mandible hypoplasia Gene Set
Genes
23 gene mutations causing the mandible hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
ACVR2A
|
activin A receptor, type IIA
|
|
ASXL1
|
additional sex combs like transcriptional regulator 1
|
|
CNBP
|
CCHC-type zinc finger, nucleic acid binding protein
|
|
DLG1
|
discs, large homolog 1 (Drosophila)
|
|
ECE1
|
endothelin converting enzyme 1
|
|
EDN1
|
endothelin 1
|
|
EDNRA
|
endothelin receptor type A
|
|
EYA1
|
EYA transcriptional coactivator and phosphatase 1
|
|
FGFRL1
|
fibroblast growth factor receptor-like 1
|
|
FUZ
|
fuzzy planar cell polarity protein
|
|
GPC3
|
glypican 3
|
|
GSC
|
goosecoid homeobox
|
|
HAND2
|
heart and neural crest derivatives expressed 2
|
|
MKS1
|
Meckel syndrome, type 1
|
|
NABP2
|
nucleic acid binding protein 2
|
|
PRDM16
|
PR domain containing 16
|
|
PRRX1
|
paired related homeobox 1
|
|
RPGRIP1L
|
RPGRIP1-like
|
|
SC5D
|
sterol-C5-desaturase
|
|
SMAD2
|
SMAD family member 2
|
|
TCOF1
|
Treacher Collins-Franceschetti syndrome 1
|
|
TMEM67
|
transmembrane protein 67
|
|
ZEB1
|
zinc finger E-box binding homeobox 1
|
