fragile skeleton Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000061
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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