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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(CDX2-cre)101Erf
transgene insertion 101, Eric R Fearon
MGI:3696953
Summary 8 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Mstntm3.1Sjl/Mstntm3.1Sjl
Tg(CDX2-cre)101Erf/0
B6.Cg-Mstntm3.1Sjl Tg(CDX2-cre)101Erf/Sjl MGI:5902401
cn2
Apctm1Tno/Apc+
Il23atm1Ngh/Il23atm1Ngh
Tg(CDX2-cre)101Erf/0
involves: 129 * 129S4/SvJae * C57BL/6J * SJL/J MGI:5446624
cn3
Apctm1Tno/Apc+
Il17ratm1Koll/Il17ratm1Koll
Tg(CDX2-cre)101Erf/0
involves: 129 * 129S4/SvJae * C57BL/6J * SJL/J MGI:5446625
cn4
Neurog3tm3.1Ggr/Neurog3tm3.1Ggr
Tg(CDX2-cre)101Erf/0
involves: 129S2/SvPas * C57BL/6J * SJL/J MGI:6711505
cn5
Apctm1Tno/Apc+
Il23rtm1.2Trin/Il23rtm1.2Trin
Tg(CDX2-cre)101Erf/0
involves: 129S4/SvJae * C57BL/6 * C57BL/6J * SJL/J MGI:5446693
cn6
Apctm1Tno/Apc+
Tg(CDX2-cre)101Erf/0
involves: 129S4/SvJae * C57BL/6 * SJL MGI:3844311
cn7
Apctm1Tno/Apctm1Tno
Tg(CDX2-cre)101Erf/0
involves: 129S4/SvJae * C57BL/6 * SJL MGI:3844313
cn8
Psmf1tm1c(EUCOMM)Hmgu/Psmf1tm1c(EUCOMM)Hmgu
Tg(CDX2-cre)101Erf/0
involves: C57BL/6J * C57BL/6N * SJL/J MGI:6838400


Genotype
MGI:5902401
cn1
Allelic
Composition
Mstntm3.1Sjl/Mstntm3.1Sjl
Tg(CDX2-cre)101Erf/0
Genetic
Background
B6.Cg-Mstntm3.1Sjl Tg(CDX2-cre)101Erf/Sjl
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mstntm3.1Sjl mutation (0 available); any Mstn mutation (33 available)
Tg(CDX2-cre)101Erf mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• in the presence of this cre deleter, which expresses in tissues posterior to the umbilicus but not anterior to it, floxed homozygotes have reduced serum levels of myostatin, with females having 26 +/- 2 ng/ml and males 42.7 +/- 2.6 nm/ml, compared with wild-type values of 62.2 and 82.9 ng/ml respectively, and this results from ablated expression from posterior muscles but relatively normal expression from anterior muscles. The levels found in females, but not males, is lower than the levels found in haploinsufficient females heterozygous for a null allele.

muscle
• two posteriorly located muscles, quadriceps and gastrocnemius, have dramatically higher weights than those of control mice at 10 weeks of age, while the anteriorly located muscles, pectoralis and triceps, have a slight increase, likely due to the decreased levels of serum myostatin. The increase in quadriceps size in both males and females is statistically larger in mice homozygous for a null allele than in these compartmentally null mice indicating that serum myostatin generated from anterior muscles has an impact, albeit a minority impact, on posterior muscles
• the gastrocnemius, assessed from females, has an increase in the total number of muscle fibers from an average of 8,802 in the absence of cre to 13,079 in the presence of cre
• the gastrocnemius, assessed from females, has an increase in the fiber diameter of muscle fibers averaging 16.5% larger than the muscle fibers in the absence of cre




Genotype
MGI:5446624
cn2
Allelic
Composition
Apctm1Tno/Apc+
Il23atm1Ngh/Il23atm1Ngh
Tg(CDX2-cre)101Erf/0
Genetic
Background
involves: 129 * 129S4/SvJae * C57BL/6J * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apctm1Tno mutation (6 available); any Apc mutation (154 available)
Il23atm1Ngh mutation (0 available); any Il23a mutation (25 available)
Tg(CDX2-cre)101Erf mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• reduced colorectal tumor multiplicity and grown due to reduced cell proliferation compared with Apctm1Tno/Apc+ Tg(CDX2-cre)101Erf mice




Genotype
MGI:5446625
cn3
Allelic
Composition
Apctm1Tno/Apc+
Il17ratm1Koll/Il17ratm1Koll
Tg(CDX2-cre)101Erf/0
Genetic
Background
involves: 129 * 129S4/SvJae * C57BL/6J * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apctm1Tno mutation (6 available); any Apc mutation (154 available)
Il17ratm1Koll mutation (0 available); any Il17ra mutation (46 available)
Tg(CDX2-cre)101Erf mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• reduced colorectal tumor multiplicity and grown compared to in Apctm1Tno/Apc+ Tg(CDX2-cre)101Erf mice




Genotype
MGI:6711505
cn4
Allelic
Composition
Neurog3tm3.1Ggr/Neurog3tm3.1Ggr
Tg(CDX2-cre)101Erf/0
Genetic
Background
involves: 129S2/SvPas * C57BL/6J * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Neurog3tm3.1Ggr mutation (0 available); any Neurog3 mutation (18 available)
Tg(CDX2-cre)101Erf mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
digestive/alimentary system
N
• normal sensitivity to DSS-induced colitis




Genotype
MGI:5446693
cn5
Allelic
Composition
Apctm1Tno/Apc+
Il23rtm1.2Trin/Il23rtm1.2Trin
Tg(CDX2-cre)101Erf/0
Genetic
Background
involves: 129S4/SvJae * C57BL/6 * C57BL/6J * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apctm1Tno mutation (6 available); any Apc mutation (154 available)
Il23rtm1.2Trin mutation (0 available); any Il23r mutation (68 available)
Tg(CDX2-cre)101Erf mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
neoplasm
• reduced colorectal tumor multiplicity and grown compared to in Apctm1Tno/Apc+ Tg(CDX2-cre)101Erf mice




Genotype
MGI:3844311
cn6
Allelic
Composition
Apctm1Tno/Apc+
Tg(CDX2-cre)101Erf/0
Genetic
Background
involves: 129S4/SvJae * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apctm1Tno mutation (6 available); any Apc mutation (154 available)
Tg(CDX2-cre)101Erf mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• 36% (13/36) animals survived to 300 days of observation; 3 died and 20 were euthanized upon signs of distress

growth/size/body
• males show inhibited weight gain after 120 days

neoplasm
• mice show around 10 tumors
• an average of 5-8 tumors are found in colon and rectum, wit some tumors being observed in the cecum and distal small intestine
• colorectal tumors may be observed at early time points
• male mice have about 60% more colon tumors than controls
• a small number of mice also develop mammary tumors

digestive/alimentary system
• greater than half the animals observed developed rectal prolapse with intermittent bleeding
• an average of 5-8 tumors are found in colon and rectum, wit some tumors being observed in the cecum and distal small intestine
• colorectal tumors may be observed at early time points
• male mice have about 60% more colon tumors than controls
• some (3) animals died during the observation period from intestinal obstruction by tumor

hematopoietic system
• mice exhibit mild anemia
• mice displaying mild anemia show hematocrits in range of 33 to 35% compared to around 45% in controls

endocrine/exocrine glands
• a small number of mice also develop mammary tumors

integument
• a small number of mice also develop mammary tumors

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
colorectal cancer DOID:9256 OMIM:114500
J:126018




Genotype
MGI:3844313
cn7
Allelic
Composition
Apctm1Tno/Apctm1Tno
Tg(CDX2-cre)101Erf/0
Genetic
Background
involves: 129S4/SvJae * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Apctm1Tno mutation (6 available); any Apc mutation (154 available)
Tg(CDX2-cre)101Erf mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• embryonic lethality is observed




Genotype
MGI:6838400
cn8
Allelic
Composition
Psmf1tm1c(EUCOMM)Hmgu/Psmf1tm1c(EUCOMM)Hmgu
Tg(CDX2-cre)101Erf/0
Genetic
Background
involves: C57BL/6J * C57BL/6N * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Psmf1tm1c(EUCOMM)Hmgu mutation (0 available); any Psmf1 mutation (11 available)
Tg(CDX2-cre)101Erf mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• all mice die by 3 to 4 weeks of age

behavior/neurological
• mice begin to develop progressive neuromotor phenotypes around P6, characterized by spasticity, rigid muscle tone, strong tremor, and severely impaired righting response
• severely impaired righting response
• mice exhibit hindlimb clasping between episodes of tremor when picked up by tails
• strong tremor
• mice are only able to move using their front legs since their hind limbs are hyperextended and paralyzed

muscle
• rigid muscle tone





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