Ptprcnim
Chemically induced Allele Detail
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Symbol: |
Ptprcnim |
Name: |
protein tyrosine phosphatase receptor type C; nimbus |
MGI ID: |
MGI:5694925 |
Gene: |
Ptprc Location: Chr1:137990599-138103446 bp, - strand Genetic Position: Chr1, 60.73 cM
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Alliance: |
Ptprcnim page
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Strain of Origin: |
C57BL/6JAnu
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Project Collection: |
APF ENU Mutagenesis
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Allele Type: |
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Chemically induced (ENU) (Null/knockout) |
Mutation: |
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Single point mutation
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Mutation details: ENU mutagenesis induced a C to T point mutation upstream of exon 18 which introduces an introgenic 1 G nucleotide of the sonsensus splice acceptor sequence. The altered splice acceptor results in a frameshift and truncation at exon 18. Flow cytometry confirmed the absence of protein expression on the surface of B lymphocytes.
(J:225105)
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View phenotypes and curated references for all genotypes (concatenated display).
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Mouse strains and cell lines
available from the International Mouse Strain Resource
(IMSR) |
Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available
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Carrying any Ptprc Mutation: |
190 strains or lines available
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Original: |
J:225105 Andrews TD, et al., Massively parallel sequencing of the mouse exome to accurately identify rare, induced mutations: an immediate source for thousands of new mouse models. Open Biol. 2012 May;2(5):120061 |
All: |
1 reference(s) |
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