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Gcm1tm1Jcc
Targeted Allele Detail
Summary
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
Mutation
origin
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+
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsSequence upstream of the start codon in exon 2 through intron 5 was replaced with a cassette containing lacZ and neo. (J:63123)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 27 assay results
In Structures Affected by this Mutation: 4 anatomical structure(s)
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 Gcm1 Mutation:  23 strains or lines available
Notes
Phenotypic Similarity to Human Syndrome: Preeclampsia/Eclampsia (induced by fetus J:185528)
References
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)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory