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| Nomenclature |
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Symbol:
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Pla2g6m1J
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Name:
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phospholipase A2, group VI;
mutation 1 Jackson
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MGI ID: |
MGI:4412026 |
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Gene:
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Pla2g6
Location:
Chr15:79286228-79328390 bp, - strand
Genetic Position: Chr15,
37.7 cM
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Mutation
origin |
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Strain of Origin:
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C3H/HeJ
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Mutation
description |
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Allele
Type: | |
Spontaneous |
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Mutation: | |
Viral insertion |
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Mutation details: A viral insertion occurred spontaneously in intron 1 upstream of the start codon, resulting in a dramatic reduction of trasncript levels. (J:183152)
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Inheritance: | |
Recessive |
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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:183152
Strokin M et al.,
"Severe disturbance in the Ca2+ signaling in astrocytes from mouse models of human infantile neuroaxonal dystrophy with mutated Pla2g6."
Hum Mol Genet 2012 Apr 4;():
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All: |
1 reference(s)
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Analysis Tools
