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Ptpn6me-B2
Spontaneous Allele Detail
Summary
Symbol: Ptpn6me-B2
Name: protein tyrosine phosphatase, non-receptor type 6; motheaten B2
MGI ID: MGI:4947257
Synonyms: Ptpn6meB2
Gene: Ptpn6  Location: Chr6:124697670-124715672 bp, - strand  Genetic Position: Chr6, 59.17 cM
Alliance: Ptpn6me-B2 page
Mutation
origin
Strain of Origin:  BALB/c
Mutation
description
Allele Type:    Spontaneous
Mutation:    Viral insertion
 
Mutation detailsThe B2 element (247 bp) was inserted into exon 6 with a 16 bp duplication that results in alternative splicing and amino acid substitution. (J:169850)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 6 anatomical structure(s)
Find Mice (IMSR)
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
Carrying any Ptpn6 Mutation:  47 strains or lines available
References
Original:  J:169850 Nesterovitch AB, et al., Spontaneous insertion of a b2 element in the ptpn6 gene drives a systemic autoinflammatory disease in mice resembling neutrophilic dermatosis in humans. Am J Pathol. 2011 Apr;178(4):1701-14
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory