short nasal bone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced length of either of two rectangular bone plates forming the bridge of the nose (Mammalian Phenotype Ontology, MP_0004471)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004471
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Genes

27 gene mutations causing the short 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
DLX5 distal-less homeobox 5
DNMT3B DNA (cytosine-5-)-methyltransferase 3 beta
FGF9 fibroblast growth factor 9
FGFR3 fibroblast growth factor receptor 3
HSPG2 heparan sulfate proteoglycan 2
MIR140 microRNA 140
NKD1 naked cuticle homolog 1 (Drosophila)
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
RYK receptor-like tyrosine kinase
SCHIP1 schwannomin interacting protein 1
SH3PXD2B SH3 and PX domains 2B
TGIF1 TGFB-induced factor homeobox 1
TIPARP TCDD-inducible poly(ADP-ribose) polymerase