amaurosis fugax Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A transient visual disturbance that is typically caused by a circulatory, ocular or neurological underlying condition. (Human Phenotype Ontology, HP_0100576)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100576
Similar Terms
Downloads & Tools

Genes

32 genes associated with the amaurosis fugax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADRA2B adrenoceptor alpha 2B
CALR calreticulin
CECR1 cat eye syndrome chromosome region, candidate 1
CNTN2 contactin 2 (axonal)
COX1
COX2
COX3
HLA-B major histocompatibility complex, class I, B
IL12B interleukin 12B
JAK2 Janus kinase 2
MLH1 mutL homolog 1
MLX MLX, MAX dimerization protein
MPL MPL proto-oncogene, thrombopoietin receptor
MSH2 mutS homolog 2
MSH6 mutS homolog 6
MT-ND4 NADH dehydrogenase, subunit 4 (complex I)
MT-ND5 NADH dehydrogenase, subunit 5 (complex I)
MT-ND6 NADH dehydrogenase, subunit 6 (complex I)
MT-TF tRNA
MT-TH tRNA
MT-TL1 tRNA
MT-TQ tRNA
MT-TS1 tRNA
MT-TS2 tRNA
MT-TW tRNA
ND1
NOTCH3 notch 3
PMS2 PMS2 postmeiotic segregation increased 2 (S. cerevisiae)
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
SH2B3 SH2B adaptor protein 3
TET2 tet methylcytosine dioxygenase 2
TP53 tumor protein p53