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Svep1em1Nost
Endonuclease-mediated Allele Detail
Summary
Symbol: Svep1em1Nost
Name: sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1; endonuclease-mediated mutation 1, Nathan O Stitziel
MGI ID: MGI:7516157
Synonyms: Svep12699G, SvepG
Gene: Svep1  Location: Chr4:58042796-58206596 bp, - strand  Genetic Position: Chr4, 31.87 cM, cytoband B-C2
Alliance: Svep1em1Nost page
Mutation
origin
Strain of Origin:  C57BL/6
Mutation
description
Allele Type:    Endonuclease-mediated (Humanized sequence)
Mutation:    Single point mutation
 
Mutation detailsAspartic acid codon 2699 (GAT) in exon 38 was changed to glycine (GGT) (p.D2699G) using an sgRNA and an ssODN template with CRISPR/Cas9 technology. The mutation is the equivalent of the human p.D2702G mutation associated with coronary artery disease (CAD). (J:304349)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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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 Svep1 Mutation:  169 strains or lines available
References
Original:  J:304349 Jung IH, et al., SVEP1 is a human coronary artery disease locus that promotes atherosclerosis. Sci Transl Med. 2021 Mar 24;13(586)
All:  1 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