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| Nomenclature |
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Symbol:
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Pstpip2cmo
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Name:
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proline-serine-threonine phosphatase-interacting protein 2;
chronic multifocal osteomyelitis
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MGI ID: |
MGI:1856595 |
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Synonyms: |
cmo |
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Gene:
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Pstpip2
Location:
Chr18:77794545-77882007 bp, + strand
Genetic Position: Chr18,
52.38 cM, cytoband E3
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Mutation
origin |
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Strain of Origin:
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C.D2-Qa2
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Mutation
description |
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Allele
Type: | |
Spontaneous |
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Mutation: | |
Single point mutation |
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Mutation details: Sequncing revealed a T to C transversion at nt position 293 that resulted in a highly conserved leucine to be replaced by a proline at amino acid position 98. (J:104476)
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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:1534
Byrd L et al.,
"Chronic multifocal osteomyelitis, a new recessive mutation on chromosome 18 of the mouse."
Genomics 1991 Dec;11(4):794-8
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All: |
5 reference(s)
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Analysis Tools
