Phenotype: abnormal B-1 B cell morphology

Definition
any structural anomaly of the subset of B cells found predominantly in the peritoneum, pleural cavities, and spleen, and are enriched for self-reactivity; B-1 B cells are thought to be the primary source of natural IgM immunoglobulin, that is, IgM produced in large quantities without prior antigenic stimulation and generally reactive against various microorganisms, as well as the source of T-independent IgA immunoglobulin in the mucosal areas
Synonyms
abnormal B-1 B-lymphocyte morphology,  abnormal B-1 B lymphocyte morphology,  abnormal B-1 B-cell morphology,  abnormal B1 cell morphology
0%
of tested genes
0
significant genes
0
tested genes

IMPC Gene variants with abnormal B-1 B cell morphology

Total number of significant genotype-phenotype associations: 2

Gene / Allele Zygosity Sex Life Stage Phenotype Parameter Phenotyping
Center
P Value
Arhgap17
Arhgap17tm1b(EUCOMM)Wtsi
HOM   Early adult decreased B-1a cell number B1a cells - % of CD45+
Spleen Immunophenotyping
WTSI
3i
0.00
Bach2
Bach2tm1b(EUCOMM)Wtsi
HOM Early adult decreased B-1a cell number B1B Cells
Immunophenotyping
HMGU
IMPC
3.10×10-05

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 The way we measure

 Phenotype associations stats

2.38% of tested genes with null mutations on a B6N genetic background have a phenotype association to abnormal B-1 B cell morphology (2/84)

1.32% females (1/76) 0.00% males (0/73)

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