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Del(X)91H
Endonuclease-mediated Allele Detail
Summary
Symbol: Del(X)91H
Name: deletion, Chr X, Harwell 91
MGI ID: MGI:8237956
Synonyms: ChrXem1H
Gene: Del(X)91H  Location: unknown  Genetic Position: ChrX, Syntenic
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Endonuclease-mediated (Not Specified)
Mutation:    Intergenic deletion
 
Mutation detailsThis is a point mutation model made using CRISPR/Cas9 mediated deletion of 57,886 bp nucleotides from chromosome X (X:84920291-84978177; GRCm39). (J:361968)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any Del(X)91H Mutation:  1 strain or line available
References
Original:  J:361968 Mary Lyon Centre at MRC Harwell, Direct data submission from Mary Lyon Centre at MRC Harwell. 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
01/28/2026
MGI 6.24
The Jackson Laboratory