small frontal bone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced size of the bone forming the forehead and roof of the eye orbit (Mammalian Phenotype Ontology, MP_0004377)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004377
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Genes

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

Symbol Name
ALX1 ALX homeobox 1
BMP1 bone morphogenetic protein 1
BNC2 basonuclin 2
FGFR2 fibroblast growth factor receptor 2
GJA1 gap junction protein, alpha 1, 43kDa
NXN nucleoredoxin
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
SCUBE1 signal peptide, CUB domain, EGF-like 1
TCOF1 Treacher Collins-Franceschetti syndrome 1
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TGFB2 transforming growth factor, beta 2