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| Nomenclature |
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Symbol:
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Sharpincpdm
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Name:
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SHANK-associated RH domain interacting protein;
chronic proliferative dermatitis
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MGI ID: |
MGI:1856699 |
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Synonyms: |
cpd, cpdm |
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Gene:
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Sharpin
Location:
Chr15:76347040-76351111 bp, - strand
Genetic Position: Chr15,
35.75 cM
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Mutation
origin |
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Strain of Origin:
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C57BL/Ka
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Mutation
description |
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Allele
Type: | |
Spontaneous |
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Mutation: | |
Intragenic deletion |
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Mutation details: A single base pair deletion in the 3' end of exon 1 creates a shift in the open reading frame predicted to cause a premature stop codon at position 624. (J:121810)
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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:14539
HogenEsch H et al.,
"A spontaneous mutation characterized by chronic proliferative dermatitis in C57BL mice."
Am J Pathol 1993 Sep;143(3):972-82
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All: |
21 reference(s)
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Analysis Tools
