aplasia/hypoplasia of the vertebrae Gene Set
Genes
13 genes associated with the aplasia/hypoplasia of the vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ACVR1
|
activin A receptor, type I
|
|
COL11A1
|
collagen, type XI, alpha 1
|
|
FLNB
|
filamin B, beta
|
|
GLB1
|
galactosidase, beta 1
|
|
INPPL1
|
inositol polyphosphate phosphatase-like 1
|
|
LBR
|
lamin B receptor
|
|
NSDHL
|
NAD(P) dependent steroid dehydrogenase-like
|
|
PRKAR1A
|
protein kinase, cAMP-dependent, regulatory, type I, alpha
|
|
RPS19
|
ribosomal protein S19
|
|
SLC26A2
|
solute carrier family 26 (anion exchanger), member 2
|
|
SOX2
|
SRY (sex determining region Y)-box 2
|
|
SOX9
|
SRY (sex determining region Y)-box 9
|
|
SUMF1
|
sulfatase modifying factor 1
|
