fragile skeleton Gene Set
Genes
23 gene mutations causing the fragile skeleton phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
AKR1A1
|
aldo-keto reductase family 1, member A1 (aldehyde reductase)
|
|
ALPL
|
alkaline phosphatase, liver/bone/kidney
|
|
COL1A1
|
collagen, type I, alpha 1
|
|
COL1A2
|
collagen, type I, alpha 2
|
|
CREB3L1
|
cAMP responsive element binding protein 3-like 1
|
|
CSF1
|
colony stimulating factor 1 (macrophage)
|
|
CSF1R
|
colony stimulating factor 1 receptor
|
|
CTSK
|
cathepsin K
|
|
FAM20C
|
family with sequence similarity 20, member C
|
|
FGF23
|
fibroblast growth factor 23
|
|
GLRB
|
glycine receptor, beta
|
|
HAX1
|
HCLS1 associated protein X-1
|
|
ID1
|
inhibitor of DNA binding 1, dominant negative helix-loop-helix protein
|
|
MYOG
|
myogenin (myogenic factor 4)
|
|
PHOSPHO1
|
phosphatase, orphan 1
|
|
PRPSAP2
|
phosphoribosyl pyrophosphate synthetase-associated protein 2
|
|
RGN
|
regucalcin
|
|
SLC38A10
|
solute carrier family 38, member 10
|
|
SPARC
|
secreted protein, acidic, cysteine-rich (osteonectin)
|
|
SUCO
|
SUN domain containing ossification factor
|
|
TNFRSF11B
|
tumor necrosis factor receptor superfamily, member 11b
|
|
UROS
|
uroporphyrinogen III synthase
|
|
ZMPSTE24
|
zinc metallopeptidase STE24
|
