abnormal palatal shelf elevation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the process in which the palatal shelves move from a vertical position in the orofacial cavity to a horizontal apposition above the developing tongue (Mammalian Phenotype Ontology, MP_0009885)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009885
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31 gene mutations causing the abnormal palatal shelf elevation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CTGF connective tissue growth factor
DHRS3 dehydrogenase/reductase (SDR family) member 3
DLG1 discs, large homolog 1 (Drosophila)
EDNRB endothelin receptor type B
FGF18 fibroblast growth factor 18
FGFR1 fibroblast growth factor receptor 1
FLNA filamin A, alpha
FOXF2 forkhead box F2
FUZ fuzzy planar cell polarity protein
GAD1 glutamate decarboxylase 1 (brain, 67kDa)
GLI2 GLI family zinc finger 2
GSK3B glycogen synthase kinase 3 beta
HAND2 heart and neural crest derivatives expressed 2
HHAT hedgehog acyltransferase
IRF6 interferon regulatory factor 6
JAG2 jagged 2
MNT MAX network transcriptional repressor
PAX9 paired box 9
PDGFC platelet derived growth factor C
PITX1 paired-like homeodomain 1
PKDCC protein kinase domain containing, cytoplasmic
PRDM16 PR domain containing 16
RFNG RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
ROR2 receptor tyrosine kinase-like orphan receptor 2
RSPO2 R-spondin 2
SLC32A1 solute carrier family 32 (GABA vesicular transporter), member 1
SOX5 SRY (sex determining region Y)-box 5
TBX10 T-box 10
TBX2 T-box 2
TCOF1 Treacher Collins-Franceschetti syndrome 1
TGFB2 transforming growth factor, beta 2