short maxilla Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced length of the upper jaw bone (Mammalian Phenotype Ontology, MP_0000097)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000097
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Genes

33 gene mutations causing the short 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
FGFR2 fibroblast growth factor receptor 2
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
SATB2 SATB homeobox 2
SCHIP1 schwannomin interacting protein 1
SH3PXD2B SH3 and PX domains 2B
SIX1 SIX homeobox 1
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
TRPS1 trichorhinophalangeal syndrome I
ZEB1 zinc finger E-box binding homeobox 1