heterochromia iridis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Heterochromia iridis is a difference in the color of the iris in the two eyes. (Human Phenotype Ontology, HP_0001100)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001100
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Genes

16 genes associated with the heterochromia iridis 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
AKT1 v-akt murine thymoma viral oncogene homolog 1
CHN1 chimerin 1
EDN3 endothelin 3
EDNRB endothelin receptor type B
FGF3 fibroblast growth factor 3
GNAQ guanine nucleotide binding protein (G protein), q polypeptide
IKBKAP inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
LMX1B LIM homeobox transcription factor 1, beta
MITF microphthalmia-associated transcription factor
PAX3 paired box 3
PTEN phosphatase and tensin homolog
SNAI2 snail family zinc finger 2
SOX10 SRY (sex determining region Y)-box 10