small nasal bone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced size of either of two rectangular bone plates forming the bridge of the nose (Mammalian Phenotype Ontology, MP_0004470)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004470
Similar Terms
Downloads & Tools

Genes

34 gene mutations causing the small nasal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALKBH1 alkB, alkylation repair homolog 1 (E. coli)
ANKRD11 ankyrin repeat domain 11
ARID5B AT rich interactive domain 5B (MRF1-like)
BAZ1B bromodomain adjacent to zinc finger domain, 1B
BMP4 bone morphogenetic protein 4
BMP5 bone morphogenetic protein 5
BRD4 bromodomain containing 4
CHST11 carbohydrate (chondroitin 4) sulfotransferase 11
COL2A1 collagen, type II, alpha 1
CREBBP CREB binding protein
DLX5 distal-less homeobox 5
DNMT3B DNA (cytosine-5-)-methyltransferase 3 beta
FGF9 fibroblast growth factor 9
FGFR3 fibroblast growth factor receptor 3
GJA1 gap junction protein, alpha 1, 43kDa
GUSB glucuronidase, beta
HSPG2 heparan sulfate proteoglycan 2
MIR140 microRNA 140
MSX1 msh homeobox 1
NKD1 naked cuticle homolog 1 (Drosophila)
NPR2 natriuretic peptide receptor 2
PHEX phosphate regulating endopeptidase homolog, X-linked
PRDM16 PR domain containing 16
PRKRA protein kinase, interferon-inducible double stranded RNA dependent activator
PSIP1 PC4 and SFRS1 interacting protein 1
RAI1 retinoic acid induced 1
ROR2 receptor tyrosine kinase-like orphan receptor 2
RUNX2 runt-related transcription factor 2
RYK receptor-like tyrosine kinase
SCHIP1 schwannomin interacting protein 1
SH3PXD2B SH3 and PX domains 2B
TCOF1 Treacher Collins-Franceschetti syndrome 1
TGIF1 TGFB-induced factor homeobox 1
TIPARP TCDD-inducible poly(ADP-ribose) polymerase