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

Symbol:	Gcm1tm1Jcc
Name:	glial cells missing homolog 1; targeted mutation 1, James C Cross
MGI ID:	MGI:2183479
Synonyms:	Gcm1-
Gene:	Gcm1  Location: Chr9:77959240-77972906 bp, + strand  Genetic Position: Chr9, 43.49 cM, cytoband E1-E3
Alliance:	Gcm1tm1Jcc page

Germline Transmission:	Earliest citation of germline transmission: J:63123
Parent Cell Line:	R1 (ES Cell)
Strain of Origin:	(129X1/SvJ x 129S1/Sv)F1-Kitl+

Allele Type:    Targeted (Null/knockout, Reporter) Mutations:    Insertion, Intragenic deletion   Mutation details: Sequence upstream of the start codon in exon 2 through intron 5 was replaced with a cassette containing lacZ and neo. (J:63123)

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

In Mice Carrying this Mutation:	27 assay results
In Structures Affected by this Mutation:	4 anatomical structure(s)

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 Gcm1 Mutation:	23 strains or lines available

Original:	J:63123 Anson-Cartwright L, et al., The glial cells missing-1 protein is essential for branching morphogenesis in the chorioallantoic placenta. Nat Genet. 2000 Jul;25(3):311-4
All:	6 reference(s)