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Hkdc1em1Xjz
Endonuclease-mediated Allele Detail
Summary
Symbol: Hkdc1em1Xjz
Name: hexokinase domain containing 1; endonuclease-mediated mutation 1, Xianjun Zhu
MGI ID: MGI:6379689
Synonyms: Mut1
Gene: Hkdc1  Location: Chr10:62218916-62258270 bp, - strand  Genetic Position: Chr10, 32.4 cM
Alliance: Hkdc1em1Xjz page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsCRISPR/Cas9-mediated genome editing technology was used to generate a 7bp deletion in exon 2. The mutation results in a shift in the reading frame, resulting in a truncation of the encoded protein. (J:266978)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Hkdc1 Mutation:  39 strains or lines available
References
Original:  J:266978 Zhang L, et al., Whole-exome sequencing revealed HKDC1 as a candidate gene associated with autosomal-recessive retinitis pigmentosa. Hum Mol Genet. 2018 Dec 1;27(23):4157-4168
All:  2 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
11/12/2024
MGI 6.24
The Jackson Laboratory