abnormality of pelvic girdle bone morphology Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the bony pelvic girdle, which is a ring of bones connecting the vertebral column to the femurs. (Human Phenotype Ontology, HP_0002644)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0002644
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24 genes associated with the abnormality of pelvic girdle bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
ADGRV1 adhesion G protein-coupled receptor V1 1.22995
NRG1 neuregulin 1 1.12851
NR5A2 nuclear receptor subfamily 5, group A, member 2 1.11517
DLG2 discs, large homolog 2 (Drosophila) 1.0674
CTNNBL1 catenin, beta like 1 1.03592
LMX1A LIM homeobox transcription factor 1, alpha 1.03114
LOC100507377 uncharacterized LOC100507377 1.02289
PLCL1 phospholipase C-like 1 1.00059
CD2AP CD2-associated protein 0.989013
PHACTR1 phosphatase and actin regulator 1 0.978223
CNTNAP2 contactin associated protein-like 2 0.977291
RBMS3 RNA binding motif, single stranded interacting protein 3 0.973975
KCNH8 potassium channel, voltage gated eag related subfamily H, member 8 0.94904
FGF14 fibroblast growth factor 14 0.934145
FMN2 formin 2 0.869608
SAXO1 stabilizer of axonemal microtubules 1 0.867162
FREM1 FRAS1 related extracellular matrix 1 0.85702
PPP6C protein phosphatase 6, catalytic subunit 0.839148
PARD3 par-3 family cell polarity regulator 0.839148
PRR16 proline rich 16 0.819829
PHF20L1 PHD finger protein 20-like 1 0.81297
ZCCHC6 zinc finger, CCHC domain containing 6 0.808534
ARMS2 age-related maculopathy susceptibility 2 0.784165
MTMR2 myotubularin related protein 2 0.614969