abnormal splenocyte apoptosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description deviation in the number of spleen cells undergoing programmed cell death (Mammalian Phenotype Ontology, MP_0009340)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009340
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Genes

17 gene mutations causing the abnormal splenocyte apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BCL2 B-cell CLL/lymphoma 2
BRAF B-Raf proto-oncogene, serine/threonine kinase
CASP9 caspase 9, apoptosis-related cysteine peptidase
EEF1E1 eukaryotic translation elongation factor 1 epsilon 1
ETS1 v-ets avian erythroblastosis virus E26 oncogene homolog 1
KLF13 Kruppel-like factor 13
MTOR mechanistic target of rapamycin (serine/threonine kinase)
NCOA3 nuclear receptor coactivator 3
NFE2L2 nuclear factor, erythroid 2-like 2
NFKB2 nuclear factor of kappa light polypeptide gene enhancer in B-cells 2 (p49/p100)
POLB polymerase (DNA directed), beta
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
STEAP3 STEAP family member 3, metalloreductase
TLX1 T-cell leukemia homeobox 1
TP53 tumor protein p53
USP4 ubiquitin specific peptidase 4 (proto-oncogene)
WT1 Wilms tumor 1