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Hnrnpuem1Frk
Endonuclease-mediated Allele Detail
Summary
Symbol: Hnrnpuem1Frk
Name: heterogeneous nuclear ribonucleoprotein U; endonuclease-mediated mutation 1, Wayne N Frankel
MGI ID: MGI:7550686
Synonyms: Hnrnpu113DEL
Gene: Hnrnpu  Location: Chr1:178148673-178165362 bp, - strand  Genetic Position: Chr1, 83.16 cM
Alliance: Hnrnpuem1Frk page
Mutation
origin
Strain of Origin:  C57BL/6NJ
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsCRISPR/Cas9 technology generated an out-of-frame 113-bp deletion in exon 1, resulting in a premature stop codon in exon 2. (J:342579)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Mice Carrying this Mutation: 1 RNA-Seq or microarray experiment(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 Hnrnpu Mutation:  43 strains or lines available
References
Original:  J:342579 Dugger SA, et al., Neurodevelopmental deficits and cell-type-specific transcriptomic perturbations in a mouse model of HNRNPU haploinsufficiency. PLoS Genet. 2023 Oct;19(10):e1010952
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
04/16/2024
MGI 6.23
The Jackson Laboratory