trigonocephaly Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Wedge-shaped, or triangular head, with the apex of the triangle at the midline of the forehead and the base of the triangle at the occiput. (Human Phenotype Ontology, HP_0000243)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000243
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Genes

17 genes associated with the trigonocephaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACTB actin, beta
ACTG1 actin gamma 1
ASXL1 additional sex combs like transcriptional regulator 1
C2CD3 C2 calcium-dependent domain containing 3
CD96 CD96 molecule
EFTUD2 elongation factor Tu GTP binding domain containing 2
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
FREM1 FRAS1 related extracellular matrix 1
GLI3 GLI family zinc finger 3
IL11RA interleukin 11 receptor, alpha
MEGF8 multiple EGF-like-domains 8
PDHX pyruvate dehydrogenase complex, component X
PTCH1 patched 1
RB1 retinoblastoma 1
SRCAP Snf2-related CREBBP activator protein
ZIC2 Zic family member 2