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Myoctm1.1Rjo
Targeted Allele Detail
Summary
Symbol: Myoctm1.1Rjo
Name: myocilin; targeted mutation 1.1, Randy L Johnson
MGI ID: MGI:2183812
Gene: Myoc  Location: Chr1:162466724-162477262 bp, + strand  Genetic Position: Chr1, 70.29 cM
Alliance: Myoctm1.1Rjo page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:72628
Parent Cell Line:  AB1 (ES Cell)
Strain of Origin:  129S7/SvEvBrd-Hprt1+
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutation:    Intragenic deletion
 
Mutation detailsThe mutant is derived from Myoctm1Rjo where the floxed neo cassette has been removed by crossing to a cre-expressing mouse line. The absence of gene expression in eyes of homozygous mutant animals was confirmed by Western blot analysis and RT-PCR. (J:72628)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Myoc Mutation:  27 strains or lines available
References
Original:  J:72628 Kim BS, et al., Targeted Disruption of the Myocilin Gene (Myoc) Suggests that Human Glaucoma-Causing Mutations Are Gain of Function. Mol Cell Biol. 2001 Nov;21(22):7707-13
All:  7 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
04/23/2024
MGI 6.23
The Jackson Laboratory