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Snrpntm5Alb
Targeted Allele Detail
Nomenclature
Symbol: Snrpntm5Alb
Name: small nuclear ribonucleoprotein N; targeted mutation 5, Arthur L Beaudet
MGI ID: MGI:3617407
Gene: Snrpn  Location: Chr7:59982495-60005111 bp, - strand  Genetic Position: Chr7, 34.04 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:105289
Parent Cell Line:  AB2.2 (ES Cell)
Strain of Origin:  129S7/SvEvBrd-Hprtb-m2
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsES cells containing Snrpntm4Alb were targeted with a second vector containing another loxP site and exons 1-2 of the Hprt minigene located at the distal end of the BAC, about 93 kb upstream of exon 1. Transient expression of cre recombinase resulted in the excision of the 80 kb sequence between the two loxP sites. (J:105289)
Phenotypes
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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 Snrpn Mutation:  13 strains or lines available
References
Original:  J:105289 Wu MY, et al., Mouse imprinting defect mutations that model Angelman syndrome. Genesis. 2006 Jan;44(1):12-22
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/22/2016
MGI 6.06
The Jackson Laboratory