abnormal b-2 b cell morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of a conventional B cell subject to antigenic stimulation and dependent on T cell help and with a distinct surface marker expression pattern from B-1 B cells (Mammalian Phenotype Ontology, MP_0008166)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008166
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Genes

16 gene mutations causing the abnormal b-2 b cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARID3A AT rich interactive domain 3A (BRIGHT-like)
ATP11C ATPase, class VI, type 11C
BCL2L11 BCL2-like 11 (apoptosis facilitator)
CD72 CD72 molecule
FNIP1 folliculin interacting protein 1
MIR150 microRNA 150
NFKB2 nuclear factor of kappa light polypeptide gene enhancer in B-cells 2 (p49/p100)
NFKBIA nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha
PAX5 paired box 5
PFDN1 prefoldin subunit 1
PIK3CD phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit delta
PLCG2 phospholipase C, gamma 2 (phosphatidylinositol-specific)
PTPRJ protein tyrosine phosphatase, receptor type, J
SPPL2A signal peptide peptidase like 2A
TLR8 toll-like receptor 8
TNFRSF13C tumor necrosis factor receptor superfamily, member 13C