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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Clec4dtm1.1Shoy
targeted mutation 1.1, Sho Yamasaki
MGI:5528858
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Clec4dtm1.1Shoy/Clec4dtm1.1Shoy involves: 129P2/OlaHsd * C57BL/6 MGI:5528880


Genotype
MGI:5528880
hm1
Allelic
Composition
Clec4dtm1.1Shoy/Clec4dtm1.1Shoy
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Clec4dtm1.1Shoy mutation (0 available); any Clec4d mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• in mice treated with oil-in-water emulsion of trehalose-6,60'-dimycolate (TDM)

immune system
• mice exhibit impaired TDM-induced thymic atrophy compared with wild-type mice
• TDM-treated mice exhibit less of an increase in draining lymph nodes dendritic cells compared with wild-type mice
• TDM-treated mice immunized with ovalbumin exhibit reduced footpad swelling and anti-ovalbumin IgG compared with wild-type mice
• impaired antigen presenting cell function
• in TDM-treated mice immunized with ovalbumin
• in mice re-challenged with MOG antigen and pertussis toxin 20 days after immunization for EAE
• bone marrow-derived dendritic cells and macrophages stimulated with platelets coated in trehalose-6,60'-dimycolate (TDM) or zymosan exhibit reduced MIP-2 secretion compared with wild-type cells
• TDM-treated bone marrow dendritic cells co-cultured with OT-II cells and OVA323-339 or OVA257-264 peptide or ovalbumin protein exhibit less of an increase in IFN-gamma and IL17 compared with wild-type cells
• TDM-treated bone marrow dendritic cells co-cultured with OT-II cells and OVA323-339 peptide exhibit less of an increase in IFN-gamma and IL17 compared with wild-type cells
• in bone marrow-derived dendritic cells and macrophages stimulated with platelets coated in TDM or zymosan
• almost completely abrogated with reduced skin inflammation in TDM-treated mice
• in mice treated with TDM but not as severe as in wild-type mice
• in mice treated with TDM but not as severe as in wild-type mice
• mice infected with Mycobacterium bovis BCG exhibit reduced IFN-gamma production in response to PPD compared with wild-type mice

respiratory system
• in mice treated with TDM but not as severe as in wild-type mice

homeostasis/metabolism
• in mice re-challenged with MOG antigen and pertussis toxin 20 days after immunization for EAE
• in mice treated with oil-in-water emulsion of trehalose-6,60'-dimycolate (TDM)
• mice treated with TDM exhibit reduced lung inflammation, granuloma area and lethality compared with wild-type mice

hematopoietic system
• mice exhibit impaired TDM-induced thymic atrophy compared with wild-type mice
• TDM-treated mice exhibit less of an increase in draining lymph nodes dendritic cells compared with wild-type mice
• in TDM-treated mice immunized with ovalbumin

endocrine/exocrine glands
• mice exhibit impaired TDM-induced thymic atrophy compared with wild-type mice





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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
05/07/2024
MGI 6.23
The Jackson Laboratory