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Fcgr3tm1Jsv
Targeted Allele Detail
Summary
Symbol: Fcgr3tm1Jsv
Name: Fc receptor, IgG, low affinity III; targeted mutation 1, J Sjef Verbeek
MGI ID: MGI:1861924
Synonyms: FcgammaRIII-, Fcgr3tm1Sjv
Gene: Fcgr3  Location: Chr1:170878743-170892504 bp, - strand  Genetic Position: Chr1, 78.8 cM
Alliance: Fcgr3tm1Jsv page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:35057
Parent Cell Line:  E14 (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsA hygromycin selection cassette replaced a genomic fragment containing sequences encoding the ligand binding and part of the transmembrane domains. RT-PCR analysis on NK fractions of splenocytes derived from homozygous mice demonstrated that no detectable transcript was produced from this allele. Flow cytometry analysis on NK cells, B lymphocytes, macrophages and neutrophils confirmed that no detectable cell surface protein was encoded by this allele. (J:35057)
Phenotypes
Key:
hm homozygous ht heterozygous tg involves transgenes phenotype observed
cn conditional genotype  cx complex: > 1 genome feature ot other: hemizygous, indeterminate,... N normal phenotype
Genotype/
Background:
Phenotypes:
Affected Systems
show or hide all annotated terms
         
cellular
decreased mast cell degranulation
impaired macrophage phagocytosis
growth/size/body
enlarged spleen
increased spleen weight
hematopoietic system
enlarged spleen
increased spleen weight
decreased susceptibility to autoimmune hemolytic anemia
abnormal leukocyte cell number
increased neutrophil cell number
increased B cell number
increased activated T cell number
abnormal mast cell physiology
decreased mast cell degranulation
abnormal neutrophil physiology
impaired neutrophil recruitment
impaired natural killer cell mediated cytotoxicity
abnormal macrophage physiology
impaired macrophage phagocytosis
immune system
enlarged spleen
increased spleen weight
decreased susceptibility to autoimmune hemolytic anemia
abnormal leukocyte cell number
increased neutrophil cell number
increased B cell number
increased activated T cell number
abnormal mast cell physiology
decreased mast cell degranulation
abnormal neutrophil physiology
impaired neutrophil recruitment
impaired natural killer cell mediated cytotoxicity
abnormal macrophage physiology
impaired macrophage phagocytosis
abnormal dendritic cell antigen presentation
abnormal type I hypersensitivity reaction
increased susceptibility to type I hypersensitivity reaction
decreased susceptibility to type II hypersensitivity reaction
decreased susceptibility to experimental autoimmune encephalomyelitis
decreased susceptibility to induced arthritis
increased anti-chromatin antibody level
increased anti-double stranded DNA antibody level
increased anti-histone antibody level
increased anti-single stranded DNA antibody level
mortality/aging
N
mortality/aging
N
skeleton
decreased susceptibility to induced arthritis
View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 5 strains available      Cell Lines: 0 lines available
Carrying any Fcgr3 Mutation:  29 strains or lines available
References
Original:  J:35057 Hazenbos WL, et al., Impaired IgG-dependent anaphylaxis and Arthus reaction in Fc gamma RIII (CD16) deficient mice. Immunity. 1996 Aug;5(2):181-8
All:  124 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
12/17/2024
MGI 6.24
The Jackson Laboratory

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