cranial nerve disease Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description A neuropathy that is located_in one of the twelve cranial nerves. (Human Disease Ontology, DOID_5656)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:5656
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Genes

16 genes associated with the disease cranial nerve disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
ATOH7 atonal homolog 7 (Drosophila) 1.82268
CDKN2B cyclin-dependent kinase inhibitor 2B (p15, inhibits CDK4) 1.80795
DCLK1 doublecortin-like kinase 1 1.42467
CHEK2 checkpoint kinase 2 1.42467
BCAS3 breast carcinoma amplified sequence 3 1.37327
RERE arginine-glutamic acid dipeptide (RE) repeats 1.33878
MYPN myopalladin 1.28906
RFTN1 raftlin, lipid raft linker 1 1.28906
LRP1B low density lipoprotein receptor-related protein 1B 1.26953
ARID3A AT rich interactive domain 3A (BRIGHT-like) 1.26953
SCFD2 sec1 family domain containing 2 1.14463
DENND2A DENN/MADD domain containing 2A 1.07599
TSHR thyroid stimulating hormone receptor 1.07599
ESRRG estrogen-related receptor gamma 1.00407
PEX14 peroxisomal biogenesis factor 14 1.00407
MYH9 myosin, heavy chain 9, non-muscle 0.971169