Spondylometaphyseal Dysplasia Gene Set
Genes
16 genes associated with the disease Spondylometaphyseal Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
AGRP
|
agouti related neuropeptide
|
|
ARNTL
|
aryl hydrocarbon receptor nuclear translocator-like
|
|
ARTN
|
artemin
|
|
C21ORF2
|
chromosome 21 open reading frame 2
|
|
COL2A1
|
collagen, type II, alpha 1
|
|
FN1
|
fibronectin 1
|
|
GAL
|
galanin/GMAP prepropeptide
|
|
GPX4
|
glutathione peroxidase 4
|
|
IFT20
|
intraflagellar transport 20
|
|
NEK1
|
NIMA-related kinase 1
|
|
PCYT1A
|
phosphate cytidylyltransferase 1, choline, alpha
|
|
PSD4
|
pleckstrin and Sec7 domain containing 4
|
|
RPS19
|
ribosomal protein S19
|
|
SLC51A
|
solute carrier family 51, alpha subunit
|
|
TRIP11
|
thyroid hormone receptor interactor 11
|
|
TRPV4
|
transient receptor potential cation channel, subfamily V, member 4
|
