absent eyebrow Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence of the eyebrow. (Human Phenotype Ontology, HP_0002223)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002223
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Genes

11 genes associated with the absent eyebrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALX1 ALX homeobox 1
BRAF B-Raf proto-oncogene, serine/threonine kinase
EDA ectodysplasin A
FRAS1 Fraser extracellular matrix complex subunit 1
FREM2 FRAS1 related extracellular matrix protein 2
GRIP1 glutamate receptor interacting protein 1
KRAS Kirsten rat sarcoma viral oncogene homolog
KRT85 keratin 85, type II
MBTPS2 membrane-bound transcription factor peptidase, site 2
RIPK4 receptor-interacting serine-threonine kinase 4
SOX18 SRY (sex determining region Y)-box 18