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TfrcRbc6
Chemically induced Allele Detail
Summary
Symbol: TfrcRbc6
Name: transferrin receptor; red blood cell mutant 6
MGI ID: MGI:6406247
Synonyms: tfrcL645R
Gene: Tfrc  Location: Chr16:32427738-32451612 bp, + strand  Genetic Position: Chr16, 23.06 cM
Alliance: TfrcRbc6 page
Mutation
origin
Strain of Origin:  C57BL/6
Mutation
description
Allele Type:    Chemically induced (ENU) (Not Specified)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced a T to G point mutation that results in the amino acid substitution of arginine for leucine at position 645 (L645R). (J:285514)
Inheritance:    Dominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 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 Tfrc Mutation:  64 strains or lines available
References
Original:  J:285514 Conway AJ, et al., Characterization of Tfrc-mutant mice with microcytic phenotypes. Blood Adv. 2018 Aug 14;2(15):1914-1922
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
10/29/2024
MGI 6.24
The Jackson Laboratory