abnormal secondary palate development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the formation of the part of the palate that is formed during embryonic development when palatal projections from the inner part of the maxillary processes emerge, extend and elevate into a horizontal position above the tongue (Mammalian Phenotype Ontology, MP_0009655)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009655
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Genes

87 gene mutations causing the abnormal secondary palate development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AP2B1 adaptor-related protein complex 2, beta 1 subunit
APAF1 apoptotic peptidase activating factor 1
BMP7 bone morphogenetic protein 7
BNC2 basonuclin 2
CASK calcium/calmodulin-dependent serine protein kinase (MAGUK family)
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CHD7 chromodomain helicase DNA binding protein 7
CHRD chordin
CHUK conserved helix-loop-helix ubiquitous kinase
COL2A1 collagen, type II, alpha 1
CRK v-crk avian sarcoma virus CT10 oncogene homolog
CTGF connective tissue growth factor
DHCR7 7-dehydrocholesterol reductase
DHRS3 dehydrogenase/reductase (SDR family) member 3
DLG1 discs, large homolog 1 (Drosophila)
DLX2 distal-less homeobox 2
EDNRB endothelin receptor type B
EFNB1 ephrin-B1
FGF10 fibroblast growth factor 10
FGF18 fibroblast growth factor 18
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
FLNA filamin A, alpha
FOXE1 forkhead box E1
FOXF2 forkhead box F2
FRAS1 Fraser extracellular matrix complex subunit 1
FUZ fuzzy planar cell polarity protein
GAB1 GRB2-associated binding protein 1
GAD1 glutamate decarboxylase 1 (brain, 67kDa)
GLI2 GLI family zinc finger 2
GRB2 growth factor receptor-bound protein 2
GSK3B glycogen synthase kinase 3 beta
HAND2 heart and neural crest derivatives expressed 2
HHAT hedgehog acyltransferase
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
IRF6 interferon regulatory factor 6
ITGAV integrin, alpha V
ITGB8 integrin, beta 8
JAG2 jagged 2
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2
KDF1 keratinocyte differentiation factor 1
LHX8 LIM homeobox 8
LUZP1 leucine zipper protein 1
MN1 meningioma (disrupted in balanced translocation) 1
MNT MAX network transcriptional repressor
MSX1 msh homeobox 1
NCOA6 nuclear receptor coactivator 6
OSR2 odd-skipped related transciption factor 2
PAK1IP1 PAK1 interacting protein 1
PAX9 paired box 9
PBX1 pre-B-cell leukemia homeobox 1
PDGFC platelet derived growth factor C
PDGFRA platelet-derived growth factor receptor, alpha polypeptide
PDS5A PDS5 cohesin associated factor A
PDS5B PDS5 cohesin associated factor B
PHC1 polyhomeotic homolog 1 (Drosophila)
PITX1 paired-like homeodomain 1
PKDCC protein kinase domain containing, cytoplasmic
PRDM16 PR domain containing 16
PRRX1 paired related homeobox 1
PTCH1 patched 1
RFNG RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
ROR2 receptor tyrosine kinase-like orphan receptor 2
RSPO2 R-spondin 2
RUNX2 runt-related transcription factor 2
SATB2 SATB homeobox 2
SCHIP1 schwannomin interacting protein 1
SFN stratifin
SGPL1 sphingosine-1-phosphate lyase 1
SHOX2 short stature homeobox 2
SIM2 single-minded family bHLH transcription factor 2
SLC32A1 solute carrier family 32 (GABA vesicular transporter), member 1
SNAI2 snail family zinc finger 2
SOX11 SRY (sex determining region Y)-box 11
SOX5 SRY (sex determining region Y)-box 5
TBX1 T-box 1
TBX10 T-box 10
TBX2 T-box 2
TBX3 T-box 3
TCOF1 Treacher Collins-Franceschetti syndrome 1
TGFB2 transforming growth factor, beta 2
TGFB3 transforming growth factor, beta 3
TMEM107 transmembrane protein 107
TP63 tumor protein p63
TSHZ1 teashirt zinc finger homeobox 1
WDR19 WD repeat domain 19
ZEB1 zinc finger E-box binding homeobox 1