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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Mpz-cre)26Mes
transgene insertion 26, Albee Messing
MGI:2450448
Summary 23 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Dag1tm2Kcam/Dag1tm2Kcam
Itgb4tm1Mfel/Itgb4tm1Mfel
Tg(Mpz-cre)26Mes/0
involves: 129 * C57BL/6 * FVB/N MGI:3804181
cn2
Dag1tm2Kcam/Dag1tm2Kcam
Tg(Mpz-cre)26Mes/0
involves: 129 * C57BL/6 * FVB/N MGI:3804182
cn3
Itga3tm1Hap/Itga3tm1Hap
Itga6tm2Egl/Itga6tm2Egl
Tg(Mpz-cre)26Mes/0
involves: 129 * C57BL/6 * FVB/NTac MGI:5563094
cn4
Itga3tm1Hap/Itga3tm1Hap
Tg(Mpz-cre)26Mes/0
involves: 129 * C57BL/6 * FVB/NTac MGI:5563095
cn5
Sirt2tm1.1Auw/Sirt2tm1.1Auw
Tg(Mpz-cre)26Mes/0
involves: 129 * C57BL/6J * FVB/N MGI:5295752
cn6
Lamc1tm1Strl/Lamc1tm1Strl
Tg(Mpz-cre)26Mes/0
involves: 129P2/OlaHsd * C57BL/6 * FVB/N MGI:2683489
cn7
Dlg1tm1Rlh/Dlg1tm1Rlh
Tg(Mpz-cre)26Mes/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/NTac MGI:5558043
cn8
Dlg1tm1Rlh/Dlg1tm1.1Rlh
Tg(Mpz-cre)26Mes/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/NTac MGI:5558044
cn9
Itga6tm2Egl/Itga6tm2Egl
Itga7tm1Umr/Itga7tm1Umr
Tg(Mpz-cre)26Mes/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/NTac MGI:5563096
cn10
Itgb4tm1Mfel/Itgb4tm1.1Mfel
Tg(Mpz-cre)26Mes/0
involves: 129S2/SvPas * C57BL/6 * FVB/N MGI:3804180
cn11
Itgb4tm1Mfel/Itgb4tm1Mfel
Tg(Mpz-cre)26Mes/0
involves: 129S2/SvPas * C57BL/6 * FVB/N MGI:3804179
cn12
Mtmr2tm1Abol/Mtmr2tm1Abol
Tg(Mpz-cre)26Mes/0
involves: 129S2/SvPas * FVB/N MGI:3513669
cn13
Col1a1tm1(CAG-Sirt2)Jmi/Col1a1+
Tg(Mpz-cre)26Mes/0
involves: 129S4/SvJae * C57BL/6 * FVB/N MGI:5295750
cn14
Resttm1.1Yasu/Rest+
Tg(Mpz-cre)26Mes/0
involves: 129S4/SvJae * C57BL/6 * FVB/NTac MGI:6241492
cn15
Resttm1.1Yasu/Resttm1.1Yasu
Tg(Mpz-cre)26Mes/0
involves: 129S4/SvJae * C57BL/6 * FVB/NTac MGI:6241493
cn16
Pi4kbtm1.1Tbal/Pi4kbtm1.1Tbal
Tg(Mpz-cre)26Mes/0
involves: 129S6/SvEvTac * C57BL/6 * FVB MGI:6696059
cn17
Lpin1tm1Rchr/Lpin1tm1Rchr
Tg(Mpz-cre)26Mes/0
involves: 129S6/SvEvTac * FVB/N MGI:3800405
cn18
Rab35tm1.1Vha/Rab35tm1.1Vha
Tg(Mpz-cre)26Mes/0
involves: 129/Sv * 129S4/SvJaeSor * C57BL/6J * FVB/NTac MGI:6467549
cn19
Itga6tm2Egl/Itga6tm2Egl
Tg(Mpz-cre)26Mes/0
involves: C57BL/6 * FVB/NTac MGI:5563093
cn20
Dnm2tm1Ueli/Dnm2tm2.1Ics
Tg(Mpz-cre)26Mes/0
involves: C57BL/6J * C57BL/6N * FVB/NTac MGI:6506449
cn21
Cyth2tm1c(EUCOMM)Wtsi/Cyth2tm1c(EUCOMM)Wtsi
Tg(Mpz-cre)26Mes/0
involves: C57BL/6N * FVB/NTac MGI:6151124
cn22
Nfasctm1Bhat/Nfasctm1Bhat
Tg(Mpz-cre)26Mes/?
involves: FVB/N MGI:3836431
cn23
Gdap1tm1Ics/Gdap1tm1Ics
Tg(Mpz-cre)26Mes/0
involves: FVB/NTac MGI:5789297


Genotype
MGI:3804181
cn1
Allelic
Composition
Dag1tm2Kcam/Dag1tm2Kcam
Itgb4tm1Mfel/Itgb4tm1Mfel
Tg(Mpz-cre)26Mes/0
Genetic
Background
involves: 129 * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dag1tm2Kcam mutation (2 available); any Dag1 mutation (109 available)
Itgb4tm1Mfel mutation (0 available); any Itgb4 mutation (107 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• the inner mesaxon appears disorganized
• abnormally folded myelin with loops, infolding and outfolding is seen in sciatic nerves
• abnormal folding increases with age
• hypomyelination of the ventral roots that is more severe than in single conditional null Dag1tm2Kcam mice
• decrease in myelination becomes evident with age and at 12 months of age includes signs of acute demyelination, myelin degeneration, macrophage infiltration, and remyelination
• macrophages are more numerous in double mutants compared to single conditional null Dag1tm2Kcam mice
• slight but non significant reduction compared to single conditional null Dag1tm2Kcam mice
• slight but non significant increase compared to single conditional null Dag1tm2Kcam mice
• slight but non significant reduction compared to single conditional null Dag1tm2Kcam mice




Genotype
MGI:3804182
cn2
Allelic
Composition
Dag1tm2Kcam/Dag1tm2Kcam
Tg(Mpz-cre)26Mes/0
Genetic
Background
involves: 129 * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dag1tm2Kcam mutation (2 available); any Dag1 mutation (109 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• abnormally folded myelin with loops, infolding and outfolding is seen in sciatic nerves
• hypomyelination of the ventral roots
• decrease in myelination becomes evident with age and at 12 months of age includes signs of acute demyelination, myelin degeneration, macrophage infiltration, and remyelination
• reduced motor action potential amplitude




Genotype
MGI:5563094
cn3
Allelic
Composition
Itga3tm1Hap/Itga3tm1Hap
Itga6tm2Egl/Itga6tm2Egl
Tg(Mpz-cre)26Mes/0
Genetic
Background
involves: 129 * C57BL/6 * FVB/NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Itga3tm1Hap mutation (0 available); any Itga3 mutation (53 available)
Itga6tm2Egl mutation (0 available); any Itga6 mutation (211 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• normal morphology of sciatic nerves and spinal roots with no gross defects in axon sorting and myelination




Genotype
MGI:5563095
cn4
Allelic
Composition
Itga3tm1Hap/Itga3tm1Hap
Tg(Mpz-cre)26Mes/0
Genetic
Background
involves: 129 * C57BL/6 * FVB/NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Itga3tm1Hap mutation (0 available); any Itga3 mutation (53 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• normal morphology of sciatic nerves and spinal roots with no gross defects in axon sorting and myelination




Genotype
MGI:5295752
cn5
Allelic
Composition
Sirt2tm1.1Auw/Sirt2tm1.1Auw
Tg(Mpz-cre)26Mes/0
Genetic
Background
involves: 129 * C57BL/6J * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sirt2tm1.1Auw mutation (1 available); any Sirt2 mutation (27 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Sirt2tm1.1Auw/Sirt2tm1.1Auw Tg(Mpz-cre)26Mes/0 mice display hypomyelination

nervous system
• mice exhibit a transient delay in myelination compared with wild-type mice
• the sciatic nerve is hypomyelinated at P1, P3, and P5
• at P21 and P28, mice exhibit extensive outfoldings in compact myelin located in close vicinity to the paranode
• following nerve crush injury, mice exhibit reduced myelination compared with wild-type mice
• however, mice exhibit normal myelination at P7 and remyelination following nerve crush injury after 28 days

homeostasis/metabolism
• remyelination following nerve crush injury is delayed compared to in wild-type mice
• however, axon regeneration is normal

behavior/neurological
N
• mice exhibit normal function on a rotarod, grip strength, and thermal nociception




Genotype
MGI:2683489
cn6
Allelic
Composition
Lamc1tm1Strl/Lamc1tm1Strl
Tg(Mpz-cre)26Mes/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lamc1tm1Strl mutation (1 available); any Lamc1 mutation (143 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• in mutant nerves, Schwann cells populate the nerve but fail to sort and myelinate axons
• mutant sciatic nerves are undermyelinated even though many Schwann cells are present
• in mutant nerves, Schwann cells populate the nerve but fail to sort and myelinate axons

behavior/neurological




Genotype
MGI:5558043
cn7
Allelic
Composition
Dlg1tm1Rlh/Dlg1tm1Rlh
Tg(Mpz-cre)26Mes/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dlg1tm1Rlh mutation (1 available); any Dlg1 mutation (76 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• at P10, P20 and P45
• however, myelination is normal at P90 and 6 months




Genotype
MGI:5558044
cn8
Allelic
Composition
Dlg1tm1Rlh/Dlg1tm1.1Rlh
Tg(Mpz-cre)26Mes/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dlg1tm1.1Rlh mutation (0 available); any Dlg1 mutation (76 available)
Dlg1tm1Rlh mutation (1 available); any Dlg1 mutation (76 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• mice exhibit normal myelination at P90




Genotype
MGI:5563096
cn9
Allelic
Composition
Itga6tm2Egl/Itga6tm2Egl
Itga7tm1Umr/Itga7tm1Umr
Tg(Mpz-cre)26Mes/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Itga6tm2Egl mutation (0 available); any Itga6 mutation (211 available)
Itga7tm1Umr mutation (0 available); any Itga7 mutation (35 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• delay in radial sorting of axons in the sciatic nerve at P5
• arrest in radial sorting, with axon bundles containing naked, mixed caliber axons
• arrest in radial sorting, with axon bundles containing mixed caliber axons lacking ensheathing Schwann cells and having redundant and detached basal lamina
• cells spread less when plated on laminin compared to wild-type cells
• bundles of naked axons are seen at P15 and P28 in the sciatic nerve




Genotype
MGI:3804180
cn10
Allelic
Composition
Itgb4tm1Mfel/Itgb4tm1.1Mfel
Tg(Mpz-cre)26Mes/0
Genetic
Background
involves: 129S2/SvPas * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Itgb4tm1.1Mfel mutation (0 available); any Itgb4 mutation (107 available)
Itgb4tm1Mfel mutation (0 available); any Itgb4 mutation (107 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• progressive increase in the number of myelin infoldings in the sciatic nerve, digital nerve, and anterior roots after 12 months of age

behavior/neurological
N
• despite loss of expression in Schwann cells, no tremors, gait abnormalities, or motor skill impairments are detected




Genotype
MGI:3804179
cn11
Allelic
Composition
Itgb4tm1Mfel/Itgb4tm1Mfel
Tg(Mpz-cre)26Mes/0
Genetic
Background
involves: 129S2/SvPas * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Itgb4tm1Mfel mutation (0 available); any Itgb4 mutation (107 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• progressive increase in the number of myelin infoldings in the sciatic nerve, digital nerve, and anterior roots after 12 months of age

behavior/neurological
N
• despite loss of expression in Schwann cells, no tremors, gait abnormalities, or motor skill impairments are detected




Genotype
MGI:3513669
cn12
Allelic
Composition
Mtmr2tm1Abol/Mtmr2tm1Abol
Tg(Mpz-cre)26Mes/0
Genetic
Background
involves: 129S2/SvPas * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mtmr2tm1Abol mutation (0 available); any Mtmr2 mutation (38 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• sciatic nerves had myelin outfoldings and recurrent loops in similar numbers and location as Mtmr2tm1.1Abol null mice
• sciatic nerves had myelin outfoldings and recurrent loops in similar numbers and location as Mtmr2tm1.1Abol null mice




Genotype
MGI:5295750
cn13
Allelic
Composition
Col1a1tm1(CAG-Sirt2)Jmi/Col1a1+
Tg(Mpz-cre)26Mes/0
Genetic
Background
involves: 129S4/SvJae * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Col1a1tm1(CAG-Sirt2)Jmi mutation (1 available); any Col1a1 mutation (163 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Delayed remyelination after nerve crush injury in Col1a1tm1(CAG-Sirt2)Jmi/Col1a1tm1(CAG-Sirt2)Jmi Tg(Mpz-cre)26Mes/0 mice

homeostasis/metabolism
• remyelination following nerve crush injury is delayed compared to in wild-type mice
• however, axon regeneration is normal

nervous system
• remyelination following nerve crush injury is delayed compared to in wild-type mice




Genotype
MGI:6241492
cn14
Allelic
Composition
Resttm1.1Yasu/Rest+
Tg(Mpz-cre)26Mes/0
Genetic
Background
involves: 129S4/SvJae * C57BL/6 * FVB/NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Resttm1.1Yasu mutation (1 available); any Rest mutation (96 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation
N
• mice never form white spots including on the belly region




Genotype
MGI:6241493
cn15
Allelic
Composition
Resttm1.1Yasu/Resttm1.1Yasu
Tg(Mpz-cre)26Mes/0
Genetic
Background
involves: 129S4/SvJae * C57BL/6 * FVB/NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Resttm1.1Yasu mutation (1 available); any Rest mutation (96 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation
N
• mice never form white spots including on the belly region




Genotype
MGI:6696059
cn16
Allelic
Composition
Pi4kbtm1.1Tbal/Pi4kbtm1.1Tbal
Tg(Mpz-cre)26Mes/0
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * FVB
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pi4kbtm1.1Tbal mutation (0 available); any Pi4kb mutation (40 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• reduction to almost complete lack of caveolae, missing or severely underdeveloped Schwann cell microvilli, and disorganized Golgi
• in small diameter axons
• disorganization of the Node of Ranvier
• missing or severely underdeveloped Schwann cell microvilli allowing for axon herniation
• disintegration of basal lamina around the Remak bundles
• more nuclei and deduced total lipid content with reduced sphingomyelin and phosphatidylethanolamine

behavior/neurological
• small impairment
• noticeable at 3 weeks after birth
• in hindlimb




Genotype
MGI:3800405
cn17
Allelic
Composition
Lpin1tm1Rchr/Lpin1tm1Rchr
Tg(Mpz-cre)26Mes/0
Genetic
Background
involves: 129S6/SvEvTac * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lpin1tm1Rchr mutation (0 available); any Lpin1 mutation (57 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• accumulation of myelin debris in Schwann cells, increase in the number of mast cells and defects in unmyelinated Schwann cells
• accumulation of lipid-containing particles in the perineurial and endoneurial compartments
• however, unlike Lpin1fld homozygotes no reduction is seen in the number of adipocytes in the epineurium
• strong demyelination of the sciatic nerve similar to Lpin1fld homozygotes
• accumulation of myelin debris in Schwann cells, increase in the number of mast cells and defects in unmyelinated Schwann cells
• reduced motor nerve conduction velocity is accompanied by temporal dispersion and reduction of compound muscle action potentials
• strong reduction in motor nerve conduction velocity of the sciatic nerve at P56

behavior/neurological
• clench toes of the hind feet when lifted by the tail
• develops by 2 weeks of age




Genotype
MGI:6467549
cn18
Allelic
Composition
Rab35tm1.1Vha/Rab35tm1.1Vha
Tg(Mpz-cre)26Mes/0
Genetic
Background
involves: 129/Sv * 129S4/SvJaeSor * C57BL/6J * FVB/NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rab35tm1.1Vha mutation (0 available); any Rab35 mutation (21 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• born at normal Mendelian ratio

nervous system
• normal thickness in sciatic nerves and normal number of myelinated axons at age P20, P30 and P90
• reduced thickness in larger sciatic nerves (>5 micrometer diameter) at age P90
• in sciatic nerves at age P90




Genotype
MGI:5563093
cn19
Allelic
Composition
Itga6tm2Egl/Itga6tm2Egl
Tg(Mpz-cre)26Mes/0
Genetic
Background
involves: C57BL/6 * FVB/NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Itga6tm2Egl mutation (0 available); any Itga6 mutation (211 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• viable

nervous system
• 5% of axons in the sciatic nerve have overly thin myelin for the caliber of the axon
• 25% of axons in the sciatic nerve have overly thick myelin for the caliber of the axon
• in the sciatic nerve, remak bundles contain axons that are greater than 1 um in diameter suggesting a defect in recognition or sorting of axons
• other large caliber axons in the sciatic nerve are sorted properly but not myelinated suggesting a delay in myelination
• some small caliber axons (less than 1 um in diameter) in the sciatic nerve are abnormally myelinated
• 5% of axons in the sciatic nerve have overly thin myelin for the caliber of the axon
• occasional
• cells spread less when plated on laminin compared to wild-type cells
• in the sciatic nerve, remak bundles contain axons that are greater than 1 um in diameter suggesting a defect in recognition or sorting of axons
• other large caliber axons in the sciatic nerve are sorted properly but not myelinated suggesting a delay in myelination
• some small caliber axons (less than 1 um in diameter) in the sciatic nerve are abnormally myelinated
• 5% of axons in the sciatic nerve have overly thin myelin for the caliber of the axon
• 25% of axons in the sciatic nerve have overly thick myelin for the caliber of the axon




Genotype
MGI:6506449
cn20
Allelic
Composition
Dnm2tm1Ueli/Dnm2tm2.1Ics
Tg(Mpz-cre)26Mes/0
Genetic
Background
involves: C57BL/6J * C57BL/6N * FVB/NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dnm2tm1Ueli mutation (0 available); any Dnm2 mutation (100 available)
Dnm2tm2.1Ics mutation (0 available); any Dnm2 mutation (100 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• mice show severe demyelinating neuropathy
• nerves show a strong reduction of myelinated axons at P24, with an increase in the number of sorted myelin-competent axons that are not enwrapped by myelin
• cells with engulfed myelin inclusions, indicative of ongoing demyelination, are commonly seen in nerves at P24
• however, the number of sorted axons and numbers of structural myelin aberrations are not changed
• no morphological changes are seen in tibial nerves or sciatic nerves at P5, indicating normal radial axonal sorting and correct onset of myelination
• electrophysiology shows decreased compound muscle action potential amplitude at P24
• electrophysiology shows reduced motor nerve conduction velocity at P24
• compound sensory nerve conduction velocity and compound sensory amplitude are not detectible in P24 mice




Genotype
MGI:6151124
cn21
Allelic
Composition
Cyth2tm1c(EUCOMM)Wtsi/Cyth2tm1c(EUCOMM)Wtsi
Tg(Mpz-cre)26Mes/0
Genetic
Background
involves: C57BL/6N * FVB/NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cyth2tm1c(EUCOMM)Wtsi mutation (0 available); any Cyth2 mutation (21 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• sciatic nerve cells exhibit normal proliferation and apoptosis
• reduced myelin thickness in the sciatic nerve of P5 mice




Genotype
MGI:3836431
cn22
Allelic
Composition
Nfasctm1Bhat/Nfasctm1Bhat
Tg(Mpz-cre)26Mes/?
Genetic
Background
involves: FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nfasctm1Bhat mutation (0 available); any Nfasc mutation (61 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• abnormal neurological defects do not appear until 90 days of age

nervous system
• conduction velocity of tibial/plantar nerves is reduced about 50%




Genotype
MGI:5789297
cn23
Allelic
Composition
Gdap1tm1Ics/Gdap1tm1Ics
Tg(Mpz-cre)26Mes/0
Genetic
Background
involves: FVB/NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gdap1tm1Ics mutation (0 available); any Gdap1 mutation (23 available)
Tg(Mpz-cre)26Mes mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• hypomyelination of the plantar nerve in 19 month old mice with no axonal loss

cellular
N
• axonal area covered by mitochondria in axons of plantar nerves is similar to wild-type mice





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory