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

Symbol:	Omgtm1Shmi
Name:	oligodendrocyte myelin glycoprotein; targeted mutation 1, Sha Mi
MGI ID:	MGI:3821628
Synonyms:	OMgp-
Gene:	Omg  Location: Chr11:79391808-79394908 bp, - strand  Genetic Position: Chr11, 46.79 cM, cytoband B5
Alliance:	Omgtm1Shmi page

Germline Transmission:	Earliest citation of germline transmission: J:142129
Parent Cell Line:	v6.5 (ES Cell)
Strain of Origin:	(C57BL/6 x 129S4/SvJae)F1

Allele Type:    Targeted (Null/knockout, Reporter) Mutations:    Insertion, Intragenic deletion   Mutation details: The coding region was replaced by a GFP and neo cassette. The absence of protein expression was confirmed by western blot on brain and spinal cord extracts. (J:142129)

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 Omg Mutation:	20 strains or lines available

Original:	J:142129 Ji B, et al., Assessment of functional recovery and axonal sprouting in oligodendrocyte-myelin glycoprotein (OMgp) null mice after spinal cord injury. Mol Cell Neurosci. 2008 Oct;39(2):258-67
All:	6 reference(s)