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Phenotypes Associated with This Genotype
Genotype
MGI:6388458
Allelic
Composition
Ngftm1(NGF*)Cat/Ngf+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ngftm1(NGF*)Cat mutation (0 available); any Ngf mutation (12 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• mice show no learning or memory deficits in the Morris water maze, in the object recognition test, in exploratory activity and preference index
• a non-noxious stimulus (small piece of tape applied to the back) takes more time to induce a removal reaction than in controls at 6 months of age, but not at 2 months, indicating that mice are less sensitive to somatosensory inputs
• however, response to gentle stroking of the glabrous skin is normal
• chemical nociception induced by capsaicin injection in the hindpaw is impaired at 2 months and 6 months of age
• thermal nociception is normal at 2 month of age but decreases by 6 months of age, with adults showing a higher latency to respond to high-temperature stimulus
• cold sensitivity, measured by topical acetone application on the hindpaw, is reduced at 2 and 6 months of age

nervous system
N
• mice show normal numbers of DRG neurons at P5, 2 months, and 6 months, normal numbers of SCG, normal density of ChAT+ neurons in the medial septum and striatum, normal conduction velocities of the 3 main sensory fiber populations, ABeta, Adelta, and C fibers, and normal Schaffer collateral-CA1 long-term potentiation
• mice show a reduction in hairy and glabrous (sensory fibers) skin sensory innervation at 6 months of age, but not at 2 months
• however, mice show normal sympathetic innervation of key target organs such as the heart, stomach, kidney, spleen
• cross-sectional area of the sciatic nerve is decreased
• sciatic nerve shows a decrease in the number of nonmyelinated axons
• however, the number of myelinated axons in the sciatic nerve is unaffected

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
hereditary sensory and autonomic neuropathy type 5 DOID:0070145 OMIM:608654
J:282017


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory