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Efhd1em1Wei
Endonuclease-mediated Allele Detail
Summary
Symbol: Efhd1em1Wei
Name: EF hand domain containing 1; endonuclease-mediated mutation 1, Weizmann Institute of Science
MGI ID: MGI:6711681
Gene: Efhd1  Location: Chr1:87192085-87238561 bp, + strand  Genetic Position: Chr1, 44.15 cM
Alliance: Efhd1em1Wei page
Mutation
origin
Strain of Origin:  Not Applicable
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsCRISPR-targeting of the promoter and exon 1 produced a null allele. Western blot analysis confirmed the absence of protein expression in dorsal root ganglia. (J:305107)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 15 assay results
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 Efhd1 Mutation:  20 strains or lines available
References
Original:  J:305107 Ulisse V, et al., Regulation of axonal morphogenesis by the mitochondrial protein Efhd1. Life Sci Alliance. 2020 Jul;3(7)
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
10/29/2024
MGI 6.24
The Jackson Laboratory