Parietal Foramina Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description NT MGI. (Human Disease Ontology, DOID_0060285)
External Link https://www.disgenet.org/browser/0/1/0/C1865044
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Genes

20 genes associated with the disease Parietal Foramina in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALX1 ALX homeobox 1
ALX3 ALX homeobox 3
ALX4 ALX homeobox 4
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit
CAT catalase
CREBBP CREB binding protein
EP300 E1A binding protein p300
EXT2 exostosin glycosyltransferase 2
FGFR2 fibroblast growth factor receptor 2
IL6 interleukin 6
MSX2 msh homeobox 2
PHF21A PHD finger protein 21A
PRDM5 PR domain containing 5
QTRT1 queuine tRNA-ribosyltransferase 1
RPS19 ribosomal protein S19
SCN4A sodium channel, voltage gated, type IV alpha subunit
TNF tumor necrosis factor
TWIST1 twist family bHLH transcription factor 1
UGT8 UDP glycosyltransferase 8
USP14 ubiquitin specific peptidase 14 (tRNA-guanine transglycosylase)