Summary | Mutation origin | Mutation description | Phenotypes | Find Mice (IMSR) | References

Symbol:	Snrpntm5Alb
Name:	small nuclear ribonucleoprotein N; targeted mutation 5, Arthur L Beaudet
MGI ID:	MGI:3617407
Gene:	Snrpn  Location: Chr7:59632243-59789967 bp, - strand  Genetic Position: Chr7, 34.04 cM
Alliance:	Snrpntm5Alb page

Germline Transmission:	Earliest citation of germline transmission: J:105289
Parent Cell Line:	AB2.2 (ES Cell)
Strain of Origin:	129S7/SvEvBrd-Hprt1b-m2

Allele Type:    Targeted (Null/knockout) Mutations:    Insertion, Intragenic deletion   Mutation details: ES cells containing Rr70 were targeted with a second vector, inserting a loxP site and exons 1-2 of the Hprt minigene 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)

View phenotypes and curated references for all genotypes (concatenated display).

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:	23 strains or lines available

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)