abnormality of the diencephalon Gene Set
Genes
17 genes associated with the abnormality of the diencephalon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ANOS1
|
anosmin 1
|
|
BAZ1B
|
bromodomain adjacent to zinc finger domain, 1B
|
|
CLIP2
|
CAP-GLY domain containing linker protein 2
|
|
ELN
|
elastin
|
|
GLI3
|
GLI family zinc finger 3
|
|
GTF2I
|
general transcription factor IIi
|
|
GTF2IRD1
|
GTF2I repeat domain containing 1
|
|
LEPR
|
leptin receptor
|
|
LIMK1
|
LIM domain kinase 1
|
|
NDP
|
Norrie disease (pseudoglioma)
|
|
OFD1
|
oral-facial-digital syndrome 1
|
|
PTCH1
|
patched 1
|
|
RFC2
|
replication factor C (activator 1) 2, 40kDa
|
|
SCP2
|
sterol carrier protein 2
|
|
SOX2
|
SRY (sex determining region Y)-box 2
|
|
TBL2
|
transducin (beta)-like 2
|
|
TRH
|
thyrotropin-releasing hormone
|
