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Sbsponem1Gpt
Endonuclease-mediated Allele Detail
Summary
Symbol: Sbsponem1Gpt
Name: somatomedin B and thrombospondin, type 1 domain containing; endonuclease-mediated mutation 1, GemPharmatech
MGI ID: MGI:8332027
Synonyms: Sbsponem1Cd
Gene: Sbspon  Location: Chr1:15924086-15962946 bp, - strand  Genetic Position: Chr1, 4.89 cM
Alliance: Sbsponem1Gpt page
IMPC: Sbspon gene page
Mutation
origin
Strain of Origin:  C57BL/6JGpt
Project Collection: IMPC
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
    CRISPR/cas9-mediated recombination using two guide RNAs created a 113 bp deletion in exon 2. (J:370648)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 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 Sbspon Mutation:  22 strains or lines available
References
Original:  J:370648 Ni B, et al., Novel glycoprotein SBSPON suppressed bladder cancer through the AKT signal pathway by inhibiting HSPA5 membrane translocation. Int J Biol Sci. 2025;21(10):4586-4603
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
05/12/2026
MGI 6.24
The Jackson Laboratory