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Inhbaem2Iimcb
Endonuclease-mediated Allele Detail
Summary
Symbol: Inhbaem2Iimcb
Name: inhibin beta-A; endonuclease-mediated mutation 2, International Institute of Molecular and Cellular Biology in Warsaw
MGI ID: MGI:8214990
Gene: Inhba  Location: Chr13:16186436-16206206 bp, + strand  Genetic Position: Chr13, 5.85 cM
Alliance: Inhbaem2Iimcb page
Mutation
origin
Strain of Origin:  (C57BL/6JTar x CBA/WTar)F1
Mutation
description
Allele Type:    Endonuclease-mediated (Hypomorph)
Mutation:    Insertion
 
Mutation detailsThe mutation involved the insertion of the left LoxP flank into the exon of 5 untranslated region of the first exon of the Inhba gene. The right LoxP sequence is located in the intron downstream of the Inhba gene, along with the XhoI sequence facilitating genotyping. The correct integration of LoxP sites was confirmed in the founder mouse by Sanger sequencing and routinely verified through mice genotyping. (J:368243)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
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: 0 strains available      Cell Lines: 0 lines available
Carrying any Inhba Mutation:  29 strains or lines available
References
Original:  J:368243 Winek E, Direct Data Submissions from the International Institute of Molecular and Cellular Biology in Warsaw. 2025;
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
03/25/2025
MGI 6.24
The Jackson Laboratory