vascular skin abnormality 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:0011276
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Genes

23 genes associated with the vascular skin abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
CRACR2A calcium release activated channel regulator 2A 1.04365
NREP neuronal regeneration related protein 1.01962
ALDH1A1 aldehyde dehydrogenase 1 family, member A1 0.986868
LMO1 LIM domain only 1 (rhombotin 1) 0.918733
TMEM100 transmembrane protein 100 0.764625
CPNE4 copine IV 0.757258
ETV6 ets variant 6 0.737679
PRKCQ protein kinase C, theta 0.7273
ACCSL 1-aminocyclopropane-1-carboxylate synthase homolog (Arabidopsis)(non-functional)-like 0.69768
ORC5 origin recognition complex, subunit 5 0.691208
IVD isovaleryl-CoA dehydrogenase 0.690274
SEMA5B sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B 0.685142
DACH1 dachshund family transcription factor 1 0.651454
BEND6 BEN domain containing 6 0.650754
RELN reelin 0.640092
GALNT18 polypeptide N-acetylgalactosaminyltransferase 18 0.638927
OPCML opioid binding protein/cell adhesion molecule-like 0.624663
PLXNC1 plexin C1 0.624461
RAD52 RAD52 homolog (S. cerevisiae) 0.599941
GTF2A1 general transcription factor IIA, 1, 19/37kDa 0.596866
MPDZ multiple PDZ domain protein 0.594193
GRXCR1 glutaredoxin, cysteine rich 1 0.589497
MTHFD1L methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1-like 0.586009