abnormal b-1a b cell morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the B-1 B cell subset bearing the CD5 surface marker (Mammalian Phenotype Ontology, MP_0008164)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008164
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Genes

33 gene mutations causing the abnormal b-1a 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
AVPR1A arginine vasopressin receptor 1A
BANK1 B-cell scaffold protein with ankyrin repeats 1
BLNK B-cell linker
BTK Bruton agammaglobulinemia tyrosine kinase
CARD11 caspase recruitment domain family, member 11
CD72 CD72 molecule
CD79A CD79a molecule, immunoglobulin-associated alpha
CD79B CD79b molecule, immunoglobulin-associated beta
CD81 CD81 molecule
CDH17 cadherin 17, LI cadherin (liver-intestine)
CR2 complement component (3d/Epstein Barr virus) receptor 2
DAPP1 dual adaptor of phosphotyrosine and 3-phosphoinositides
ETS1 v-ets avian erythroblastosis virus E26 oncogene homolog 1
HAX1 HCLS1 associated protein X-1
IGHM immunoglobulin heavy constant mu
IKZF1 IKAROS family zinc finger 1 (Ikaros)
IL6ST interleukin 6 signal transducer
MALT1 MALT1 paracaspase
NFKBID nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, delta
PIK3AP1 phosphoinositide-3-kinase adaptor protein 1
PLCL2 phospholipase C-like 2
PRKCB protein kinase C, beta
SAMSN1 SAM domain, SH3 domain and nuclear localization signals 1
SEMA4D sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D
SFN stratifin
SIAE sialic acid acetylesterase
SIGLEC10 sialic acid binding Ig-like lectin 10
SPI1 Spi-1 proto-oncogene
THEMIS thymocyte selection associated
TLR8 toll-like receptor 8
ZEB1 zinc finger E-box binding homeobox 1