Ngftm1.1(NGF*)Cat
Targeted Allele Detail
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| Symbol: |
Ngftm1.1(NGF*)Cat |
| Name: |
nerve growth factor; targeted mutation 1.1, Antonio Cattaneo |
| MGI ID: |
MGI:8314973 |
| Gene: |
Ngf Location: Chr3:102377235-102428329 bp, + strand Genetic Position: Chr3, 45.25 cM
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| Alliance: |
Ngftm1.1(NGF*)Cat page
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| Allele Type: |
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Targeted (Humanized sequence, Inserted expressed sequence, Null/knockout) |
| Mutations: |
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Insertion, Intragenic deletion
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Mutation details:
The human NGF coding sequence with an arginine to tryptophan substitution at codon 100 (p.R100W) and loxP site flanked NeoR/KanR cassette and PGK promoter replaced the mouse Ngf coding sequence via homologous recombination. The neo/kana cassette was removed through subsequent Cre-mediated recombination. The C-to-T transition at position 661 resulting in the p.R100W mutation is seen in patients with Hereditary Sensory and Autonomic Neuropathy type 5 (HSAN5).
(J:282017)
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| Original: |
J:282017 Testa G, et al., The NGF(R100W) Mutation Specifically Impairs Nociception without Affecting Cognitive Performance in a Mouse Model of Hereditary Sensory and Autonomic Neuropathy Type V. J Neurosci. 2019 Dec 4;39(49):9702-9715 |
| All: |
1 reference(s) |
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