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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Nxf1Mvb1
modifier of vibrator 1
MGI:2680965
Summary 10 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Nxf1Mvb1/Nxf1Mvb1 involves: C3H/HeJ * C57BL/6J * CAST/Ei MGI:3722670
cx2
Nxf1Mvb1/Nxf1Mvb1
Pitpnavb/Pitpnavb
involves: C3HeB/Fe * C57BL/6J * CAST/Ei * DBA/2J MGI:3719467
cx3
Eya1bor/Eya1bor
Nxf1Mvb1/Nxf1+
involves: C3HeB/FeJ * C57BL/6J * CAST/Ei MGI:3719482
cx4
Eya1bor/Eya1bor
Nxf1Mvb1/Nxf1Mvb1
involves: C3HeB/FeJ * C57BL/6J * CAST/Ei MGI:3719480
cx5
Ap3d1mh-2J/Ap3d1mh-2J
Nxf1Mvb1/Nxf1Mvb1
involves: C3H/HeJ * C57BL/6 MGI:3848524
cx6
Atcayji-hes/Atcayji-hes
Nxf1Mvb1/Nxf1Mvb1
involves: C3H/HeJ * C57BL/6 MGI:3848526
cx7
Nxf1Mvb1/Nxf1Mvb1
Usp14ax-J/Usp14ax-J
involves: C57BL/6 MGI:3848536
cx8
Nxf1em1Haml/Nxf1Mvb1
Pitpnavb/Pitpnavb
involves: C57BL/6 * DBA/2J MGI:5629975
cx9
Nxf1Mvb1/Nxf1Mvb1
Pitpnavb/Pitpnavb
involves: C57BL/6J * CAST/Ei * DBA/2J MGI:3722644
cx10
Nxf1Mvb1/Nxf1+
Pitpnavb/Pitpnavb
involves: C57BL/6J * CAST/Ei * DBA/2J MGI:3722646


Genotype
MGI:3722670
hm1
Allelic
Composition
Nxf1Mvb1/Nxf1Mvb1
Genetic
Background
involves: C3H/HeJ * C57BL/6J * CAST/Ei
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nxf1Mvb1 mutation (1 available); any Nxf1 mutation (36 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• more Nxf1Mvb1-CAST/Ei homozygotes are generated from a cross betwen Eya1bor and Nxf1Mvb1-CAST/Ei mice than non-Nxf1Mvb1-CAST/Ei homozygotes




Genotype
MGI:3719467
cx2
Allelic
Composition
Nxf1Mvb1/Nxf1Mvb1
Pitpnavb/Pitpnavb
Genetic
Background
involves: C3HeB/Fe * C57BL/6J * CAST/Ei * DBA/2J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nxf1Mvb1 mutation (1 available); any Nxf1 mutation (36 available)
Pitpnavb mutation (1 available); any Pitpna mutation (37 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• only mild tremors are observed

nervous system
N
• no abnormalities are detected in the brains stem or spinal cord




Genotype
MGI:3719482
cx3
Allelic
Composition
Eya1bor/Eya1bor
Nxf1Mvb1/Nxf1+
Genetic
Background
involves: C3HeB/FeJ * C57BL/6J * CAST/Ei
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eya1bor mutation (2 available); any Eya1 mutation (56 available)
Nxf1Mvb1 mutation (1 available); any Nxf1 mutation (36 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• the auditory brainstem threshold is increased compared to wild-type mice but intermediate between Eya1bor Nxf1Mvb1-C57BL/6J and Eya1bor Nxf1Mvb1-CAST/Ei homozygotes




Genotype
MGI:3719480
cx4
Allelic
Composition
Eya1bor/Eya1bor
Nxf1Mvb1/Nxf1Mvb1
Genetic
Background
involves: C3HeB/FeJ * C57BL/6J * CAST/Ei
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Eya1bor mutation (2 available); any Eya1 mutation (56 available)
Nxf1Mvb1 mutation (1 available); any Nxf1 mutation (36 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• mice exhibit less noticeable head bobbing compared to Eya1bor Nxf1Mvb1-C57BL/6J homozygotes
• mice exhibit less noticeable circling compared to Eya1bor Nxf1Mvb1-C57BL/6J homozygotes

hearing/vestibular/ear
• the auditory brainstem threshold is increased compared to wild-type mice but less than that of Eya1bor Nxf1Mvb1-C57BL/6J homozygotes

nervous system
• 6 of 12 mice have a loss of spiral ganglion cells in the apical turn of the cochlea
• 3 of 12 mice have more severe phenotypes

renal/urinary system
N
• mice do not exhibit kidney defects or associated mortality as in Eya1bor homozygotes




Genotype
MGI:3848524
cx5
Allelic
Composition
Ap3d1mh-2J/Ap3d1mh-2J
Nxf1Mvb1/Nxf1Mvb1
Genetic
Background
involves: C3H/HeJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ap3d1mh-2J mutation (1 available); any Ap3d1 mutation (79 available)
Nxf1Mvb1 mutation (1 available); any Nxf1 mutation (36 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Ap3d1mh-2J/Ap3d1mh-2J coat color dilution is attenuated in Ap3d1mh-2J/Ap3d1mh-2J Nxf1Mvb1/Nxf1Mvb1 mice

pigmentation
• normalization of pigmentation relative to Ap3d1mh-2J single homozygotes

behavior/neurological
• reduced tremors relative to Ap3d1mh-2J single homozygotes

integument
• normalization of pigmentation relative to Ap3d1mh-2J single homozygotes




Genotype
MGI:3848526
cx6
Allelic
Composition
Atcayji-hes/Atcayji-hes
Nxf1Mvb1/Nxf1Mvb1
Genetic
Background
involves: C3H/HeJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Atcayji-hes mutation (1 available); any Atcay mutation (27 available)
Nxf1Mvb1 mutation (1 available); any Nxf1 mutation (36 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• reduced ataxia relative to Ap3d1mh-2J single homozygotes
• elimination of the tendency to jump out of open fields in behavior tests displayed by Ap3d1mh-2J single homozygotes




Genotype
MGI:3848536
cx7
Allelic
Composition
Nxf1Mvb1/Nxf1Mvb1
Usp14ax-J/Usp14ax-J
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nxf1Mvb1 mutation (1 available); any Nxf1 mutation (36 available)
Usp14ax-J mutation (1 available); any Usp14 mutation (47 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• reduced amplitude of tremors relative to those of Usp14ax-J singlle homozygotes




Genotype
MGI:5629975
cx8
Allelic
Composition
Nxf1em1Haml/Nxf1Mvb1
Pitpnavb/Pitpnavb
Genetic
Background
involves: C57BL/6 * DBA/2J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nxf1em1Haml mutation (1 available); any Nxf1 mutation (36 available)
Nxf1Mvb1 mutation (1 available); any Nxf1 mutation (36 available)
Pitpnavb mutation (1 available); any Pitpna mutation (37 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• improved survival compared with Nxf1Mvb1-C57BL/6J/Nxf1Mvb1-CAST/Ei Pitpnavb/Pitpnavb mice

behavior/neurological
• reduced tremor score compared with Nxf1Mvb1-C57BL/6J/Nxf1Mvb1-CAST/Ei Pitpnavb/Pitpnavb mice




Genotype
MGI:3722644
cx9
Allelic
Composition
Nxf1Mvb1/Nxf1Mvb1
Pitpnavb/Pitpnavb
Genetic
Background
involves: C57BL/6J * CAST/Ei * DBA/2J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nxf1Mvb1 mutation (1 available); any Nxf1 mutation (36 available)
Pitpnavb mutation (1 available); any Pitpna mutation (37 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• lethality observed in Pitpnavb mice is suppressed with mice living past 750 days compared to less than 100 days in Pitnavb homozygotes

nervous system
• fewer neurons with pathologies were observed than in Pitpnavb/Pitpnavb Nxf1Mvb1-CAST/Ei/Nxf1Mvb1-C57BL/6J mice




Genotype
MGI:3722646
cx10
Allelic
Composition
Nxf1Mvb1/Nxf1+
Pitpnavb/Pitpnavb
Genetic
Background
involves: C57BL/6J * CAST/Ei * DBA/2J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nxf1Mvb1 mutation (1 available); any Nxf1 mutation (36 available)
Pitpnavb mutation (1 available); any Pitpna mutation (37 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• lethality observed in Pitpnavb mice is suppressed with mice living past 500 days compared to less than 100 days in Pitnavb homozygotes and more than 750 days in Pitnavb Nxf1mvb1-CAST/Ei homozygotes





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory