer was thickened and cells composing it were taller than normal

endocrine/exocrine glands
• marked hyperplasia of the medulla however the cortex remained normal
• weight of pituitary was more than 2-fold that of wildtype
• intermediate lobes were hyperplastic while the anterior and posterior lobes were relatively normal
• thymus sometimes totally covered the heart
• elevated number of of thymocytes
• formation of corpus luteum was not seen at 12 weeks of age
• marked accumulation of atypical follicles with extensive hyperplasia of granulosa cells, whereas theca cells remained normal
• follicles contained fewer apoptotic cells and degenerative granulosa cells than in control atretic follicles
• atypical follicles with extensive hyperplasia of granulosa cells
• no evidence of Graafian follicles in ovaries
• most of the accumulated follicles were primary and secondary follicles, but further development was impaired
• formation of the cavity (antrum) was much less prominent than in controls
• ovary was 2-fold larger than in controls
• testis was 2-fold larger than in controls
• about half of mutants develop tumors originating from the intermediate lobe by 12 weeks of age

growth/size/body
• ovary was 2-fold larger than in controls
• weight of organs increased in proportion to the whole body weight, except for a few enlarged organs
• by 4-6 weeks of age, weigh more than controls with the weight difference becoming more pronounced with age, however did not gain weight faster than controls

hematopoietic system
• thymus sometimes totally covered the heart
• elevated number of of thymocytes
• some mutants contained 2-fold more T cells in the spleen and lymph notes, however number of B cells was normal

immune system
• thymus sometimes totally covered the heart
• elevated number of of thymocytes
• some mutants contained 2-fold more T cells in the spleen and lymph notes, however number of B cells was normal

reproductive system
• formation of corpus luteum was not seen at 12 weeks of age
• marked accumulation of atypical follicles with extensive hyperplasia of granulosa cells, whereas theca cells remained normal
• follicles contained fewer apoptotic cells and degenerative granulosa cells than in control atretic follicles
• atypical follicles with extensive hyperplasia of granulosa cells
• no evidence of Graafian follicles in ovaries
• most of the accumulated follicles were primary and secondary follicles, but further development was impaired
• formation of the cavity (antrum) was much less prominent than in controls
• ovary was 2-fold larger than in controls
• testis was 2-fold larger than in controls
• endometrium and interstitial tissue of the uterus were always hyperplastic
• endometrium of the uterus was always hyperplastic

vision/eye
• increase in Mullers supporting cells in the inner granular layer
• increase in amacrine cells in the inner granular layer
• partial loss of the rod and cone layer
• the pigment epithelium layer was thickened and cells composing it were taller than normal
• the outer granular layer invaded the layer of rods and cones beyond the outer limiting membrane
• the inner granular layer exhibited a displacement of bipolar cells, with an increase in the number of amacrine cells and Mullers supporting cells, and a disorganization of the network of cell fibers
• the outer limiting membrane was irregular and not clearly recognizable
• variable reduction in electroretinographic (ERG) amplitudes

nervous system
• weight of pituitary was more than 2-fold that of wildtype
• intermediate lobes were hyperplastic while the anterior and posterior lobes were relatively normal
• about half of mutants develop tumors originating from the intermediate lobe by 12 weeks of age
• increase in Mullers supporting cells in the inner granular layer
• increase in amacrine cells in the inner granular layer
• partial loss of the rod and cone layer




Genotype
MGI:6152408
cx2
Allelic
Composition
Cdkn1btm1Kin/Cdkn1btm1Kin
Zfp949tm1Htno/Zfp949tm1Htno
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkn1btm1Kin mutation (1 available); any Cdkn1b mutation (25 available)
Zfp949tm1Htno mutation (0 available); any Zfp949 mutation (37 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• fewer than expected mice are present at E9.5, E10.5 and E11.5
• no mice are recovered after E11.5

embryo
• some turning at E10.5

growth/size/body

cellular
• not as severe as in Zfp949tm1Htno homozygotes




Genotype
MGI:3036549
cx3
Allelic
Composition
Cdkn1btm1Kin/Cdkn1btm1Kin
Skp2tm1Kin/Skp2tm1Kin
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkn1btm1Kin mutation (1 available); any Cdkn1b mutation (25 available)
Skp2tm1Kin mutation (1 available); any Skp2 mutation (45 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
N
• cell proliferation in wound recovery is normal




Genotype
MGI:3529771
cx4
Allelic
Composition
Cdkn1btm1Kin/Cdkn1b+
Irs2tm1Mfw/Irs2tm1Mfw
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkn1btm1Kin mutation (1 available); any Cdkn1b mutation (25 available)
Irs2tm1Mfw mutation (1 available); any Irs2 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
• beta cell proliferation and the total number of beta cells are increased compared to Irs2 single homozygotes; however the size of individual beta cells is similar to Irs2 single homozygotes
• islet mass, but not islet density, is significantly increased compared to Irs2 single homozygotes

homeostasis/metabolism
• compound mutants have significantly elevated blood glucose levels at 18 weeks; however this elevation is slight compared to Irs2 single homozygotes
• fasting serum insulin levels are increased




Genotype
MGI:3529769
cx5
Allelic
Composition
Cdkn1btm1Kin/Cdkn1btm1Kin
Irs2tm1Mfw/Irs2tm1Mfw
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkn1btm1Kin mutation (1 available); any Cdkn1b mutation (25 available)
Irs2tm1Mfw mutation (1 available); any Irs2 mutation (35 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
• beta cell proliferation and the total number of beta cells is increased compared to Irs2 single homozygotes; however the size of individual beta cells is similar to Irs2 single homozygotes
• islet mass, but not islet density, is significantly increased compared to Irs2 single homozygotes

homeostasis/metabolism
• double homozygotes have significantly elevated blood glucose levels at 18 weeks; however this elevation is slight compared to Irs2 single homozygotes
• fasting serum insulin levels are increased




Genotype
MGI:3529778
cx6
Allelic
Composition
Cdkn1btm1Kin/Cdkn1b+
Leprdb/Leprdb
Genetic
Background
involves: C57BL/6J * C57BLKS/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkn1btm1Kin mutation (1 available); any Cdkn1b mutation (25 available)
Leprdb mutation (17 available); any Lepr mutation (121 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological

endocrine/exocrine glands
• islet mass, but not islet density, is significantly increased compared to Lepr single homozygotes
• beta cell proliferation and the total number of beta cells are increased compared to Lepr single homozygotes; however the size of individual beta cells is similar to Lepr single homozygotes

growth/size/body

homeostasis/metabolism
• developed more slowly and to a reduced extent compared to Lepr single homozygotes




Genotype
MGI:3529774
cx7
Allelic
Composition
Cdkn1btm1Kin/Cdkn1btm1Kin
Leprdb/Leprdb
Genetic
Background
involves: C57BL/6J * C57BLKS/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdkn1btm1Kin mutation (1 available); any Cdkn1b mutation (25 available)
Leprdb mutation (17 available); any Lepr mutation (121 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological

endocrine/exocrine glands
• islet mass, but not islet density, is significantly increased compared to Lepr single homozygotes
• beta cell proliferation and the total number of beta cells are increased compared to Lepr single homozygotes; however the size of individual beta cells is similar to Lepr single homozygotes

growth/size/body

homeostasis/metabolism
• hyperlipidemia similar to Lepr single homozygotes is seen; however, double homozygotes do not develop hyperglycemia





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