short frontal bone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced length of the bone forming the forehead and roof of the eye orbit (Mammalian Phenotype Ontology, MP_0004380)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004380
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Genes

7 gene mutations causing the short frontal 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
BMP4 bone morphogenetic protein 4
CRKL v-crk avian sarcoma virus CT10 oncogene homolog-like
FGFR3 fibroblast growth factor receptor 3
PHEX phosphate regulating endopeptidase homolog, X-linked
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3