mandible hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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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
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