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Puratm1Herm
Targeted Allele Detail
Summary
Symbol: Puratm1Herm
Name: purine rich element binding protein A; targeted mutation 1, Jochen Herms
MGI ID: MGI:5305287
Gene: Pura  Location: Chr18:36414150-36425588 bp, + strand  Genetic Position: Chr18, 19.46 cM, cytoband B3
Alliance: Puratm1Herm page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:179606
Parent Cell Line:  E14 (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
    The open reading frame was replaced with a neo cassette. (J:179606)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 4 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 Pura Mutation:  26 strains or lines available
References
Original:  J:179606 Hokkanen S, et al., Lack of Pur-alpha alters postnatal brain development and causes megalencephaly. Hum Mol Genet. 2012 Feb 1;21(3):473-84
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
06/12/2024
MGI 6.13
The Jackson Laboratory