abnormal hyoid bone morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the U-shaped bone lying between the mandible and the larynx that supports the tongue muscles (Mammalian Phenotype Ontology, MP_0003056)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003056
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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