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| Nomenclature |
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Symbol:
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Kcnq2Nmf134
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Name:
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potassium voltage-gated channel, subfamily Q, member 2;
neuroscience mutagenesis facility, 134
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MGI ID: |
MGI:2661797 |
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Synonyms: |
Kcnq2V182M |
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Gene:
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Kcnq2
Location:
Chr2:181075579-181135291 bp, - strand
Genetic Position: Chr2,
103.57 cM, cytoband H3-4
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Mutation
origin |
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Strain of Origin:
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C57BL/6J
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Mutation
description |
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Allele
Type: | |
Chemically induced (ENU) |
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Mutation: | |
Single point mutation |
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Mutation details: A G-to-T transversion mutation in codon 182 results in the substitution of methionine for valine at this highly conserved position in the encoded protein. (J:136510)
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Inheritance: | |
Semidominant |
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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Disease models
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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| References |
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Original: |
J:82238
JAX Neuroscience Mutagenesis Facility,
"Heritable mouse mutants from JAX NMF ENU Mutagenesis Program"
MGI Direct Data Submission 2003;():
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All: |
3 reference(s)
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Analysis Tools
