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Fth1tm1.2Lck
Targeted Allele Detail
Nomenclature
Symbol: Fth1tm1.2Lck
Name: ferritin heavy polypeptide 1; targeted mutation 1.2, Lukas C Kuhn
MGI ID: MGI:4847967
Gene: Fth1  Location: Chr19:9982703-9985092 bp, + strand  Genetic Position: Chr19, 6.23 cM, cytoband A-C
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:166515
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129/Sv
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
    Cre-mediated recombination removed the promoter and exon 1. (J:166515)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Fth1 Mutation:  5 strains or lines available
References
Original:  J:166515 Darshan D, et al., Conditional deletion of ferritin H in mice induces loss of iron storage and liver damage. Hepatology. 2009 Sep;50(3):852-60
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
05/16/2017
MGI 6.09
The Jackson Laboratory