Phenotype: abnormal spleen white pulp morphology

Definition
any structural anomaly of the parenchymatous tissue of the spleen that surrounds splenic blood vessels, consists of compact masses of lymphatic cells and is where foreign material removed from the blood is used to initiate an immune reaction that results in the production of antibodies
Synonyms
abnormal splenic white pulp morphology
0%
of tested genes
0
significant genes
0
tested genes

IMPC Gene variants with abnormal spleen white pulp morphology

Total number of significant genotype-phenotype associations: 7

Gene / Allele Zygosity Sex Life Stage Phenotype Parameter Phenotyping
Center
P Value
Arhgef1
Arhgef1tm1a(EUCOMM)Wtsi
HOM   Early adult decreased marginal zone B cell number Marginal zone B cells - % of CD45+
Spleen Immunophenotyping
WTSI
3i
0.00
Cog6
Cog6tm1a(EUCOMM)Wtsi
HOM   Early adult decreased marginal zone B cell number Marginal zone B cells - % of B2 cells
Spleen Immunophenotyping
WTSI
3i
0.00
Dph6
Dph6tm1a(KOMP)Wtsi
HOM   Early adult increased marginal zone B cell number Marginal zone B cells - % of CD45+
Spleen Immunophenotyping
WTSI
3i
0.00
Gm5544
Gm5544tm1a(KOMP)Wtsi
HET   Early adult decreased marginal zone B cell number Marginal zone B cells - % of B2 cells
Spleen Immunophenotyping
WTSI
3i
0.00
Bach2
Bach2tm1b(EUCOMM)Wtsi
HOM Early adult decreased marginal zone B cell number MZB (CD21/35 high)
Immunophenotyping
HMGU
IMPC
9.79×10-08
Myoz1
Myoz1tm1b(EUCOMM)Hmgu
HOM   Late adult increased marginal zone B cell number MZB (CD21/35 high)
Immunophenotyping
HMGU
IMPC
8.45×10-05

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 The way we measure

 Phenotype associations stats

1.46% of tested genes with null mutations on a B6N genetic background have a phenotype association to abnormal spleen white pulp morphology (6/411)

2.50% females (1/40) 2.63% males (1/38)

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