spleen atrophy Gene Set
Genes
19 gene mutations causing the spleen atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
ABL1
|
ABL proto-oncogene 1, non-receptor tyrosine kinase
|
|
ASXL1
|
additional sex combs like transcriptional regulator 1
|
|
BCL2
|
B-cell CLL/lymphoma 2
|
|
CD2AP
|
CD2-associated protein
|
|
HTRA2
|
HtrA serine peptidase 2
|
|
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
|
|
NKX2-3
|
NK2 homeobox 3
|
|
PARL
|
presenilin associated, rhomboid-like
|
|
PSIP1
|
PC4 and SFRS1 interacting protein 1
|
|
RORA
|
RAR-related orphan receptor A
|
|
RRM2B
|
ribonucleotide reductase M2 B (TP53 inducible)
|
|
SCG5
|
secretogranin V
|
|
STK36
|
serine/threonine kinase 36
|
|
TCF3
|
transcription factor 3
|
|
TDP2
|
tyrosyl-DNA phosphodiesterase 2
|
|
TERT
|
telomerase reverse transcriptase
|
|
TRAF2
|
TNF receptor-associated factor 2
|
|
WWOX
|
WW domain containing oxidoreductase
|
