abnormal splenocyte morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of a cell of the spleen (Mammalian Phenotype Ontology, MP_0009332)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009332
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Genes

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

Symbol Name
AKAP13 A kinase (PRKA) anchor protein 13
APC adenomatous polyposis coli
ATM ATM serine/threonine kinase
BCL2L11 BCL2-like 11 (apoptosis facilitator)
BLNK B-cell linker
BMF Bcl2 modifying factor
BTK Bruton agammaglobulinemia tyrosine kinase
CD34 CD34 molecule
CRH corticotropin releasing hormone
DCLRE1C DNA cross-link repair 1C
DIDO1 death inducer-obliterator 1
ESRRA estrogen-related receptor alpha
FAS Fas cell surface death receptor
FLT3 fms-related tyrosine kinase 3
FOS FBJ murine osteosarcoma viral oncogene homolog
GATA1 GATA binding protein 1 (globin transcription factor 1)
IKZF1 IKAROS family zinc finger 1 (Ikaros)
IL2 interleukin 2
IRF1 interferon regulatory factor 1
KLF13 Kruppel-like factor 13
LCN2 lipocalin 2
LEP leptin
LEPR leptin receptor
LIG4 ligase IV, DNA, ATP-dependent
MTOR mechanistic target of rapamycin (serine/threonine kinase)
PATZ1 POZ (BTB) and AT hook containing zinc finger 1
PKN1 protein kinase N1
PTPN2 protein tyrosine phosphatase, non-receptor type 2
RFTN1 raftlin, lipid raft linker 1
RNF8 ring finger protein 8, E3 ubiquitin protein ligase
STAT5A signal transducer and activator of transcription 5A
STAT5B signal transducer and activator of transcription 5B
TET2 tet methylcytosine dioxygenase 2
THEMIS thymocyte selection associated
TPX2 TPX2, microtubule-associated
TWSG1 twisted gastrulation BMP signaling modulator 1
USP21 ubiquitin specific peptidase 21
WAS Wiskott-Aldrich syndrome
ZEB1 zinc finger E-box binding homeobox 1
ZFP36L2 ZFP36 ring finger protein-like 2