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S100a16em1.1Gpt
Endonuclease-mediated Allele Detail
Summary
Symbol: S100a16em1.1Gpt
Name: S100 calcium binding protein A16; endonuclease-mediated mutation 1.1, GemPharmatech Co., Ltd
MGI ID: MGI:7398436
Gene: S100a16  Location: Chr3:90444561-90450458 bp, + strand  Genetic Position: Chr3, 39.25 cM, cytoband F1-F2
Alliance: S100a16em1.1Gpt page
Mutation
origin
Strain of Origin:  C57BL/6JGpt
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutations:    Insertion, Intragenic deletion
    CRISPR-targeting floxed exons 2 and 3. Cre-mediated recombination removed exons 2 and 3. (J:330793)
Inheritance:    Not Specified
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 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 S100a16 Mutation:  15 strains or lines available
References
Original:  J:330793 Zhang WS, et al., S100a16 deficiency prevents hepatic stellate cells activation and liver fibrosis via inhibiting CXCR4 expression. Metabolism. 2022 Jul 29;135:155271
All:  3 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
11/19/2024
MGI 6.24
The Jackson Laboratory