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

Symbol:	Del(19Htr7-Mphosph1)2Hgc
Name:	deletion, Chr 19, Human Genome Center 2
MGI ID:	MGI:3487279
Synonyms:	Del(19Htr7-Kif20b)2Hgc, Del2Hgc, DelMMU19
Gene:	Del(19Htr7-Mphosph1)2Hgc  Location: unknown  Genetic Position: Chr19, Syntenic

Germline Transmission:	Earliest citation of germline transmission: J:93237
Parent Cell Line:	ESVJ (ES Cell)
Strain of Origin:	129X1/SvJ

Allele Type:    Targeted (Null/knockout) Mutations:    Intergenic deletion, Intragenic deletion   Del(19Htr7-Mphosph1)2Hgc involves 7 genes/genome features (Gm22853, Gm23075, Mir1950 ...) View all   Mutation details: Cre-mediated recombination resulted in the deletion of a 845 kb segment extending distally from Htr7 to Mphosph1, with breakpoint coordinates 35,033 and 35,878 from NCBI mouse build 32. (J:93237)

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 Del(19Htr7-Mphosph1)2Hgc Mutation:	0 strains or lines available

Original:	J:93237 Nobrega MA, et al., Megabase deletions of gene deserts result in viable mice. Nature. 2004 Oct 21;431(7011):988-93
All:	1 reference(s)