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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(CAG-Bgeo/GFP)21Lbe
transgene insertion 21, Corrinne Lobe
MGI:3046177
Summary 19 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Atoh7tm1.1(Ascl1)Nlbr/Atoh7+
Tg(Atoh7-cre)360Gla/0
Tg(CAG-Bgeo/GFP)21Lbe/0
either: (involves: 129 * C57BL/6 * FVB/N * SJL) or (involves: 129 * C57BL/6 * CD-1 * FVB/N * SJL) MGI:5529144
cn2
Atoh7tm1.1(Ascl1)Nlbr/Atoh7tm1.1(Ascl1)Nlbr
Tg(Atoh7-cre)360Gla/0
Tg(CAG-Bgeo/GFP)21Lbe/0
either: (involves: 129 * C57BL/6 * FVB/N * SJL) or (involves: 129 * C57BL/6 * CD-1 * FVB/N * SJL) MGI:5529143
cn3
Itga3tm1Hap/Itga3tm1Hap
Tg(CAG-Bgeo/GFP)21Lbe/?
Tg(SFTPC-rtTA)5Jaw/?
Tg(tetO-cre)1Jaw/?
involves: 129 * C57BL/6 MGI:3833134
cn4
Nrp1tm2Ddg/Nrp1tm2Ddg
Or8a1tm28(cre)Mom/Or8a1tm28(cre)Mom
Tg(CAG-Bgeo/GFP)21Lbe/?
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6J MGI:6117236
cn5
Kmt2atm1.1Erns/Kmt2atm1.1Erns
Tg(CAG-Bgeo/GFP)21Lbe/0
involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ MGI:3839881
cn6
Gt(ROSA)26Sortm1(CAG-Kcnj11*,-GFP)Nich/?
Tg(CAG-Bgeo/GFP)21Lbe/0
Tg(Pmch-cre)1Lowl/0
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * FVB/NJ MGI:4887238
cn7
Ucp2tm2.1Lowl/Ucp2tm2.1Lowl
Tg(CAG-Bgeo/GFP)21Lbe/0
Tg(Pmch-cre)1Lowl/0
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6 * FVB/NJ MGI:4887239
cn8
Barhl2tm1Gan/Barhl2tm2(cre)Gan
Tg(CAG-Bgeo/GFP)21Lbe/0
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6J MGI:3841420
cn9
Slc17a6tm1Lowl/Slc17a6tm1Lowl
Tg(CAG-Bgeo/GFP)21Lbe/0
Tg(Nr5a1-cre)2Lowl/0
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * FVB MGI:4442973
cn10
Bhlhe22tm3.1(cre)Meg/Bhlhe22tm1Meg
Tg(CAG-Bgeo/GFP)21Lbe/0
involves: 129S1/Sv * 129X1/SvJ MGI:4440936
cn11
Fat3tm1.2Good/Fat3tm1.2Good
Ptf1atm1.1(cre)Cvw/Ptf1a+
Tg(CAG-Bgeo/GFP)21Lbe/0
involves: 129S1/Sv * 129X1/SvJ MGI:5295428
cn12
Fscn1Gt(OST124903)Lex/Fscn1Gt(OST124903)Lex
Tg(CAG-Bgeo/GFP)21Lbe/0
Tg(Tyr-cre)1Lru/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2 MGI:6209605
cn13
Chd4tm1.1Kge/Chd4tm1.2Kge
Tg(CAG-Bgeo/GFP)21Lbe/0
Tg(Lck-cre)1Cwi/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL MGI:3713384
cn14
Camkk2tm2.1Kpg/Camkk2tm2.1Kpg
Tg(CAG-Bgeo/GFP)21Lbe/0
Tg(Pomc1-cre)1Gsb/0
involves: 129S1/Sv * 129X1/SvJ * FVB/N MGI:4946517
cn15
Bhlhe22tm1Gan/Bhlhe22tm2(cre)Gan
Tg(CAG-Bgeo/GFP)21Lbe/0
involves: 129S/Sv * 129X1/SvJ * C57BL/6J MGI:3830525
cn16
Shox2tm1.1(cre)Oki/Shox2+
Tg(CAG-Bgeo/GFP)21Lbe/0
Vsx2tm1(DTA)Kash/Vsx2+
involves: 129S/SvEv * 129X1/SvJ * C57BL/6J MGI:5576700
cn17
Ntrk2tm2Kln/Ntrk2tm2Kln
Slc1a3tm1(cre/ERT2)Mgoe/?
Tg(CAG-Bgeo/GFP)21Lbe/?
involves: 129/Sv * C57BL/6 * SJL MGI:3830092
cn18
Nkx6-1tm1Jlr/Nkx6-1tm1.1Msan
Tg(CAG-Bgeo/GFP)21Lbe/0
Tg(Neurog3-cre)C1Able/0
involves: 129/Sv * C57BL/6 * SJL MGI:5501186
cx19
Cacnb2tm1.1Mfre/Cacnb2tm1.1Mfre
Tg(CAG-Bgeo/GFP)21Lbe/?
involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6N * FVB/N MGI:3762359


Genotype
MGI:5529144
cn1
Allelic
Composition
Atoh7tm1.1(Ascl1)Nlbr/Atoh7+
Tg(Atoh7-cre)360Gla/0
Tg(CAG-Bgeo/GFP)21Lbe/0
Genetic
Background
either: (involves: 129 * C57BL/6 * FVB/N * SJL) or (involves: 129 * C57BL/6 * CD-1 * FVB/N * SJL)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Atoh7tm1.1(Ascl1)Nlbr mutation (0 available); any Atoh7 mutation (9 available)
Tg(Atoh7-cre)360Gla mutation (0 available)
Tg(CAG-Bgeo/GFP)21Lbe mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• small autonomous loss
• delayed retinal ganglion cell differentiation
• however, adult mice exhibit normal proportion of retinal ganglion cells

nervous system
• small autonomous loss




Genotype
MGI:5529143
cn2
Allelic
Composition
Atoh7tm1.1(Ascl1)Nlbr/Atoh7tm1.1(Ascl1)Nlbr
Tg(Atoh7-cre)360Gla/0
Tg(CAG-Bgeo/GFP)21Lbe/0
Genetic
Background
either: (involves: 129 * C57BL/6 * FVB/N * SJL) or (involves: 129 * C57BL/6 * CD-1 * FVB/N * SJL)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Atoh7tm1.1(Ascl1)Nlbr mutation (0 available); any Atoh7 mutation (9 available)
Tg(Atoh7-cre)360Gla mutation (0 available)
Tg(CAG-Bgeo/GFP)21Lbe mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• increased retinal apoptosis at E12.5 to E16.5
• cell autonomous phenotype
• cell nonautonomous phenotype
• at E12.5 and E13.5, retinal progenitor cells exhibit a block to cell cycle progression and retinal ganglion cell differentiation

nervous system
• cell autonomous phenotype
• cell nonautonomous phenotype

cellular
• at E12.5 and E13.5, retinal progenitor cells exhibit a block to cell cycle progression
• increased retinal apoptosis at E12.5 to E16.5




Genotype
MGI:3833134
cn3
Allelic
Composition
Itga3tm1Hap/Itga3tm1Hap
Tg(CAG-Bgeo/GFP)21Lbe/?
Tg(SFTPC-rtTA)5Jaw/?
Tg(tetO-cre)1Jaw/?
Genetic
Background
involves: 129 * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Itga3tm1Hap mutation (0 available); any Itga3 mutation (52 available)
Tg(CAG-Bgeo/GFP)21Lbe mutation (2 available)
Tg(SFTPC-rtTA)5Jaw mutation (4 available)
Tg(tetO-cre)1Jaw mutation (5 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
respiratory system
• epithelial to mesenchymal transition results from bleomycin-mediated injury of the lung
• only 1.4% of GFP+, epithelium derived cells express mesenchyme markers 17 days after bleomycin injury compared to 7.0% in controls




Genotype
MGI:6117236
cn4
Allelic
Composition
Nrp1tm2Ddg/Nrp1tm2Ddg
Or8a1tm28(cre)Mom/Or8a1tm28(cre)Mom
Tg(CAG-Bgeo/GFP)21Lbe/?
Genetic
Background
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nrp1tm2Ddg mutation (1 available); any Nrp1 mutation (81 available)
Or8a1tm28(cre)Mom mutation (2 available); any Or8a1 mutation (69 available)
Tg(CAG-Bgeo/GFP)21Lbe mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• olfactory sensory neurons expressing the null allele of Nrp1 have an altered and variable pattern of glomeruli formation in the olfactory bulb, including ectopic glomeruli, but the labeled glomeruli do not show an anterior shift relative to Nrp1 wild type controls




Genotype
MGI:3839881
cn5
Allelic
Composition
Kmt2atm1.1Erns/Kmt2atm1.1Erns
Tg(CAG-Bgeo/GFP)21Lbe/0
Genetic
Background
involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kmt2atm1.1Erns mutation (0 available); any Kmt2a mutation (135 available)
Tg(CAG-Bgeo/GFP)21Lbe mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• subventricular neural stem cells treated in culture with adenoviral cre exhibit decreased differentiation compared to wild-type cells
• under differentiation condition, cultured subventricular zone cells treated with adenovirus cre produce 2-fold more oligodendrocytes and 50% more astrocytes than similarly treated wild-type cells
• however, proliferation and apoptosis rates are normal
• under differentiation condition, cultured subventricular zone cells treated with adenovirus cre produce 3-fold fewer Tuj1+ (marking neuron precursor cells) compared similarly treated wild-type cells

cellular
• subventricular neural stem cells treated in culture with adenoviral cre exhibit decreased differentiation compared to wild-type cells
• under differentiation condition, cultured subventricular zone cells treated with adenovirus cre produce 2-fold more oligodendrocytes and 50% more astrocytes than similarly treated wild-type cells
• however, proliferation and apoptosis rates are normal




Genotype
MGI:4887238
cn6
Allelic
Composition
Gt(ROSA)26Sortm1(CAG-Kcnj11*,-GFP)Nich/?
Tg(CAG-Bgeo/GFP)21Lbe/0
Tg(Pmch-cre)1Lowl/0
Genetic
Background
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * FVB/NJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm1(CAG-Kcnj11*,-GFP)Nich mutation (0 available); any Gt(ROSA)26Sor mutation (942 available)
Tg(CAG-Bgeo/GFP)21Lbe mutation (2 available)
Tg(Pmch-cre)1Lowl mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
N
• 8-week-old male mutants do not show differences in body weight, daily food intake, ad libitum-fed blood glucose levels, or overnight fasted blood glucose levels
• 8-week-old males display impaired glucose tolerance (elevated blood glucose after injection of glucose at 2 g/kg body weight) compared to control littermates
• no alterations in pancreatic beta cells is observed due to ectopic cre expression resulting in mutant Kcnj11 expression in beta cells

nervous system
• only about 14% of Pmch neurons show spontaneous action potentials at 5 mM glucose in brain slice preparations compared to 30% of neurons in wild-type preparations, indicating disrupted glucose-sensing
• membrane resistance of Pmch neurons is significantly reduced relative to wild-type neurons at 5 mM glucose
• almost all neurons do not hyperpolarize when extracellular glucose is reduced from 5 to 1 mM whereas around 70% of control neurons hyperpolarize under these conditions, indicating disrupted glucose-sensing
• glucose-induced depolarization is abrogated in Pmch neurons, but is readily observed in control Pmch neurons, indicating disrupted glucose-sensing




Genotype
MGI:4887239
cn7
Allelic
Composition
Ucp2tm2.1Lowl/Ucp2tm2.1Lowl
Tg(CAG-Bgeo/GFP)21Lbe/0
Tg(Pmch-cre)1Lowl/0
Genetic
Background
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6 * FVB/NJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(CAG-Bgeo/GFP)21Lbe mutation (2 available)
Tg(Pmch-cre)1Lowl mutation (2 available)
Ucp2tm2.1Lowl mutation (1 available); any Ucp2 mutation (39 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
N
• 8-week-old male mutants do not show differences in body weight or daily food intake
• ad libitum-fed and overnight fasted blood glucose levels of 8-week-old male mutants are significantly reduced relative to controls
• during glucose tolerance tests, insulin levels are decreased relative to controls, suggesting that decreased glucose levels are not the result of increased insulin secretion
• 8-week-old males display improved glucose tolerance (after injection of glucose at 2 g/kg body weight), with a significantly reduced rise in blood glucose levels relative to controls
• no alterations in pancreatic beta cells is observed due to ectopic cre expression resulting in Ucp2 deletion in beta cells

nervous system
• about 44% of Pmch neurons fire spontaneously at 5 mM glucose, increased from around 30% of control neurons
• membrane potential of Pmch neurons displays enhanced glucose-induced depolarization in response to different glucose concentrations (left-shifted dose-response curve to glucose)




Genotype
MGI:3841420
cn8
Allelic
Composition
Barhl2tm1Gan/Barhl2tm2(cre)Gan
Tg(CAG-Bgeo/GFP)21Lbe/0
Genetic
Background
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Barhl2tm1Gan mutation (0 available); any Barhl2 mutation (15 available)
Barhl2tm2(cre)Gan mutation (0 available); any Barhl2 mutation (15 available)
Tg(CAG-Bgeo/GFP)21Lbe mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• loss of 95% of Barhl2 lineage cells

nervous system
• loss of 95% of Barhl2 lineage cells




Genotype
MGI:4442973
cn9
Allelic
Composition
Slc17a6tm1Lowl/Slc17a6tm1Lowl
Tg(CAG-Bgeo/GFP)21Lbe/0
Tg(Nr5a1-cre)2Lowl/0
Genetic
Background
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * FVB
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Slc17a6tm1Lowl mutation (2 available); any Slc17a6 mutation (59 available)
Tg(CAG-Bgeo/GFP)21Lbe mutation (2 available)
Tg(Nr5a1-cre)2Lowl mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
adipose tissue
• when fed a high fat diet, mice exhibit a slight increase in fat stores

behavior/neurological
• when fed a high fat diet, mice exhibit a slight increase in food intake

growth/size/body
• when fed a high fat diet, mice exhibit a slight increase in fat stores
• mice exhibit a greater increase in weight when fed a high fat diet compared to wild-type mice

homeostasis/metabolism
• after a 24 hour fast, mice exhibit decreased blood glucose levels (males, 55+/-3 compared to 68+/-5 mg/dl in wild-type mice; females 53+/-2 compared to 67+/-5 mg/dl in wild-type mice)
• acute administration of insulin induces hypoglycemia
• mice exhibit impaired fasting-mediated increase in pancreatic hormone glucagon
• following hypoglycemia, mice fail to exhibit an increase in plasma epinephrine levels
• during fasting and following hypoglycemia, mice fail to exhibit an increase in plasma glucagons compared to wild-type mice
• glucose plasma levels fail to increase following central administration of 2-deoxyglucose as in wild-type mice
• however, the hyperhagic response initiated by central administration of 2-deoxyglucose is normal

nervous system
• neurons do not possess any glutamatergic excitatory postsynaptic current




Genotype
MGI:4440936
cn10
Allelic
Composition
Bhlhe22tm3.1(cre)Meg/Bhlhe22tm1Meg
Tg(CAG-Bgeo/GFP)21Lbe/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bhlhe22tm1Meg mutation (0 available); any Bhlhe22 mutation (12 available)
Bhlhe22tm3.1(cre)Meg mutation (0 available); any Bhlhe22 mutation (12 available)
Tg(CAG-Bgeo/GFP)21Lbe mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• in the superficial laminae of spinal cord, there are significantly fewer lacZ-marked neurons compared to controls; significant loss of cell bodies and neuropil is observed




Genotype
MGI:5295428
cn11
Allelic
Composition
Fat3tm1.2Good/Fat3tm1.2Good
Ptf1atm1.1(cre)Cvw/Ptf1a+
Tg(CAG-Bgeo/GFP)21Lbe/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fat3tm1.2Good mutation (0 available); any Fat3 mutation (240 available)
Ptf1atm1.1(cre)Cvw mutation (1 available); any Ptf1a mutation (30 available)
Tg(CAG-Bgeo/GFP)21Lbe mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• amacrine cells retain two processes after reaching the inner plexiform layer unlike unipolar wild-type cells
• amacrine cells fail to retract trailing processes upon reaching the inner plexiform layer
• amacrine cells develop a second arbor that extends to the outer misplaced plexiform layer

vision/eye
• amacrine cells retain two processes after reaching the inner plexiform layer unlike unipolar wild-type cells
• amacrine cells fail to retract trailing processes upon reaching the inner plexiform layer
• amacrine cells develop a second arbor that extends to the outer misplaced plexiform layer
• amacrine cells form two additional plexiform layers (inner and outer misplaced plexiform layers) compared with wild-type mice




Genotype
MGI:6209605
cn12
Allelic
Composition
Fscn1Gt(OST124903)Lex/Fscn1Gt(OST124903)Lex
Tg(CAG-Bgeo/GFP)21Lbe/0
Tg(Tyr-cre)1Lru/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fscn1Gt(OST124903)Lex mutation (1 available); any Fscn1 mutation (42 available)
Tg(CAG-Bgeo/GFP)21Lbe mutation (2 available)
Tg(Tyr-cre)1Lru mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• melanoblasts in E14.5 skin explants show significantly reduced cell migration speed and euclidean distance travelled relative to wild-type controls
• ~30% of melanoblasts migrate with a speed slower than 0.5 um/minute versus fewer than 10% of melanoblasts in wild-type explants
• however, directionality (the ratio between the euclidean distance and total distance travelled) is normal
• melanoblasts in E14.5 live skin explants are slightly smaller than wild type
• the rate of pseudopod generation in melanoblasts is modestly reduced but the lifetime of pseudopods is increased
• melanoblasts extend thinner protrusions with a smaller cross-sectional width than wild type controls
• thinner pseudopodia are less dynamic (longer-lived) leading to slower melanoblast migration

cellular
• melanoblasts in E14.5 skin explants show significantly reduced cell migration speed and euclidean distance travelled relative to wild-type controls
• ~30% of melanoblasts migrate with a speed slower than 0.5 um/minute versus fewer than 10% of melanoblasts in wild-type explants
• however, directionality (the ratio between the euclidean distance and total distance travelled) is normal

nervous system
• melanoblasts in E14.5 live skin explants are slightly smaller than wild type
• the rate of pseudopod generation in melanoblasts is modestly reduced but the lifetime of pseudopods is increased
• melanoblasts extend thinner protrusions with a smaller cross-sectional width than wild type controls
• thinner pseudopodia are less dynamic (longer-lived) leading to slower melanoblast migration




Genotype
MGI:3713384
cn13
Allelic
Composition
Chd4tm1.1Kge/Chd4tm1.2Kge
Tg(CAG-Bgeo/GFP)21Lbe/0
Tg(Lck-cre)1Cwi/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Chd4tm1.1Kge mutation (0 available); any Chd4 mutation (58 available)
Chd4tm1.2Kge mutation (0 available); any Chd4 mutation (58 available)
Tg(CAG-Bgeo/GFP)21Lbe mutation (2 available)
Tg(Lck-cre)1Cwi mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• progressive decrease in cycling T cells is observed from second to third cell division in vitro, along with large number of nonblast T cells that appear to fail to enter cell cycle
• a 5- to 7-fold decrease in proliferation is observed relative to wild-type cells in vitro after 48 hours of TCR/CD3 stimulation; fewer mutant cells are in S phase

immune system
• a 5- to 7-fold decrease in proliferation is observed relative to wild-type cells in vitro after 48 hours of TCR/CD3 stimulation; fewer mutant cells are in S phase

hematopoietic system
• a 5- to 7-fold decrease in proliferation is observed relative to wild-type cells in vitro after 48 hours of TCR/CD3 stimulation; fewer mutant cells are in S phase




Genotype
MGI:4946517
cn14
Allelic
Composition
Camkk2tm2.1Kpg/Camkk2tm2.1Kpg
Tg(CAG-Bgeo/GFP)21Lbe/0
Tg(Pomc1-cre)1Gsb/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Camkk2tm2.1Kpg mutation (0 available); any Camkk2 mutation (40 available)
Tg(CAG-Bgeo/GFP)21Lbe mutation (2 available)
Tg(Pomc1-cre)1Gsb mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
N
• energy homeostasis and glucose handling are normal




Genotype
MGI:3830525
cn15
Allelic
Composition
Bhlhe22tm1Gan/Bhlhe22tm2(cre)Gan
Tg(CAG-Bgeo/GFP)21Lbe/0
Genetic
Background
involves: 129S/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bhlhe22tm1Gan mutation (0 available); any Bhlhe22 mutation (12 available)
Bhlhe22tm2(cre)Gan mutation (0 available); any Bhlhe22 mutation (12 available)
Tg(CAG-Bgeo/GFP)21Lbe mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• at P0, no Bhlhe22-expression fibers are detected in the medullary pyramidal tract unlike in wild-type mice
• in adults, few Bhlhe22-expression fibers are detected in the medullary pyramidal tract unlike in wild-type mice
• Bhlhe22-expression fibers present in the decussation do not enter the ventral dorsal funiculus of the spinal cord unlike in wild-type mice
• fewer than normal subcerebral projection neurons enter the medullary pyramidal tract while caudal corticospinal motor neurons fail to enter the tract




Genotype
MGI:5576700
cn16
Allelic
Composition
Shox2tm1.1(cre)Oki/Shox2+
Tg(CAG-Bgeo/GFP)21Lbe/0
Vsx2tm1(DTA)Kash/Vsx2+
Genetic
Background
involves: 129S/SvEv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shox2tm1.1(cre)Oki mutation (0 available); any Shox2 mutation (19 available)
Tg(CAG-Bgeo/GFP)21Lbe mutation (2 available)
Vsx2tm1(DTA)Kash mutation (0 available); any Vsx2 mutation (23 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• number of Shox2-expressing V2a interneurons is reduced by 98%; total number of Shox2-expressing interneurons is reduced by >80%
• variability in locomotor parameters (cycle period, burst duration, amplitude) that are observed in isolated neonatal spinal cords exposed to low NMDA concentrations is increased in mutants compared to controls; higher NMDA concentrations reduce this variability
• other parameters such as burst frequency and flexor-extensor alternation are not significantly different




Genotype
MGI:3830092
cn17
Allelic
Composition
Ntrk2tm2Kln/Ntrk2tm2Kln
Slc1a3tm1(cre/ERT2)Mgoe/?
Tg(CAG-Bgeo/GFP)21Lbe/?
Genetic
Background
involves: 129/Sv * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ntrk2tm2Kln mutation (0 available); any Ntrk2 mutation (66 available)
Slc1a3tm1(cre/ERT2)Mgoe mutation (0 available); any Slc1a3 mutation (66 available)
Tg(CAG-Bgeo/GFP)21Lbe mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• synaptic contacts appear to be normal for neurons arising in hippocampus from radial glial cells after treatment with tamoxifen




Genotype
MGI:5501186
cn18
Allelic
Composition
Nkx6-1tm1Jlr/Nkx6-1tm1.1Msan
Tg(CAG-Bgeo/GFP)21Lbe/0
Tg(Neurog3-cre)C1Able/0
Genetic
Background
involves: 129/Sv * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nkx6-1tm1.1Msan mutation (1 available); any Nkx6-1 mutation (4 available)
Nkx6-1tm1Jlr mutation (0 available); any Nkx6-1 mutation (4 available)
Tg(CAG-Bgeo/GFP)21Lbe mutation (2 available)
Tg(Neurog3-cre)C1Able mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die within the first few days after birth

endocrine/exocrine glands
N
• mice do not exhibit endocrine-to-acinar fate conversion
• beta cells exhibit normal cell proliferation and apoptosis
• beta cell differentiation is impaired with insulin+ cells that are polyhormonal and ectopically express alpha cell markers unlike in control cells
• due to reduced differentiation without an effect on proliferation and apoptosis

homeostasis/metabolism

cellular
• beta cell differentiation is impaired with insulin+ cells that are polyhormonal and ectopically express alpha cell markers unlike in control cells




Genotype
MGI:3762359
cx19
Allelic
Composition
Cacnb2tm1.1Mfre/Cacnb2tm1.1Mfre
Tg(CAG-Bgeo/GFP)21Lbe/?
Genetic
Background
involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6N * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cacnb2tm1.1Mfre mutation (0 available); any Cacnb2 mutation (50 available)
Tg(CAG-Bgeo/GFP)21Lbe mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die following E10.5 and are completely absorbed by E11.5
• however, treatment with a calcium channel agonist, 1 umol/L (-)-BayK 8644, partially rescues embryonic lethality with mice surviving until the end of E11.5

cardiovascular system
• at E10.5, a stenosis is frequently observed between the emerging right ventricle and the outflow tract
• at E10.5, mice display abnormal heart looping
• at E10.5, mice display abnormal heart looping with amorphous heart tubes lying distorted within the pericardial cavity, and a stenosis is frequently observed between the emerging right ventricle and the outflow tract
• at E10.5, pericardial effusion is associated with hemorrhages
• at E10.5, hearts only exhibit barely noticeable tremors without any noticeable ejection volume
• at E10.5, pericardial effusion is associated with hemorrhages
• 63+/-2.88 beats per minute compared to 120+/-3.15 beats per minute in wild-type mice
• however, no difference in heart rate is observed at E9.5
• at E10.5, L-type calcium channel activity and calcium-induced calcium release is impaired resulting in diminished heart pumping
• calcium channel current density is reduced compared to in wild-type mice
• unlike wild-type cardiomyocytes, E9.5 cardiomyocytes fail to respond to catecholamine treatment

embryo
• unlike in wild-type mice, embryos size does not double between E9.5 and E10.5
• at E9.5, vascular remodeling of the primary capillary plexus fails to occur and a honeycomb-like network of tubules with enlarged and uniform diameters forms in the extra- and intraembryonic vasculature

nervous system
• between E9.5 and E10.5

growth/size/body
• between E9.5 and E10.5, mice exhibit poor growth of facial primordial tissue
• unlike in wild-type mice, embryos size does not double between E9.5 and E10.5

craniofacial
• between E9.5 and E10.5, mice exhibit poor growth of facial primordial tissue

homeostasis/metabolism
• at E10.5, pericardial effusion is associated with hemorrhages

hematopoietic system
• very few hemangioblasts are found in the blood vessels of the yolk sac

muscle





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory