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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rettm1Jmi
targeted mutation 1, Jeffrey Milbrandt
MGI:2449909
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Rettm1Jmi/Rettm1Jmi involves: 129X1/SvJ MGI:3623107
ht2
Rettm1Jmi/Ret+ involves: 129X1/SvJ MGI:5585303
cx3
Kifbpem1Hmy/Kifbpem1Hmy
Rettm1Jmi/Rettm1Jmi
involves: 129X1/SvJ MGI:6154378
cx4
Kifbpem1Hmy/Kifbpem1Hmy
Rettm1Jmi/Ret+
involves: 129X1/SvJ MGI:6154379


Genotype
MGI:3623107
hm1
Allelic
Composition
Rettm1Jmi/Rettm1Jmi
Genetic
Background
involves: 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rettm1Jmi mutation (0 available); any Ret mutation (53 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• homozygotes die shortly after birth

cellular
• at E16.5. there is more cell death observed in nulls in the SCG and stellate ganglion than in wild-type
• by E16.5, more proliferating sympathetic neuron precursors are observed in the SCG and STG than in heterozygotes or wild-type

nervous system
• at E16.5. there is more cell death observed in nulls in the SCG and stellate ganglion than in wild-type
• homozygotes lack enteric neurons
• the cervical sympathetic ganglion-like ganglion in nulls are found in a position caudal to the normal SCG location; the position is variable among nulls
• in null embryos, SCG primordia are round-shaped and shorter than in wild-type; at E11.5 there is about a 30% decrease in sympathetic cell number
• in the caudal region of the embryo, sympathetic precursors form clumps and do not distribute properly
• the SCG in nulls display severe but variable reductions in size
• in the prevertebral division, sympathetic ganglia are aberrantly located, reduced in size and display decreased target innervation
• in nulls, sympathetic neurons are variably reduced in size
• there are severe deficits in axonal projections from the SCG; the internal carotid nerve displays aberrant branching and is attenuated on the course of its projection, such that sympathetic fibers in the rostral facial structures are almost entirely depleted
• sympathetic neuron precursors fail to extend long processes; this is apparent in E12.5 embryos in the SCG, STG and prevertebral ganglia
• at E15.5, nerve bundles that form the internal carotid nerve are thin and in some embryos project caudally, not rostrally
• the stellate ganglion displays severe innervation deficits such as attenuation of the vertebral nerve
• the density of esophageal neurons in null mice is only 4% of wild-type neuronal density

digestive/alimentary system
• there is a reduction in density and distribution of symapathetic fibers in the submandibular gland, resulting in absence of sympathetic innervation in the peripheral lobes

endocrine/exocrine glands
• there is a reduction in density and distribution of symapathetic fibers in the submandibular gland, resulting in absence of sympathetic innervation in the peripheral lobes

renal/urinary system
• homozygotes lack kidneys




Genotype
MGI:5585303
ht2
Allelic
Composition
Rettm1Jmi/Ret+
Genetic
Background
involves: 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rettm1Jmi mutation (0 available); any Ret mutation (53 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
renal/urinary system
• analysis of branching at 15.5 dpc revealed a subtle but significant (18%) decrease in ureteric branch tips in Ret+/- embryonic kidneys compared with littermate controls, although other metrics describing the structure of the branched tree were normal
• quantification of cap cells and tip cells per niche also trended toward larger cap and tip volumes (more like younger kidneys), although this did not reach statistical significance
• decreased niche number observed at P0 confirms the tip deficit observed at E15.5




Genotype
MGI:6154378
cx3
Allelic
Composition
Kifbpem1Hmy/Kifbpem1Hmy
Rettm1Jmi/Rettm1Jmi
Genetic
Background
involves: 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kifbpem1Hmy mutation (0 available); any Kifbp mutation (36 available)
Rettm1Jmi mutation (0 available); any Ret mutation (53 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• Tubb3 (Tuj1)-positive vagus nerve fibers absent from stomach in one set of 2 out of 4 E12.5 embryos
• small number of short Tubb3 (Tuj1)-positive vagus nerve fibers on one side of stomach in other set of 2 out of 4 E12.5 embryos
• absence of vagus nerve fibers in vicinity of pancreas of E12.5 embryos




Genotype
MGI:6154379
cx4
Allelic
Composition
Kifbpem1Hmy/Kifbpem1Hmy
Rettm1Jmi/Ret+
Genetic
Background
involves: 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kifbpem1Hmy mutation (0 available); any Kifbp mutation (36 available)
Rettm1Jmi mutation (0 available); any Ret mutation (53 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• delayed colonization of intestines by enteric neural crest-derived cells (ENCCs), as determined by Sox10 staining in E12.5 embryos





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