absent spleen Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000690
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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