Sirenomelia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A developmental defect in which the legs are fused together. (Human Phenotype Ontology, HP_0010497)
External Link https://www.disgenet.org/browser/0/1/0/C0037205
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Genes

11 genes associated with the disease Sirenomelia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AKT1 v-akt murine thymoma viral oncogene homolog 1
BMP7 bone morphogenetic protein 7
CYP26A1 cytochrome P450, family 26, subfamily A, polypeptide 1
DACT1 dishevelled-binding antagonist of beta-catenin 1
FGF20 fibroblast growth factor 20
GREB1L growth regulation by estrogen in breast cancer-like
ITGA8 integrin, alpha 8
PTEN phosphatase and tensin homolog
RET ret proto-oncogene
SGPL1 sphingosine-1-phosphate lyase 1
TBC1D24 TBC1 domain family, member 24