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Ighg1em2(IGHG1)Mvw
Endonuclease-mediated Allele Detail
Summary
Symbol: Ighg1em2(IGHG1)Mvw
Name: immunoglobulin heavy constant gamma 1 (G1m marker); endonuclease-mediated mutation 1, Michael V Wiles
MGI ID: MGI:6467517
Synonyms: hFC
Gene: Ighg1  Location: Chr12:113290161-113294143 bp, - strand  Genetic Position: Chr12, 62.1 cM
Alliance: Ighg1em2(IGHG1)Mvw page
Mutation
origin
Mutation
description
Allele Type:    Endonuclease-mediated (Humanized sequence, Inserted expressed sequence)
Mutations:    Insertion, Intragenic deletion
 
Ighg1em2(IGHG1)Mvw expresses 1 gene
 
Mutation detailsCRISPR/cas9 endonuclease-mediated genome editing is used to replace the mouse Ighg1 locus hinge (exon 2), CH2 (exon 3) and CH3 (exon 4) regions with a 902 bp human hinge (exon 2), CH2 (exon 3) and CH3 (exon 4) sequences while preserving the splice junctions. (J:296090)
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 Ighg1 Mutation:  28 strains or lines available
References
Original:  J:296090 Low BE, et al., Functional humanization of immunoglobulin heavy constant gamma 1 Fc domain human FCGRT transgenic mice. MAbs. 2020 Jan-Dec;12(1):1829334
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
06/12/2024
MGI 6.13
The Jackson Laboratory