abnormality of lower limb joint Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0100491
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Genes

15 genes associated with the abnormality of lower limb joint phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
BTNL2 butyrophilin-like 2 0.615522
CDKN2B-AS1 CDKN2B antisense RNA 1 0.578511
ANK1 ankyrin 1, erythrocytic 0.441652
FSTL5 follistatin-like 5 0.437499
UBR2 ubiquitin protein ligase E3 component n-recognin 2 0.415414
CDKN2B cyclin-dependent kinase inhibitor 2B (p15, inhibits CDK4) 0.408541
AHCTF1 AT hook containing transcription factor 1 0.407192
GRIK2 glutamate receptor, ionotropic, kainate 2 0.407145
LINC00578 long intergenic non-protein coding RNA 578 0.406749
LGI1 leucine-rich, glioma inactivated 1 0.40528
PARD3B par-3 family cell polarity regulator beta 0.405267
CCDC38 coiled-coil domain containing 38 0.402228
IDE insulin-degrading enzyme 0.396022
DAB2IP DAB2 interacting protein 0.389484
GRAMD1C GRAM domain containing 1C 0.382146