intracranial arterial disease Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

15 genes associated with the disease intracranial arterial disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
SYK spleen tyrosine kinase 0.738873
RNF213 ring finger protein 213 0.486425
RBBP8 retinoblastoma binding protein 8 0.009994
RP1 retinitis pigmentosa 1 (autosomal dominant) 0.009994
SOX17 SRY (sex determining region Y)-box 17 0.009293
CNNM2 cyclin and CBS domain divalent metal cation transport mediator 2 0.008963
STARD13 StAR-related lipid transfer (START) domain containing 13 0.008791
EDNRA endothelin receptor type A 0.008572
BOLL boule-like RNA-binding protein 0.008265
SF3B1 splicing factor 3b, subunit 1, 155kDa 0.008013
ANKRD44 ankyrin repeat domain 44 0.007789
PLCL1 phospholipase C-like 1 0.007651
BET1L Bet1 golgi vesicular membrane trafficking protein-like 0.006542
ALDH2 aldehyde dehydrogenase 2 family (mitochondrial) 0.006542
GPR137B G protein-coupled receptor 137B 0.005701