All Phenotypes Rab3d<tm1Rja> MGI Mouse

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Phenotypes associated with this allele

Allele Symbol
Allele Name
Allele ID

Rab3d^tm1Rja
targeted mutation 1, Reinhard Jahn
MGI:2669989

Summary

11 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Rab3d^tm1Rja/Rab3d^tm1Rja	involves: 129P2/OlaHsd	MGI:3625937
cx2	Rab3a^tm1Sud/Rab3a^tm1Sud Rab3d^tm1Rja/Rab3d^tm1Rja	involves: 129 * 129P2/OlaHsd	MGI:3625943
cx3	Rab3a^tm1Sud/Rab3a⁺ Rab3b^tm1Sud/Rab3b^tm1Sud Rab3c^tm1Sud/Rab3c^tm1Sud Rab3d^tm1Rja/Rab3d^tm1Rja	involves: 129 * 129P2/OlaHsd	MGI:3625945
cx4	Rab3a^tm1Sud/Rab3a^tm1Sud Rab3b^tm1Sud/Rab3b^tm1Sud Rab3d^tm1Rja/Rab3d^tm1Rja	involves: 129 * 129P2/OlaHsd	MGI:3625947
cx5	Rab3a^tm1Sud/Rab3a^tm1Sud Rab3b^tm1Sud/Rab3b⁺ Rab3c^tm1Sud/Rab3c^tm1Sud Rab3d^tm1Rja/Rab3d^tm1Rja	involves: 129 * 129P2/OlaHsd	MGI:3625948
cx6	Rab3a^tm1Sud/Rab3a^tm1Sud Rab3b^tm1Sud/Rab3b^tm1Sud Rab3c^tm1Sud/Rab3c⁺ Rab3d^tm1Rja/Rab3d^tm1Rja	involves: 129 * 129P2/OlaHsd	MGI:3625949
cx7	Rab3a^tm1Sud/Rab3a^tm1Sud Rab3b^tm1Sud/Rab3b^tm1Sud Rab3c^tm1Sud/Rab3c^tm1Sud Rab3d^tm1Rja/Rab3d⁺	involves: 129 * 129P2/OlaHsd	MGI:3625950
cx8	Rab3a^tm1Sud/Rab3a^tm1Sud Rab3b^tm1Sud/Rab3b^tm1Sud Rab3c^tm1Sud/Rab3c^tm1Sud Rab3d^tm1Rja/Rab3d^tm1Rja	involves: 129 * 129P2/OlaHsd	MGI:3625951
cx9	Rab3a^tm1Sud/Rab3a^tm1Sud Rab3c^tm1Sud/Rab3c^tm1Sud Rab3d^tm1Rja/Rab3d^tm1Rja	involves: 129 * 129P2/OlaHsd	MGI:3625965
cx10	Rab3b^tm1Sud/Rab3b^tm1Sud Rab3d^tm1Rja/Rab3d^tm1Rja	involves: 129P2/OlaHsd	MGI:3625942
cx11	Rab3b^tm1Sud/Rab3b^tm1Sud Rab3c^tm1Sud/Rab3c^tm1Sud Rab3d^tm1Rja/Rab3d^tm1Rja	involves: 129P2/OlaHsd	MGI:3625944

Allelic Composition	Rab3d^tm1Rja/Rab3d^tm1Rja
Genetic Background	involves: 129P2/OlaHsd

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rab3d^tm1Rja mutation (1 available); any Rab3d mutation (18 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

normal phenotype

no abnormal phenotype detected ( J:105478 )

Allelic Composition	Rab3a^tm1Sud/Rab3a^tm1Sud Rab3d^tm1Rja/Rab3d^tm1Rja
Genetic Background	involves: 129 * 129P2/OlaHsd

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rab3a^tm1Sud mutation (2 available); any Rab3a mutation (15 available)
Rab3d^tm1Rja mutation (1 available); any Rab3d mutation (18 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

normal phenotype

no abnormal phenotype detected ( J:105478 )

Allelic Composition	Rab3a^tm1Sud/Rab3a⁺ Rab3b^tm1Sud/Rab3b^tm1Sud Rab3c^tm1Sud/Rab3c^tm1Sud Rab3d^tm1Rja/Rab3d^tm1Rja
Genetic Background	involves: 129 * 129P2/OlaHsd

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rab3a^tm1Sud mutation (2 available); any Rab3a mutation (15 available)
Rab3b^tm1Sud mutation (1 available); any Rab3b mutation (12 available)
Rab3c^tm1Sud mutation (1 available); any Rab3c mutation (21 available)
Rab3d^tm1Rja mutation (1 available); any Rab3d mutation (18 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

normal phenotype

no abnormal phenotype detected ( J:105478 )

Allelic Composition	Rab3a^tm1Sud/Rab3a^tm1Sud Rab3b^tm1Sud/Rab3b^tm1Sud Rab3d^tm1Rja/Rab3d^tm1Rja
Genetic Background	involves: 129 * 129P2/OlaHsd

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rab3a^tm1Sud mutation (2 available); any Rab3a mutation (15 available)
Rab3b^tm1Sud mutation (1 available); any Rab3b mutation (12 available)
Rab3d^tm1Rja mutation (1 available); any Rab3d mutation (18 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

growth/size/body

decreased body weight ( J:105478 )

• male and female triple knockouts which are deficient for Rab3a display a weight decrease at 5 weeks of age

behavior/neurological

abnormal behavior ( J:105478 )

• surviving triple knockouts exhibit abnormal cage behavior and are unable to mate (no details provided)

respiratory system

respiratory distress ( J:105478 )

• triple knockouts lacking Rab3a show respiratory impairment similar to, but less severe than that shown by quadruple knockouts

Allelic Composition	Rab3a^tm1Sud/Rab3a^tm1Sud Rab3b^tm1Sud/Rab3b⁺ Rab3c^tm1Sud/Rab3c^tm1Sud Rab3d^tm1Rja/Rab3d^tm1Rja
Genetic Background	involves: 129 * 129P2/OlaHsd

Find Mice

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

mortality/aging

neonatal lethality, incomplete penetrance ( J:105478 )

• 50% of triple Rab3 knockouts with one copy of Rab3c survive

growth/size/body

decreased body weight ( J:105478 )

• male and female triple knockouts which are deficient for Rab3a and heterozygous for Rab3b display a weight decrease at 5 weeks of age

respiratory system

respiratory distress ( J:105478 )

• triple knockouts lacking Rab3a show respiratory impairment similar to, but less severe than that shown by quadruple knockouts

Allelic Composition	Rab3a^tm1Sud/Rab3a^tm1Sud Rab3b^tm1Sud/Rab3b^tm1Sud Rab3c^tm1Sud/Rab3c⁺ Rab3d^tm1Rja/Rab3d^tm1Rja
Genetic Background	involves: 129 * 129P2/OlaHsd

Find Mice

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

mortality/aging

neonatal lethality, incomplete penetrance ( J:105478 )

• 50% of triple Rab3 knockouts that are heterozygous for Rab3c survive

growth/size/body

decreased body weight ( J:105478 )

• male and female triple knockouts which are deficient for Rab3a and heterozygous for Rab3c display a weight decrease at 5 weeks of age

Allelic Composition	Rab3a^tm1Sud/Rab3a^tm1Sud Rab3b^tm1Sud/Rab3b^tm1Sud Rab3c^tm1Sud/Rab3c^tm1Sud Rab3d^tm1Rja/Rab3d⁺
Genetic Background	involves: 129 * 129P2/OlaHsd

Find Mice

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

mortality/aging

neonatal lethality ( J:105478 )

Allelic Composition	Rab3a^tm1Sud/Rab3a^tm1Sud Rab3b^tm1Sud/Rab3b^tm1Sud Rab3c^tm1Sud/Rab3c^tm1Sud Rab3d^tm1Rja/Rab3d^tm1Rja
Genetic Background	involves: 129 * 129P2/OlaHsd

Find Mice

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

mortality/aging

neonatal lethality, complete penetrance ( J:105478 )

• quadruple knockouts are born alive and react to stimuli; pups do not have milk in their stomachs and die soon after birth due to respiratory distress

homeostasis/metabolism

cyanosis ( J:105478 )

• newborn mice are cyanotic

nervous system

abnormal CNS synaptic transmission ( J:104983 )

• synaptic response (release) in presence of high calcium is potentiated in knockout neurons compared to control

abnormal excitatory postsynaptic currents ( J:104983 , J:105478 )

• repetitive stimulation of cultured quadruple knockout neurons induces strong initial facilitation; after ~5 synaptic responses, converged to similar amplitudes with controls (J:104983)

• EPSCs recover faster in mutant neurons than in control after depletion of the pool of synaptic vesicles (J:104983)

• EPSCs induced by action potentials are 30% smaller than in control (Rab3b,c,d triple knockout) animals; Rab3a deficient mice show no decline in EPSC indicating that lack of this isoform is not the sole reason for the decrease observed in quadruple knockouts (J:105478)

decreased neurotransmitter release ( J:105478 )

• in neurons, the synaptic release probability of vesicles is reduced by 40% compared to control triple knockout neurons; Rab3a-deficient neurons displayed no difference in release probability from wild-type

enhanced paired-pulse facilitation ( J:104983 )

• neurons show strong paired-pulse facilitation

respiratory system

abnormal breathing pattern ( J:105478 )

• newborn mice exhibit shallow and irregular breathing patterns

respiratory distress ( J:105478 )

• newborn mice exhibit respiratory distress and die soon after birth; if mice are placed in a high oxygen atmosphere, survival time is increased

Allelic Composition	Rab3a^tm1Sud/Rab3a^tm1Sud Rab3c^tm1Sud/Rab3c^tm1Sud Rab3d^tm1Rja/Rab3d^tm1Rja
Genetic Background	involves: 129 * 129P2/OlaHsd

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rab3a^tm1Sud mutation (2 available); any Rab3a mutation (15 available)
Rab3c^tm1Sud mutation (1 available); any Rab3c mutation (21 available)
Rab3d^tm1Rja mutation (1 available); any Rab3d mutation (18 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

mortality/aging

neonatal lethality, incomplete penetrance ( J:105478 )

• less than 100% of triple knockouts survive

growth/size/body

decreased body weight ( J:105478 )

• male and female triple knockouts which are deficient for Rab3a display a weight decrease at 5 weeks of age

behavior/neurological

abnormal behavior ( J:105478 )

• surviving triple knockouts exhibit abnormal cage behavior and are unable to mate (no details provided)

Allelic Composition	Rab3b^tm1Sud/Rab3b^tm1Sud Rab3d^tm1Rja/Rab3d^tm1Rja
Genetic Background	involves: 129P2/OlaHsd

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rab3b^tm1Sud mutation (1 available); any Rab3b mutation (12 available)
Rab3d^tm1Rja mutation (1 available); any Rab3d mutation (18 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

normal phenotype

no abnormal phenotype detected ( J:105478 )

Allelic Composition	Rab3b^tm1Sud/Rab3b^tm1Sud Rab3c^tm1Sud/Rab3c^tm1Sud Rab3d^tm1Rja/Rab3d^tm1Rja
Genetic Background	involves: 129P2/OlaHsd

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rab3b^tm1Sud mutation (1 available); any Rab3b mutation (12 available)
Rab3c^tm1Sud mutation (1 available); any Rab3c mutation (21 available)
Rab3d^tm1Rja mutation (1 available); any Rab3d mutation (18 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

normal phenotype

no abnormal phenotype detected ( J:105478 )

• triple knockouts are fully viable; mating and growth defects seen in other triple knockouts are rescued by presence of wild-type Rab3a allele

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