absent spleen Gene Set
Genes
17 gene mutations causing the absent spleen phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
CCDC39
|
coiled-coil domain containing 39
|
|
CFC1
|
cripto, FRL-1, cryptic family 1
|
|
DNAH5
|
dynein, axonemal, heavy chain 5
|
|
DRC1
|
dynein regulatory complex subunit 1
|
|
IFT140
|
intraflagellar transport 140
|
|
KAT6A
|
K(lysine) acetyltransferase 6A
|
|
MEGF8
|
multiple EGF-like-domains 8
|
|
MKS1
|
Meckel syndrome, type 1
|
|
NKX2-3
|
NK2 homeobox 3
|
|
NKX3-2
|
NK3 homeobox 2
|
|
PBX1
|
pre-B-cell leukemia homeobox 1
|
|
PCGF3
|
polycomb group ring finger 3
|
|
PKD2
|
polycystic kidney disease 2 (autosomal dominant)
|
|
SOX11
|
SRY (sex determining region Y)-box 11
|
|
TCF21
|
transcription factor 21
|
|
TLX1
|
T-cell leukemia homeobox 1
|
|
WT1
|
Wilms tumor 1
|
