abnormal igg2c level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description deviation from the normal levels of immunoglobulin class G2c level (Mammalian Phenotype Ontology, MP_0020178)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0020178
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Genes

14 gene mutations causing the abnormal igg2c level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BATF basic leucine zipper transcription factor, ATF-like
CARD11 caspase recruitment domain family, member 11
CD274 CD274 molecule
CD36 CD36 molecule (thrombospondin receptor)
CD79A CD79a molecule, immunoglobulin-associated alpha
CR2 complement component (3d/Epstein Barr virus) receptor 2
DLK1 delta-like 1 homolog (Drosophila)
ICOS inducible T-cell co-stimulator
IGHG1 immunoglobulin heavy constant gamma 1 (G1m marker)
IL4 interleukin 4
NLRP6 NLR family, pyrin domain containing 6
PYCARD PYD and CARD domain containing
RGS13 regulator of G-protein signaling 13
TRAF3IP2 TRAF3 interacting protein 2