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Megf8m687Ddg
Chemically induced Allele Detail
Summary
Symbol: Megf8m687Ddg
Name: multiple EGF-like-domains 8; mutation 687, David D Ginty
MGI ID: MGI:4455205
Synonyms: Megf8L1775P
Gene: Megf8  Location: Chr7:25016589-25065342 bp, + strand  Genetic Position: Chr7, 13.75 cM
Alliance: Megf8m687Ddg page
Mutation
origin
Strain of Origin:  C57BL/6
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced a T to C point mutation that results in the amino acid substitution of proline for lysine at position 1775 (L1775P) in the fourth Kelch domain. (J:206541)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 3 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: 1 strain available      Cell Lines: 0 lines available
Carrying any Megf8 Mutation:  96 strains or lines available
References
Original:  J:159834 Merte J, et al., A forward genetic screen in mice identifies Sema3A(K108N), which binds to neuropilin-1 but cannot signal. J Neurosci. 2010 Apr 21;30(16):5767-75
All:  2 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
04/16/2024
MGI 6.23
The Jackson Laboratory