aplasia/hypoplasia of the vertebrae Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008515
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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