spinal rigidity Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Reduced ability to move the vertebral column with a resulting limitation of neck and trunk flexion. (Human Phenotype Ontology, HP_0003306)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0003306
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21 genes associated with the spinal rigidity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
MICA MHC class I polypeptide-related sequence A 2.95015
ERAP1 endoplasmic reticulum aminopeptidase 1 2.15785
IL23R interleukin 23 receptor 1.84688
TRIM31 tripartite motif containing 31 1.57598
KIF21B kinesin family member 21B 1.52822
CAST calpastatin 1.44221
SLC17A2 solute carrier family 17, member 2 1.22817
ANO6 anoctamin 6 1.21853
ANTXR2 anthrax toxin receptor 2 1.15743
CARD9 caspase recruitment domain family, member 9 1.04365
BTN2A1 butyrophilin, subfamily 2, member A1 1.03217
SLC17A3 solute carrier family 17 (organic anion transporter), member 3 0.969142
MALRD1 MAM and LDL receptor class A domain containing 1 0.942765
CSF2RB colony stimulating factor 2 receptor, beta, low-affinity (granulocyte-macrophage) 0.855449
GRAMD1B GRAM domain containing 1B 0.752335
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A 0.734535
PTPN1 protein tyrosine phosphatase, non-receptor type 1 0.630903
SARM1 sterile alpha and TIR motif containing 1 0.620705
TMEM97 transmembrane protein 97 0.561769
C6ORF183 chromosome 6 open reading frame 183 0.526276
CDH13 cadherin 13 0.525663