CRISPR/Cas9 technology knocked in the human transferrin receptor apical domain coding sequence into the locus creating a chimeric mouse/human transferring receptor under the control of the endogenous promotor which preserves the native murine transferrin ligand binding domain and retains the majority of Tfrc introns, minimizing potential dysregulation of protein expression and function. (J:325423)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6
Endonuclease-mediated
Insertion
--
1
3
3

Phenotypes

Legend:
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes:
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Phenotypes

References Literature

Title
PMID
Journal
Year
IF
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