small maxilla Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Underdevelopment of the Maxilla. (Human Phenotype Ontology, HP_0000327)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004540
Similar Terms
Downloads & Tools

Genes

41 gene mutations causing the small maxilla phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALX1 ALX homeobox 1
ARID5B AT rich interactive domain 5B (MRF1-like)
ARSB arylsulfatase B
BCL11B B-cell CLL/lymphoma 11B (zinc finger protein)
BMP5 bone morphogenetic protein 5
CHST11 carbohydrate (chondroitin 4) sulfotransferase 11
CREBBP CREB binding protein
DLX5 distal-less homeobox 5
FGF18 fibroblast growth factor 18
FGFR2 fibroblast growth factor receptor 2
FUZ fuzzy planar cell polarity protein
GJA1 gap junction protein, alpha 1, 43kDa
GLI2 GLI family zinc finger 2
HOXA3 homeobox A3
HRAS Harvey rat sarcoma viral oncogene homolog
LMNA lamin A/C
LTBP1 latent transforming growth factor beta binding protein 1
LTBP3 latent transforming growth factor beta binding protein 3
MIR140 microRNA 140
MMP14 matrix metallopeptidase 14 (membrane-inserted)
MMP2 matrix metallopeptidase 2
MSX1 msh homeobox 1
NPR2 natriuretic peptide receptor 2
PAX7 paired box 7
PHEX phosphate regulating endopeptidase homolog, X-linked
PKDCC protein kinase domain containing, cytoplasmic
PRDM16 PR domain containing 16
SATB2 SATB homeobox 2
SCHIP1 schwannomin interacting protein 1
SH3PXD2B SH3 and PX domains 2B
SIX1 SIX homeobox 1
SLC39A13 solute carrier family 39 (zinc transporter), member 13
SOX11 SRY (sex determining region Y)-box 11
TCOF1 Treacher Collins-Franceschetti syndrome 1
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TIPARP TCDD-inducible poly(ADP-ribose) polymerase
TP63 tumor protein p63
TRPS1 trichorhinophalangeal syndrome I
WDR19 WD repeat domain 19
ZEB1 zinc finger E-box binding homeobox 1
ZIC3 Zic family member 3