abnormal hyoid bone morphology Gene Set
Genes
30 gene mutations causing the abnormal hyoid bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
ASXL1
|
additional sex combs like transcriptional regulator 1
|
|
BMP5
|
bone morphogenetic protein 5
|
|
BMP7
|
bone morphogenetic protein 7
|
|
CHRD
|
chordin
|
|
COL2A1
|
collagen, type II, alpha 1
|
|
DLX5
|
distal-less homeobox 5
|
|
DLX6
|
distal-less homeobox 6
|
|
EDN1
|
endothelin 1
|
|
EDNRA
|
endothelin receptor type A
|
|
EYA1
|
EYA transcriptional coactivator and phosphatase 1
|
|
FGFR1
|
fibroblast growth factor receptor 1
|
|
FGFR3
|
fibroblast growth factor receptor 3
|
|
FGFRL1
|
fibroblast growth factor receptor-like 1
|
|
FOXC1
|
forkhead box C1
|
|
HAND2
|
heart and neural crest derivatives expressed 2
|
|
HOXA2
|
homeobox A2
|
|
HOXA3
|
homeobox A3
|
|
MAFB
|
v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog B
|
|
NKX3-2
|
NK3 homeobox 2
|
|
PBX1
|
pre-B-cell leukemia homeobox 1
|
|
PDS5B
|
PDS5 cohesin associated factor B
|
|
RARA
|
retinoic acid receptor, alpha
|
|
RUNX2
|
runt-related transcription factor 2
|
|
SATB2
|
SATB homeobox 2
|
|
SIX1
|
SIX homeobox 1
|
|
SOX9
|
SRY (sex determining region Y)-box 9
|
|
TBX1
|
T-box 1
|
|
WNT9A
|
wingless-type MMTV integration site family, member 9A
|
|
ZIC3
|
Zic family member 3
|
|
ZNF521
|
zinc finger protein 521
|
